Next Article in Journal
Assessment and Impact of Cognitive Impairment in Multiple Sclerosis: An Overview
Next Article in Special Issue
The Role of Wnt and R-spondin in the Stomach During Health and Disease
Previous Article in Journal
Monoclonal Antibodies in Multiple Sclerosis: Present and Future
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Biomedicines
Volume 7
Issue 1
10.3390/biomedicines7010021
biomedicines-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Calcium Carbonate Nanoparticles Can Activate the Epithelial–Mesenchymal Transition in an Experimental Gastric Cancer Model

by
Marina Senchukova
1,*,
Olesya Tomchuk
2,
Elena Shurygina
3,
Sergey Letuta
4,5,
Eskender Alidzhanov
4,5,
Hike Nikiyan
4,5 and
Dmitry Razdobreev
4,5
1
Department of Oncology, Orenburg State Medical University, Orenburg 460000, Russia
2
Department of Histology, Cytology, Embryology, Orenburg State Medical University, Orenburg 460000, Russia
3
Department of Pathology, Orenburg State Medical University, Orenburg 460000, Russia
4
Department of Biophysics and Condensed Matter Physics, Orenburg State University, Orenburg 460018, Russia
5
Institute of micro- and nanotechnology, Orenburg State University, Orenburg 460018, Russia
*
Author to whom correspondence should be addressed.
Biomedicines 2019, 7(1), 21; https://doi.org/10.3390/biomedicines7010021
Submission received: 14 February 2019 / Revised: 14 March 2019 / Accepted: 15 March 2019 / Published: 19 March 2019
(This article belongs to the Special Issue Gastric Cancer Research: From Basic Science to the Clinic)
Browse Figures
Review Reports Versions Notes

Abstract

:
Previously, we have shown the possibility of intramucosal gastric carcinoma induction by the intragastric administration of a mixture of formaldehyde and hydrogen peroxide in rats. In this study, we report a sizable increase in carcinogenic properties of the mixture when a suspension containing calcium carbonate nanoparticles was added to it. This technique allowed us to reduce both the number of the carcinogen administrations from twelve to two and the time to the cancer induction from six to four months. Although the induced tumors were represented by the intramucosal carcinomas, they were characterized by the extensive invasion of individual tumor cells and their clusters into the muscle layer and serosa as well as into the omentum and blood vessels. Considering that the invasive tumor cells were positive for vimentin, Snail and TGF-β2, we concluded that their invasion was the result of the activation of epithelial–mesenchymal transition (EMT) mechanisms. Thus, taking into account the data obtained, it can be assumed that under the conditions of inflammation or carcinogenesis, the calcium carbonate nanoparticles may affect the activation of EMT mechanisms.

Graphical Abstract

1. Introduction

Gastric cancer (GC) is the fifth most common cancer in the world and has the third highest mortality rate [1,2]. Most cases of GC are diagnosed at an advanced stage with metastasis, and thus have poor prognosis [2,3]. In this regard, studying the mechanisms of GC progression is an urgent task and experimental modeling plays an important role.
According to modern concepts, epithelial–mesenchymal transition (EMT) is a crucial process for malignant tumors metastasis which is still the major cause of cancer-related deaths [4,5]. The inducers of EMT may be act hypoxia, oxidative stress, inflammation and other factors [6]. Recently, it has been shown that nanoparticles (NPs) can also stimulate metastasis [7], by increasing the level of TGF-β, one of the key EMT inducers [8]. Within this context, the role of NPs in tumor progression is being studied with increased intensity.
Calcium carbonate (CaCO3) is the very abundant mineral in nature. Calcium carbonate-based nanomaterials are widely used in the food and pharmaceutical industries. In a number of studies the cytotoxic effect of CaCO3 NPs was noted [9,10], but the probability of its influence to tumor progression was not examined.
Previously, we have shown the potential of GC induction by intragastric administration of a mixture of formaldehyde (FA) and hydrogen peroxide (HP) in white outbred rats. The animals were given a 1.0 mL mixture of 0.4% FA and 0.4% HP (1:1) by oral gavage on the first and third day every two weeks for six months [11]. Further development of this technology led to the creation of a new experimental model of GC with some interesting features associated with EMT.

2. Methods and Materials

2.1. Animals and Housing

Wistar male rats, 1.5–2.0 months in age and weighing 200–250 g, were supplied by Rappolovo (Leningrad region, Russia). Five animals per cage were housed in the animal facility of Orenburg State Medical University in an air-conditioned room with a 12 h light/dark cycle at 21–22 °C, and were provided ad libitum with a standard commercial rodent food and water.

2.2. Ethics Statement

All experiments and procedures were approved by the Institutional Animal Care Committee of Orenburg State Medical University (application No. 105, approved on 1 October 2014). All animal experiments were performed in accordance with the Guidelines for the Care and Use of Laboratory Animals for Scientific Purposes. All efforts were made to minimize discomfort in these noninvasive procedures.

2.3. Experimental Design

Animals were divided into 2 groups, experimental (n = 15) and control (n = 3). In order to induce GC, the rats were given 1.0 mL of a suspension of CaCO3 at a concentration 0.05% in a 1:1 (v/v) mixture with 0.4% FA and 0.4% HP, by oral gavage on the 1st and 3rd day of the experiment. The suspension was prepared by adding 10 g of CaCO3 to 40% FA to a final volume of 100 mL. One mL of this suspension was diluted with 99 mL distilled water and this was then mixed in a 1:1 (v/v) ratio with a 0.4% solution of HP (2 mL of 3% HP + 13 mL of the distilled water). The resulting solution was administered to animals for 15–20 min. The control animals were given 1.0 mL distilled water in a similar manner and at the same time. Five experimental rats and one control rat were sacrificed at 16 weeks, and the remaining 9 experimental and 2 control rats were sacrificed at 24 weeks. Rats were euthanized using ether vapor. A thorough necropsy of each rat was made, and the entire gastrointestinal tract was scrutinized for lesions. The stomach was opened along the greater curvature and carefully examined. On laparotomy, the organs were also examined for possible metastasis. The number, size and location of lesions were documented.

2.4. Histological and Histochemical Assay

The specimens of gastric lesions with the adjacent mucosal tissues were fixed in 10% neutral buffered formalin for up to 24 h and embedded in paraffin. Sections of 3–5 µm thickness were then cut from the paraffin blocks and stained with Mayer’s hematoxylin and eosin (H&E).
To image calcium deposits in sections, the von Kossa (calcium stain) technique was used (Abcam, Cambridge, MA, USA), according to the manufacturer’s protocol. Sections were deparaffinized in toluene and hydrated by serial washing in graded ethanol and distilled water. Next, the sections were exposed to 3% silver nitrate under ultraviolet light for 30 min, followed by careful washing with distilled water 2 times. Thereafter, the sections were treated with 5% sodium thio-sulfate for 2–3 min, washed thoroughly with distilled water, counterstained with nuclear fast red solution for 5 min and dehydrated in the usual manner. Histological slides were studied by light microscopy, with an Optika B-350 microscope, connected to a ScopeTek DCM500 camera (Optika Srl, Ponteranica, Italy).

2.5. Immunohistochemistry

For immunohistochemistry (IHC), 4-µm sections were dewaxed, hydrated and heat-treated in 1 mM EDTA pH 8 in an antigen retrieval PT module (Thermo Fisher Scientific Inc., Waltham, MA, USA) at 95 °C for 20 min. Sections were then stained with the following antibodies: Rabbit monoclonal antibody to vimentin (Clone SP20) 1:200 dilution (Spring Bioscience Corp., Pleasanton, CA, USA); goat polyclonal antibody to Snail (ab53519), 1:200 dilution (Abcam, Cambridge, MA, USA); mouse monoclonal antibody against TGF-β2 (220ct16.4.3.1), 1:40 dilution (Cell Marque Corp., Rocklin, CA, USA). The staining procedure was performed according to the manufacturers’ protocols using an Autostainer 480 (Thermo Fisher Scientific Ltd., Vantaa, Finland). The visualization system included UltraVision LP Detection System HRP Polymer & DAB Plus Chromogen (Thermo Fisher Scientific Inc., Waltham, MA, USA) and hematoxylin counterstaining. For the negative control sections, primary antibodies were replaced with phosphate-buffered saline and processed in the same manner. Stained slides were evaluated by two pathologists (MS and OT). The number of Snail and TGF-β2 positive cells was counted in 10 randomly selected fields by light microscopy at 400× magnification. The percentage of positive cells was expressed relative to the total number of tumor or epithelial cells counted.

2.6. Detection and Characterization of Calcium Carbonate Nanoparticles

The sizes and the proportion of nanoparticles (NPs) in the working solution were determined by dynamic light scattering (DLS) on the Photocor Compact-Z analyzer (Photokor Ltd., Moscow, Russia). Before the measurements, the working solution was filtered using a Vladipor membrane filter (MFAS-OC-2 series; ZAO STC “Vladipor”, Moscow, Russia) with a pore size of 450 nm and was placed in a quartz cuvette measuring 1 × 1 × 3 cm for testing. The measurements were carried out at room temperature in manual mode at a scattering angle of 90°. A total of 56 measurements of working solution samples were made.
The morphologic and particle size examination of CaCO3 NPs was conducted by SMM-2000 atomic force microscopy (JSC “Proton-MIET Plant”, Moscow, Russia) operated in contact mode. V-shaped silicon nitride cantilevers (MSCT; Bruker Corp., Billerica, MA, USA) with a spring constant of 0.01 N/m and 10 nm tip radius were used.
Ten μL of the suspension of CaCO3 in a mixture of FA and HP was applied to a fresh shear of mica. It was left for a day until the solvents had completely evaporated, after which scanning was performed.

2.7. Statistics

STATSTICA 6.0 software (StatSoft Inc, Tulsa, OK, USA) was employed and all data are presented as means ± standard deviation (SD) or medians. Student’s t-test was performed for comparisons between two groups. A value of p < 0.05 was considered statistically significant.

3. Results

The mortality rate among treated rats was 6.7%. Four months from the beginning of treatment, 4 out of 5 rats in the experimental group had gastric tumors, while after 6 months all 9 experimental rats showed malignant tumors of the stomach. The tumors were represented by intramucosal carcinomas and observed only in the stomach body. Macroscopically, the gastric lesions looked like a diffuse thickening of the organ wall. In most cases, multifocal damage of the organ was found. Nodal indurations of gray color were also often observed on the gastric visceral peritoneum and in the omentum. At these times, formation of tumors was not noted in comparable controls.

3.1. Pathology of the Gastric Tumor

In accordance with the Vienna classification, all changes detected in the stomach corresponded to gastrointestinal epithelial neoplasia [12]. However, the lesions in the pre-stomach and in the glandular stomach had a different character, as follows.
In the forestomach, there was an increase of thickness and the number of epidermal rows, mainly at the expense of the basal and spinous layers. Here, polymorphic chaotically located cells with many mitotic figures were observed in large numbers. These changes were most evident in the area of the groove between the rat forestomach and glandular stomach (Figure 1a,b) and corresponded to low grade gastric dysplasia (Category 3 in the Vienna Classification of epithelial neoplasia [12]).
In the stomach body, the lesions corresponding to intramucosal carcinomas (Category 5 in the Vienna Classification of epithelial neoplasia [12]) were observed. The changes mainly affected the basal parts of gastric glands, where areas with marked cytological and architectural atypia were observed. In these areas, the cystic-distorted glands (Figure 2a) often with proliferations of atypical epithelium in their lumen (Figure 2b) were found. These glandular-like structures were lined by flattened polymorphic cells with hyperchromic nuclei of irregular shape and with а large number of bizarre mitotic figures, as well as a markedly increased nuclear/cytoplasmic ratio. These cells were positive for Snail and TGF-β2 (Figure 2c,d). In control animals the single Snail positive cells in the muscle plate and the weak TGF-β2 expression in the chief cells of the gastric glands were observed (Figure 2e,f), which corresponds to results obtained by other authors [13].
The density of Snail positive cells and TGF-β2 positive cells in the lining of the cystic-distorted glands and in the normal gastric glands was 12.5 ± 8.7% and 0% (p < 0.01), and 100% and 24.7 ± 16.4% (p < 0.001), respectively. In adjacent tissue, the invasion of curved basophilic fibroblast-like cells in the muscle plate and gastric submucosa was noted. These cells were positive for vimentin and Snail.
In the pyloric glands, the dysplastic changes were more marked in the generative zone of gastric glands, where the ones were lined by prismatic cells with large polymorphic nuclei, having irregular hyperchromatism and irregular nucleoli as well as increased mitotic figures (Figure 3a). Dysplastic changes in the pyloric glands were characterized by the appearance of light vacuoles in the cells. In some areas, the glands were lined by cells with large cytoplasmic mucus vacuoles and hyperchromatic and depolarized nuclei (somewhat resembling signet ring cells), and these were positive for staining with Snail antibodies (Figure 3b). The described changes corresponded to high grade dysplasia (Category 4 in the Vienna Classification of epithelial neoplasia [12]).
The main feature that enabled the classification of relevant changes as malignant tumors, corresponding to intramucosal gastric carcinoma, was the presence of tumor emboli in vessels (Figure 4a) as well as cords and clusters of tumor cells in the muscle layer (Figure 4b), the serosa (Figure 4c), and the omentum (Figure 4d). In these structures, cells of three types were observed: Fibroblast-like cells with a curved shape; cells of oval or polygonal shape with finely dispersed oxyphilic inclusions in the cytoplasm and a small, rounded, centrally located nucleus (Figure 4e); and cells with large, polymorphic, hyperchromic nuclei and with a markedly increased nuclear/cytoplasmic ratio (Figure 4f).
Immunohistochemistry demonstrated that vimentin (Figure 5a,b), Snail (Figure 5c,d) and TGF-β2 (Figure 5e,f) positive cells were detected in the described structures.
Six months from the beginning of the experiment, two rats had cecum cancer consistent with well-differentiated adenocarcinoma (Figure 6a,b). In four animals, dense lymph nodes were also detected in the mesentery, in the area of the ileocecal angle. Lymph nodes were increased to 0.5–1.2 cm in diameter, but we did not reveal obvious histological signs of their metastatic lesion.
When samples were stained by the von Kossa technique, multiple microcalcifications were revealed in the gastric mucosa of animals from the experimental group, even six months after the beginning of the experiment. The largest number of microcalcifications was observed in stomach body and antrum. Microcalcifications had various shapes and sizes (Figure 7a). Separate crystals were also found in the gastric submucosa. Microcalcifications were not found in the gastric mucosa of the control group of rats (Figure 7b).

3.2. Dynamic Light Scattering (DLS) Analysis of the Carcinogenic Suspension for the Presence and Morphology of Calcium Carbonate Nanoparticles

Analysis showed that CaCO3 NPs were presented in the carcinogenic suspension. An example histogram, showing the distribution of CaCO3 NPs according to their hydrodynamic radii obtained by the DLS method, is shown in Figure 7c.
The NPs with radius of 0.12–37.9 nm (average radius 7.8 ± 10.8 nm; median 0.42 nm) were found in 0.2%–12.2% (3.1% ± 2.6%; median 2.3%) of all particles dispersed in solution, and with radius of 47.0–267.2 nm (average radius 155.3 ± 86.5; median 66.5) were found in 0.14%–75.5% (16.8% ± 15.4%; median 12.4%) of all particles dispersed in solution.

3.3. Atomic Force Microscopic (AFM) Analysis of the Carcinogenic Suspension for the Presence and Morphology of Calcium Carbonate Nanoparticles

Images obtained by AFM showed the presence of CaCO3 NPs with spherical or oval shapes (Figure 7d). Both individual NPs and their aggregates were observed in the carcinogenic suspension.

4. Discussion

The study of the mechanisms associated with metastasis of malignant tumors is of fundamental importance for predicting the risk of metastasis, its prevention and its successful treatment. The solution to this problem is impossible without the development of effective experimental models that best reflect these mechanisms.
We have previously reported on the feasibility of GC induction by using a mixture of FA and HP [11]. For tumor induction, 1.0 mL a mixture of 0.4% FA and 0.4% HP (1:1 v/v) were administered to rats using intragastric gavage on the first and third day every two weeks for six months. Six months after the onset of treatment, tumors were observed in 80% of the animals, and after 7.5 months in all survived rats. Initiated tumors were corresponded to intramucosal carcinoma and characterized by invasion of individual tumor cells and their clusters in muscle and serous layer and in omentum, and by the presence of tumor emboli in vessels. These data conformed with results of some clinical studies, showing that gastric high-grade dysplasia can be associated with submucosal and lymphovascular invasion [14,15].
The idea of using a mixture of FA and HP to induce GC was based on published data indicating the mutagenic and carcinogenic properties of these substances. In particular, the administration of FA to drinking water for two years led to the appearance of malignant lymphomas and tumors of the gastrointestinal tract in experimental animals [16]. The carcinogenic effect of FA is likely associated with its genotoxic properties and the ability to form DNA–protein cross-links [17,18]. Genotoxic properties and the ability to stimulate neoangiogenesis have been also noted for HP [19,20,21]. When HP and FA are used together their mutagenic properties have been shown to increase [22]. This increase may be due to a number of interesting chemical properties. Serebrennikov and Golovkin (2005) reported that the starting products of FA and HP reaction as well as their complexes were stable in the mixture for a long time [23]. Regardless of the mixed substances ratio (1:1, 1:2 or 2:1), the intermediate and relatively resistant product of their reaction is the peroxide molecule H2C(OH)OOH. Later this molecule decomposes to formic acid, water and carbon dioxide.
In the current study, we presented a new experimental model for GC that was developed as a result of controlled changes in the methodology described above. The proposed model was conformed the intramucosal gastric carcinoma with invasion of tumor cells in the gastric submucosa, the muscular layer, serosa and omentum, as well as tumor emboli in the vessels. We believe that the results of the experiment are consistent with the Klein hypothesis that suggested tumor growth and metastasis could proceed in parallel, independently of each other [24]. In addition, the received results lent legitimacy to the point of view of Japanese pathologists, who consider the severe dysplasia based on nuclear and structural atypia was cancer regardless of the presence of invasion [15,25].
Considering that the invasive tumor cells were positive for vimentin, Snail and TGF-β2, we concluded that their invasion is the result of activation of EMT mechanisms. EMT is a transdifferentiation process in which epithelial cells lose their cell–cell contacts and polarity and acquire mesenchymal properties, coupled to the ability to migrate and to invade the surrounding tissues [26,27]. The activation of EMT occurs under the influence of transforming growth factor beta (TGF-β) that is crucial to the regulation of cell proliferation, differentiation, invasion, migration and cancer metastasis [28]. The induction of EMT entails a reduction or loss of the ability to synthesize cytokeratins and E-cadherin by the epithelial and tumor cells, but the appearance of the ability to synthesize vimentin, Snail, smooth-muscle actin and other markers of EMT as well as an increasing expression of the genes encoding matrix metalloproteinases. As a result of EMT, cell–cell contacts are ruptured, cell morphology changes to fibroblast-like and the cells become mobile [27,29,30]. Additionally, in the process of EMT tumor cells acquire the properties of stem cancer cells, which are associated with high aggressiveness and drug resistance of malignant tumors [31,32].
We think that in interpreting the current experiment, the data of Ke et al. (2008) [33] should also be taken into account. They demonstrated that EMT processes are similar, but not identical, to malignant transformation. As such, they argued that a more strict confirmation is required that cell invasion is the result of not only EMT, but also their malignant transformation. In cases of gastric mucosa intraepithelial lesions, the differential diagnosis between a high degree of dysplasia and cancer presents known difficulties [14,34].
One of the principle results of our study was a sizable increase in the carcinogenic properties of the mixture of FA and HP when suspension containing CaCO3 NPs was added to it. The change in the experiment methodology allowed us to reduce the number of administrations of the carcinogen from 12 to two and in a shorter period of time to obtain a new experimental model of intramucosal gastric carcinoma, which was associated with activation of EMT mechanisms.
It should be noted that studying the role of NPs in the development of various diseases is receiving marked attention. It is known that NPs can not only cause chronic inflammatory and autoimmune diseases, but also malignant neoplasms [35,36,37]. Moreover, NPs can influence the mechanisms of tumor progression by stimulating the growth of metastases [7,38,39]. NPs in the size range 50–270 nm are the most dangerous in terms of producing pathological conditions [40]. These sizes allow NPs to easily penetrate between the epithelial cells into the underlying tissues, into the cells and vessels, as well as into the extracellular matrix. Macrophages, lymphoid and dendritic cells are capable of spreading the NPs beyond the sites of primary deposition. Inside cells, the NPs damage mitochondria and can penetrate into the nucleus of cells, causing DNA breakage [41]. In our experiment, when staining the stomach samples by the von Kossa method, we also observed microcalcifications in the cells and the intercellular substance of the gastric mucosa, even six months after the carcinogenic suspension administration (see Figure 7a,b).
The toxicity of NPs is explained by their physicochemical properties, the catalytic activity of the NP surface and their ability to penetrate through the lungs, skin, gastrointestinal tract into any human organ and tissue, including the central nervous system [42]. The main physicochemical properties of NPs determining their toxicity are absorption, distribution, toxicokinetics, metabolism, and features of their biodegradation. The biological activity of NPs also depends on their size, shape, and surface properties, such as their charge and catalytic properties. A number of authors have shown that the size of NPs is identical to those of signaling molecules and cellular receptors. In addition, nanoparticle sizes correspond to exosome sizes playing an important role in intracellular communication and in delivering molecular signals from one cell to another [43]. The contact of NPs with immune cells results in the following effects:
  • Increased synthesis of pro-inflammatory cytokines NF-κB (nuclear factor kappa B), IL-6 (interleukin 6), TNF-α (tumor necrotic factor-α) and IL-2 [44,45];
  • release of large concentrations of reactive oxygen and nitric oxide with the properties of free radicals that damage cell membranes and genetic material [44,45];
  • development of immunological tolerance due to the increase of TGF-β1serum levels [35,39,44];
  • generation of CD4+CD25+FoxP3+ regulatory T-cells [46,47,48] and the PD-L1 activation [49,50]. Considering that NPs used in the experiments had different chemical composition, it can be assumed that these properties may be associated not only with their structure, but, first of all, their size.
It is important to emphasize that that TGF-β, being one of the key activators of EMT, induces pro-invasive and pro-metastatic immune responses by the cooperation with stem cell pathways, such as Wnt and Ras signaling [51,52]. In addition, TGF-β plays a key role in the development of immunological tolerance. The cytokine inhibits the differentiation of cytotoxic T-lymphocytes, Th1 and Th2 cells, and stimulates the formation of peripheral Treg, Th17, Th9 and Tfh cells in response to various immune stimuli [53]. Increased expression of TGF-β is noted in various inflammatory, autoimmune and oncological diseases [53,54].
Once again, we note that CaCO3 is a very abundant mineral in nature. Calcium carbonate-based nanomaterials are widely used in the food and pharmaceutical industries. Some authors noted its very low toxicity during oral administration [55]. However, other researchers have shown its potential cytotoxicity. Kim (2015) demonstrated the calcifying NPs cytotoxicity when they were co-cultivated with different cell cultures [10]. The cytotoxicity was manifested by the NPs endocytosis, the production of intracellular reactive oxygen species, the membrane damage and cell apoptosis [56]. Similar results were obtained by Horie [9].
We believe that it is also necessary to note a number of other interesting features of CaCO3 NPs. In particular, CaCO3 is the main mineral element of mineral-organic NPs that were described in detail by Martel and Young [57]. These NPs have been established to form in human biological fluids when the concentration of CaCO3 and phosphate ions exceeds saturation. Contact of crystalline CaCO3 (both endogenous and exogenous) with biological fluids like serum leads to the formation of round amorphous NPs [58,59,60] that had earlier been misconstrued as nanobacteria [61]. Described NPs are found in different human biological fluids, and their presence is associated with various pathological processes, including Alzheimer’s disease, atherosclerosis, cancer, kidney stones, prostatitis and others [58,59,60]. In inflammation the high concentration of mineral-organic NPs in biological fluids can lead to ectopic calcification [58].
Powell (2015) described the mechanism of the endogenous formation of calcium containing mineral-organic NPs [62]. They showed that calcium and phosphate ions are secreted from the distal small intestine into the lumen and then react with exogenous and endogenous proteins with the formation of mineral-organic NPs in the intestinal lumen. These proteins transport them to immune cells of intestinal tissue. In wild-type mice, intestinal immune cells containing these naturally formed NPs expressed the immune tolerance-associated molecule PD-L1. The authors suggest that the described mechanism participates in the formation of immunological tolerance against food and the gut microbiota. Given that mineral-organic NPs play a key role in ectopic calcification [58,59,60], it can be assumed that extra-bone calcification, which is observed from atrophic, dystrophic, dysplastic and necrobiotic changes in tissues, as well as in benign and malignant tumors [63,64,65,66,67,68,69], can also be associated with the activation of the immunological tolerance mechanisms. The fact that the same cytokines and mediators are involved both in the processes associated with extracellular calcification and in the development of immunological tolerance [68,69] indirectly supports this assumption

5. Conclusions

Taking into account the data obtained and the analysis data of the scientific literature, it can be assumed that under the conditions of inflammation or carcinogenesis, the CaCO3 NPs may affect the activation of mechanisms of EMT and immunological tolerance. We believe that further research in this direction is necessary, since knowledge of these mechanisms may be of fundamental importance for the development of new approaches to the treatment and prevention of various diseases, including malignant neoplasms.

Author Contributions

M.S. designed the research, performed statistical analysis, interpreted data and was the primary manuscript writer; O.T. carried out the experiment and helped in data interpretation; E.S. performed the immunohistochemistry assays and helped in data interpretation; S.L., E.A., H.N. and D.R. studied the size and morphology of nanoparticles, helped in data analysis and its interpretation. All authors discussed the results and contributed to the final manuscript.

Funding

This research was funded by Russian Foundation for Basic Research and the government of the region of the Russian Federation, grant No. 18-415-560005.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ferlay, J.; Soerjomataram, I.; Dikshit, R.; Eser, S.; Mathers, C.; Rebelo, M.; Parkin, D.M.; Forman, D.; Bray, F. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int. J. Cancer. 2015, 136, 359–386. [Google Scholar] [CrossRef] [PubMed]
  2. Torre, L.A.; Bray, F.; Siegel, R.L.; Ferlay, J.; Lortet-Tieulent, J.; Jemal, A. Global cancer statistics, 2012. CA Cancer J. Clin. 2015, 65, 87–108. [Google Scholar] [CrossRef] [PubMed]
  3. Chen, X.L.; Zhao, L.Y.; Xue, L.; Xu, Y.H.; Zhang, W.H.; Liu, K.; Chen, X.Z.; Yang, K.; Zhang, B.; Chen, Z.X.; et al. Prognostic significance and the role in TNM stage of extranodal metastasis within regional lymph nodes station in gastric carcinoma. Oncotarget 2016, 7, 67047–67060. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Wei, S.; Wang, L.; Zhang, L.; Li, B.; Li, Z.; Zhang, Q.; Wang, J.; Chen, L.; Sun, G.; Li, Q.; et al. ZNF143 enhances metastasis of gastric cancer by promoting the process of EMT through PI3K/AKT signaling pathway. Tumour Biol. 2016, 37, 12813–12821. [Google Scholar] [CrossRef] [PubMed]
  5. Zhao, W.; Jia, L.; Kuai, X.; Tang, Q.; Huang, X.; Yang, T.; Qiu, Z.; Zhu, J.; Huang, J.; Huang, W.; et al. The role and molecular mechanism of Trop2 induced epithelial-mesenchymal transition through mediated β-catenin in gastric cancer. Cancer Med. 2019. [Google Scholar] [CrossRef] [PubMed]
  6. Ricciardi, M.; Zanotto, M.; Malpeli, G.; Bassi, G.; Perbellini, O.; Chilosi, M.; Bifari, F.; Krampera, M. Epithelial-to-mesenchymal transition (EMT) induced by inflammatory priming elicits mesenchymal stromal cell-like immune-modulatory properties in cancer cells. Br. J. Cancer. 2015, 112, 1067–1075. [Google Scholar] [CrossRef] [Green Version]
  7. Wang, P.; Voronkova, M.; Luanpitpong, S.; He, X.; Riedel, H.; Dinu, C.Z.; Wang, L.; Rojanasakul, Y. Induction of Slug by Chronic Exposure to Single-Walled Carbon Nanotubes Promotes Tumor Formation and Metastasis. Chem. Res. Toxicol. 2017, 30, 1396–1405. [Google Scholar] [CrossRef]
  8. Shvedova, A.A.; Kisin, E.R.; Yanamala, N.; Tkach, A.V.; Gutkin, D.W.; Star, A.; Shurin, G.V.; Kagan, V.E.; Shurin, M.R. MDSC and TGFβ Are Required for Facilitation of Tumor Growth in the Lungs of Mice Exposed to Carbon Nanotubes. Cancer Res. 2015, 75, 1615–1623. [Google Scholar] [CrossRef]
  9. Horie, M.; Nishio, K.; Kato, H.; Endoh, S.; Fujita, K.; Nakamura, A.; Kinugasa, S.; Hagihara, Y.; Yoshida, Y.; Iwahashi, H. Evaluation of cellular influences caused by calcium carbonate nanoparticles. Chem. Biol. Interact. 2014, 210, 64–76. [Google Scholar] [CrossRef]
  10. Kim, M.K.; Lee, J.A.; Jo, M.R.; Kim, M.K.; Kim, H.M.; Oh, J.M.; Song, N.W.; Choi, S.J. Cytotoxicity, Uptake Behaviors, and Oral Absorption of Food Grade Calcium Carbonate Nanomaterials. Nanomaterials 2015, 5, 1938–1954. [Google Scholar] [CrossRef] [Green Version]
  11. Senchukova, M.A.; Stadnikov, A.A.; Kozlov, A.A.; Bokov, D.A. Method of the Experimental Gastric Cancer Modeling. Patent for the Invention RU 2401463, 2009. (In Russian). [Google Scholar]
  12. Schlemper, R.J.; Riddell, R.H.; Kato, Y.; Borchard, F.; Cooper, H.S.; Dawsey, S.M.; Dixon, M.F.; Fenoglio-Preiser, C.M.; Fléjou, J.F.; Geboes, K.; et al. The Vienna classification of gastrointestinal epithelial neoplasia. Gut 2000, 47, 251–255. [Google Scholar] [CrossRef] [Green Version]
  13. De Andrade Sá, E.R.; Jordão, L.R.; Takahashi, C.A.; Alvares, E.P.; Gama, P. Ontogenic expression of TGFbeta 1, 2, and 3 and its receptors in the rat gastric mucosa. Dev. Dyn. 2003, 227, 450–457. [Google Scholar] [CrossRef]
  14. Sakurai, U.; Lauwers, G.Y.; Vieth, M.; Sawabe, M.; Arai, T.; Yoshida, T.; Aida, J.; Takubo, K. Gastric high-grade dysplasia can be associated with submucosal invasion: Evaluation of its prevalence in a series of 121 endoscopically resected specimens. Am. J. Surg. Pathol. 2014, 38, 1545–1550. [Google Scholar] [CrossRef]
  15. Gurzu, S.; Sugimura, H.; Orlowska, J.; Szentirmay, Z.; Jung, I. New Insights in Histogenetic Pathways of Gastric Cancer. Medicine 2015, 94, e1810. [Google Scholar] [CrossRef] [Green Version]
  16. Soffritti, M.; Belpoggi, F.; Lambertin, L.; Lauriola, M.; Padovani, M.; Maltoni, C. Results of long-term experimental studies on the carcinogenicity of formaldehyde and acetaldehyde in rats. Ann. N. Y. Acad. Sci. 2002, 982, 87–105. [Google Scholar] [CrossRef]
  17. Neuss, S.; Speit, G. Further characterization of the genotoxicity of formaldehyde in vitro by the sister chromatid exchange test and co-cultivation experiments. Mutagenesis 2008, 23, 355–357. [Google Scholar] [CrossRef] [Green Version]
  18. Speit, G.; Schmid, O.; Neuss, S.; Schütz, P. Genotoxic effects of formaldehyde in the human lung cell line A549 and in primary human nasal epithelial cells. Environ. Mol. Mutagen. 2008, 49, 300–307. [Google Scholar] [CrossRef]
  19. Andersson, M.; Stenqvist, P.; Hellman, B. Interindividual differences in initial DNA repair capacity when evaluating H2O2-induced DNA damage in extended-term cultures of human lymphocytes using the comet assay. Cell Biol. Toxicol. 2007, 23, 401–411. [Google Scholar] [CrossRef]
  20. Horváthová, E.; Slamenová, D.; Marsálková, L.; Sramková, M.; Wsólová, L. Effects of borneol on the level of DNA damage induced in primary rat hepatocytes and testicular cells by hydrogen peroxide. Food Chem. Toxicol. 2009, 47, 1318–1323. [Google Scholar] [CrossRef]
  21. Kim, Y.M.; Kim, K.E.; Koh, G.Y.; Ho, Y.S.; Lee, K.J. Hydrogen peroxide produced by angiopoietin-1 mediates angiogenesis. Cancer Res. 2006, 66, 6167–6174. [Google Scholar] [CrossRef]
  22. Lin, Z.; Luo, W.; Li, H.; Zhang, Y. The effect of endogenous formaldehyde on the rat aorta endothelial cells. Toxicol. Lett. 2005, 159, 134–143. [Google Scholar] [CrossRef]
  23. Serebrennikov, L.V.; Golovkin, A.V. The reaction between formaldehyde and hydrogen peroxide. IR-spectra in xenon matrixes and calculations of intermediates and transition states. Bull. Moscow Univ. Ser. 2 Chem. 2005, 6, 370–377. [Google Scholar]
  24. Klein, C.A. Parallel progression of primary tumours and metastases. Nat. Rev. Cancer 2009, 9, 302–312. [Google Scholar] [CrossRef]
  25. Japanese Research Society for Gastric Cancer. Japanese Classification of Gastric Carcinoma; Kanehara & Co., Ltd.: Tokyo, Japan, 1995.
  26. Bhatia, S.; Monkman, J.; Toh, A.K.L.; Nagaraj, S.H.; Thompson, E.W. Targeting epithelial-mesenchymal plasticity in cancer: Clinical and preclinical advances in therapy and monitoring. Biochem. J. 2017, 474, 3269–3306. [Google Scholar] [CrossRef]
  27. Santamaria, P.G.; Moreno-Bueno, G.; Portillo, F.; Cano, A. EMT: Present and future in clinical oncology. Mol. Oncol. 2017, 11, 718–738. [Google Scholar] [CrossRef] [Green Version]
  28. Akhurst, R.J.; Padgett, R.W. Matters of context guide future research in TGFβ superfamily signaling. Sci. Signal. 2015, 8, re10. [Google Scholar] [CrossRef]
  29. Lee, H.; Pyo, M.J.; Bae, S.K.; Heo, Y.; Choudhary, I.; Hwang, D.; Yang, H.; Kim, J.H.; Chae, J.; Han, C.H.; et al. Nemopilema nomurai jellyfish venom exerts an anti-metastatic effect by inhibiting Smad- and NF-κB-mediated epithelial-mesenchymal transition in HepG2 cells. Sci. Rep. 2018, 8, 2808. [Google Scholar] [CrossRef]
  30. Lin, R.L.; Zhao, L.J. Mechanistic basis and clinical relevance of the role of transforming growth factor-β in cancer. Cancer Biol. Med. 2015, 12, 385–393. [Google Scholar] [CrossRef]
  31. Dave, B.; Mittal, V.; Tan, N.M.; Chang, J.C. Epithelial-mesenchymal transition, cancer stem cells and treatment resistance. Breast Cancer Res. 2012, 14, 202. [Google Scholar] [CrossRef]
  32. Yoon, C.; Cho, S.J.; Chang, K.K.; Park, D.J.; Ryeom, S.W.; Yoon, S.S. Role of Rac1 Pathway in Epithelial-to-Mesenchymal Transition and Cancer Stem-like Cell Phenotypes in Gastric Adenocarcinoma. Mol. Cancer Res. 2017, 15, 1106–1116. [Google Scholar] [CrossRef]
  33. Ke, X.S.; Qu, Y.; Goldfinger, N.; Rostad, K.; Hovland, R.; Akslen, L.A.; Rotter, V.; Øyan, A.M.; Kalland, K.H. Epithelial to mesenchymal transition of a primary prostate cell line with switches of cell adhesion modules but without malignant transformation. PLoS ONE 2008, 3, e3368. [Google Scholar] [CrossRef]
  34. Maekawa, A.; Kato, M.; Nakamura, T.; Komori, M.; Yamada, T.; Yamamoto, K.; Ogiyama, H.; Nakahara, M.; Kawai, N.; Yabuta, T.; et al. Incidence of gastric adenocarcinoma among lesions diagnosed as low-grade adenoma/dysplasia on endoscopic biopsy: A multicenter, prospective, observational study. Dig. Endosc. 2018, 30, 228–235. [Google Scholar] [CrossRef]
  35. Khaliullin, T.O.; Kisin, E.R.; Murray, A.R.; Yanamala, N.; Shurin, M.R.; Gutkin, D.W.; Fatkhutdinova, L.M.; Kagan, V.E.; Shvedova, A.A. Mediation of the single-walled carbon nanotubes induced pulmonary fibrogenic response by osteopontin and TGF-β1. Exp. Lung Res. 2017, 43, 311–326. [Google Scholar] [CrossRef]
  36. Dobrovolskaia, M.A.; Shurin, M.R.; Kagan, V.E.; Shvedova, A.A. Ins and Outs in Environmental and Occupational Safety Studies of Asthma and Engineered Nanomaterials. ACS Nano 2017, 11, 7565–7571. [Google Scholar] [CrossRef]
  37. Hobson, D.W.; Roberts, S.M.; Shvedova, A.A.; Warheit, D.B.; Hinkley, G.K.; Guy, R.C. Applied Nanotoxicology. Int. J. Toxicol. 2016, 35, 5–16. [Google Scholar] [CrossRef] [Green Version]
  38. Sargent, L.M.; Porter, D.W.; Staska, L.M.; Hubbs, A.F.; Lowry, D.T.; Battelli, L.; Siegrist, K.J.; Kashon, M.L.; Mercer, R.R.; Bauer, A.K.; et al. Promotion of lung adenocarcinoma following inhalation exposure to multi-walled carbon nanotubes. Part. Fibre Toxicol. 2014, 11, 3. [Google Scholar] [CrossRef]
  39. Shvedova, A.A.; Tkach, A.V.; Kisin, E.R.; Khaliullin, T.; Stanley, S.; Gutkin, D.W.; Star, A.; Chen, Y.; Shurin, G.V.; Kagan, V.E.; et al. Carbon nanotubes enhance metastatic growth of lung carcinoma via up-regulation of myeloid-derived suppressor cells. Small 2013, 9, 1691–1695. [Google Scholar] [CrossRef]
  40. Brown, D.M.; Wilson, M.R.; MacNee, W.; Stone, V.; Donaldson, K. Size-dependent proinflammatory effects of ultrafine polystyrene particles: A role for surface area and oxidative stress in the enhanced activity of ultrafines. Toxicol. Appl. Pharmacol. 2001, 175, 191–199. [Google Scholar] [CrossRef]
  41. Porter, D.W.; Hubbs, A.F.; Chen, B.T.; McKinney, W.; Mercer, R.R.; Wolfarth, M.G.; Battelli, L.; Wu, N.; Sriram, K.; Leonard, S.; et al. Acute pulmonary dose-responses to inhaled multi-walled carbon nanotubes. Nanotoxicology 2013, 7, 1179–1194. [Google Scholar] [CrossRef]
  42. Kermanizadeh, A.; Balharry, D.; Wallin, H.; Loft, S.; Møller, P. Nanomaterial translocation—The biokinetics, tissue accumulation, toxicity and fate of materials in secondary organs—A review. Crit. Rev. Toxicol. 2015, 45, 837–872. [Google Scholar] [CrossRef]
  43. Zhang, C.; Ji, Q.; Yang, Y.; Li, Q.; Wang, Z. Exosome: Function and Role in Cancer Metastasis and Drug Resistance. Technol. Cancer Res. Treat. 2018, 17, 1533033818763450. [Google Scholar] [CrossRef]
  44. Manke, A.; Wang, L.; Rojanasakul, Y. Mechanisms of nanoparticle-induced oxidative stress and toxicity. Biomed. Res. Int. 2013, 2013, 942916. [Google Scholar] [CrossRef]
  45. Shvedova, A.A.; Yanamala, N.; Kisin, E.R.; Tkach, A.V.; Murray, A.R.; Hubbs, A.; Chirila, M.M.; Keohavong, P.; Sycheva, L.P.; Kagan, V.E.; et al. Long-term effects of carbon containing engineered nanomaterials and asbestos in the lung: One year postexposure comparisons. Am. J. Physiol. 2014, 306, 172–182. [Google Scholar] [CrossRef]
  46. Stead, S.O.; Kireta, S.; McInnes, S.J.P.; Kette, F.D.; Sivanathan, K.N.; Kim, J.; Cueto-Diaz, E.J.; Cunin, F.; Durand, J.O.; Drogemuller, C.J.; et al. Murine and Non-Human Primate Dendritic Cell Targeting Nanoparticles for in Vivo Generation of Regulatory T-Cells. ACS Nano 2018, 12, 6637–6647. [Google Scholar] [CrossRef]
  47. Tomić, S.; Janjetović, K.; Mihajlović, D.; Milenković, M.; Kravić-Stevović, T.; Marković, Z.; Todorović-Marković, B.; Spitalsky, Z.; Micusik, M.; Vučević, D.; et al. Graphene quantum dots suppress proinflammatory T cell responses via autophagy-dependent induction of tolerogenic dendritic cells. Biomaterials 2017, 146, 13–28. [Google Scholar] [CrossRef]
  48. Pearson, R.M.; Casey, L.M.; Hughes, K.R.; Wang, L.Z.; North, M.G.; Getts, D.R.; Miller, S.D.; She, L.D. Controlled Delivery of Single or Multiple Antigens in Tolerogenic Nanoparticles Using Peptide-Polymer Bioconjugates. Mol. Ther. 2017, 25, 1655–1664. [Google Scholar] [CrossRef]
  49. McCarthy, D.P.; Yap, J.W.; Harp, C.T.; Song, W.K.; Chen, J.; Pearson, R.M.; Miller, S.D.; Shea, L.D. An antigen-encapsulating nanoparticle platform for TH1/17 immune tolerance therapy. Nanomedicine 2017, 13, 191–200. [Google Scholar] [CrossRef]
  50. Kuo, R.; Saito, E.; Miller, S.D.; Shea, L.D. Peptide-Conjugated Nanoparticles Reduce Positive Co-stimulatory Expression and T Cell Activity to Induce Tolerance. Mol. Ther. 2017, 25, 1676–1685. [Google Scholar] [CrossRef]
  51. Fuxe, J.; Karlsson, M.C. TGF-β-induced epithelial-mesenchymal transition: A link between cancer and inflammation. Semin. Cancer Biol. 2012, 22, 455–461. [Google Scholar] [CrossRef]
  52. Johansson, J.; Tabor, V.; Wikell, A.; Jalkanen, S.; Fuxe, J. TGF-β1-induced epithelial–mesenchymal transition promotes monocyte/macrophage properties in breast cancer cells. Front. Oncol. 2015, 5, 3. [Google Scholar] [CrossRef]
  53. Sanjabi, S.; Oh, S.A.; Li, M.O. Regulation of the Immune Response by TGF-β: From Conception to Autoimmunity and Infection. Cold Spring Harb. Perspect. Biol. 2017, 9. [Google Scholar] [CrossRef]
  54. Bjarnadóttir, K.; Benkhoucha, M.; Merkler, D.; Weber, M.S.; Payne, N.L.; Bernard, C.C.; Molnarfi, N.; Lalive, P.H. B cell-derived transforming growth factor-β1 expression limits the induction phase of autoimmune neuroinflammation. Sci. Rep. 2016, 6, 34594. [Google Scholar] [CrossRef] [Green Version]
  55. Jeong, M.S.; Cho, H.S.; Park, S.J.; Song, K.S.; Ahn, K.S.; Cho, M.H.; Kim, J.S. Physico-chemical characterization-based safety evaluation of nanocalcium. Food Chem. Toxicol. 2013, 62, 308–317. [Google Scholar] [CrossRef]
  56. Wu, J.H.; Deng, Y.L.; Liu, Q.; Yu, J.C.; Liu, Y.L.; He, Z.Q.; Guan, X.F. Induction of apoptosis and autophagy by calcifying nanoparticles in human bladder cancer cells. Tumour. Biol. 2017, 39, 1010428317707688. [Google Scholar] [CrossRef]
  57. Martel, J.; Young, J.D. Purported nanobacteria in human blood as calcium carbonate nanoparticles. Proc. Natl. Acad. Sci. USA 2008, 105, 5549–5554. [Google Scholar] [CrossRef] [Green Version]
  58. Wu, C.Y.; Martel, J.; Cheng, W.Y.; He, C.C.; Ojcius, D.M.; Young, J.D. Membrane vesicles nucleate mineralo-organic nanoparticles and induce carbonate apatite precipitation in human body fluids. J. Biol. Chem. 2013, 288, 30571–30584. [Google Scholar] [CrossRef]
  59. Wu, C.Y.; Martel, J.; Young, J.D. Comprehensive organic profiling of biological particles derived from blood. Sci. Rep. 2018, 8, 11310. [Google Scholar] [CrossRef]
  60. Martel, J.; Wu, C.Y.; Peng, H.H.; Young, J.D. Mineralo-organic nanoparticles in health and disease: An overview of recent findings. Nanomedicine 2018. [Google Scholar] [CrossRef]
  61. Kajander, E.O.; Ciftçioglu, N. Nanobacteria: An alternative mechanism for pathogenic intra- and extracellular calcification and stone formation. Proc. Natl. Acad. Sci. USA 1998, 95, 8274–8279. [Google Scholar] [CrossRef] [Green Version]
  62. Powell, J.J.; Thomas-McKay, E.; Thoree, V.; Robertson, J.; Hewitt, R.E.; Skepper, J.N.; Brown, A.; Hernandez-Garrido, J.C.; Midgley, P.A.; Gomez-Morilla, I.; et al. An endogenous nanomineral chaperones luminal antigen and peptidoglycan to intestinal immune cells. Nat. Nanotechnol. 2015, 10, 361–369. [Google Scholar] [CrossRef]
  63. Wong, T.Y.; Wu, C.Y.; Martel, J.; Lin, C.W.; Hsu, F.Y.; Ojcius, D.M.; Lin, P.Y.; Young, J.D. Detection and characterization of mineralo-organic nanoparticles in human kidneys. Sci. Rep. 2015, 5, 15272. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Stabley, J.N.; Towler, D.A. Arterial calcification in diabetes mellitus: Preclinical models and translational implications. Arterioscler. Thromb. Vasc. Biol. 2017, 37, 205–217. [Google Scholar] [CrossRef] [PubMed]
  65. Hino, R.; Motoi, N.; Toda, K.; Ebina, A.; Yamada, K.; Higuchi, M.; Hirokawa, M.; Ishikawa, Y. Stromal tiny black dots, like “sugar-coated”, of von Kossa stain is a diagnostic clue to hyalinizing trabecular tumor of the thyroid gland. Pathol. Int. 2018, 68, 176–182. [Google Scholar] [CrossRef] [PubMed]
  66. Li, C.; Cen, D.; Liu, Z.; Liang, C. Presence of Intratumoral Calcifications and Vasculature Is Associated With Poor Overall Survival in Clear Cell Renal Cell Carcinoma. J. Comput. Assist. Tomogr. 2018, 42, 418–422. [Google Scholar] [CrossRef]
  67. Scimeca, M.; Giannini, E.; Antonacci, C.; Pistolese, C.A.; Spagnoli, L.G.; Bonanno, E. Microcalcifications in breast cancer: An active phenomenon mediated by epithelial cells with mesenchymal characteristics. BMC Cancer 2014, 14, 286. [Google Scholar] [CrossRef] [PubMed]
  68. Park, S.; Lakatta, E.G. Role of inflammation in the pathogenesis of arterial stiffness. Yonsei Med. J. 2012, 53, 258–261. [Google Scholar] [CrossRef] [PubMed]
  69. Leopold, J.A. Vascular calcification: Mechanisms of vascular smooth muscle cell calcification. Trends Cardiovasc. Med. 2015, 25, 267–274. [Google Scholar] [CrossRef] [PubMed]
Biomedicines 07 00021 g001 550
Figure 1. The pathological changes in the forestomach. (a) Area of the groove between the forestomach and glandular stomach. Mayer’s hematoxylin and eosin (H&E) staining, scale bar 200 μm; (b) Increasing thickness and number of epidermal rows in the basal and spinous layers of forestomach. H&E staining, scale bar 100 μm.
Figure 1. The pathological changes in the forestomach. (a) Area of the groove between the forestomach and glandular stomach. Mayer’s hematoxylin and eosin (H&E) staining, scale bar 200 μm; (b) Increasing thickness and number of epidermal rows in the basal and spinous layers of forestomach. H&E staining, scale bar 100 μm.
Biomedicines 07 00021 g001
Biomedicines 07 00021 g002a 550Biomedicines 07 00021 g002b 550
Figure 2. The pathological changes in stomach body. (a) Basal part of gastric glands with marked cytological and architectural atypia (arrows). In the box the selected area is shown. H&E staining, scale bar 200 μm (in box—100 μm). (b) Proliferations of atypical epithelium in the lumen of glandular-like structures (arrows). H&E staining, scale bar 100 μm. (c–d) The marked Snail (c) and TGF-β2 (d) expression in gastric mucosa in rats of the experimental group is shown. Immunoperoxidase staining with antibody to Snail and TGF-β2, scale bar 100 μm. (e–f) Very weak Snail (arrows) (e) and TGF-β2 (f) expression in gastric mucosa in rats of the control group is shown. Immunoperoxidase staining with antibody to Snail and TGF-β2, scale bar 100 μm.
Figure 2. The pathological changes in stomach body. (a) Basal part of gastric glands with marked cytological and architectural atypia (arrows). In the box the selected area is shown. H&E staining, scale bar 200 μm (in box—100 μm). (b) Proliferations of atypical epithelium in the lumen of glandular-like structures (arrows). H&E staining, scale bar 100 μm. (c–d) The marked Snail (c) and TGF-β2 (d) expression in gastric mucosa in rats of the experimental group is shown. Immunoperoxidase staining with antibody to Snail and TGF-β2, scale bar 100 μm. (e–f) Very weak Snail (arrows) (e) and TGF-β2 (f) expression in gastric mucosa in rats of the control group is shown. Immunoperoxidase staining with antibody to Snail and TGF-β2, scale bar 100 μm.
Biomedicines 07 00021 g002aBiomedicines 07 00021 g002b
Biomedicines 07 00021 g003 550
Figure 3. The pathological changes in the pyloric stomach. (a) The dysplastic changes in the pyloric glands of stomach. H&E staining, scale bar 100 μm. In the box the polymorphic prismatic cells with large nuclei, having irregular hyperchromatism and irregular nucleoli in generative zone of pyloric glands are shown. H&E staining, scale bar 100 μm. (b) Positive reaction to Snail in cells lined the pyloric glands resembling signet ring cells. In the box the selected area with signet ring cells (arrows) is shown. Immunoperoxidase staining with antibody to Snail, scale bar 100 μm.
Figure 3. The pathological changes in the pyloric stomach. (a) The dysplastic changes in the pyloric glands of stomach. H&E staining, scale bar 100 μm. In the box the polymorphic prismatic cells with large nuclei, having irregular hyperchromatism and irregular nucleoli in generative zone of pyloric glands are shown. H&E staining, scale bar 100 μm. (b) Positive reaction to Snail in cells lined the pyloric glands resembling signet ring cells. In the box the selected area with signet ring cells (arrows) is shown. Immunoperoxidase staining with antibody to Snail, scale bar 100 μm.
Biomedicines 07 00021 g003
Biomedicines 07 00021 g004a 550Biomedicines 07 00021 g004b 550
Figure 4. Invasion of tumor cells. H&E staining. (a) Tumor embolus in the vessel, scale bar 100 μm. (b) Invasion of tumor cells in muscle layer (arrows), scale bar 100 μm. (c) Invasion of tumor cells in serosa layer (arrow). In the box the marked area is shown at magnification, scale bar 200 μm. (d) Invasion of tumor cells in omentum. In the box the selected area is shown at higher magnification, scale bar 200 μm. (e) The clusters of tumor cells in the muscle layer consisting of fibroblast-like cells with a curved shape (1-black arrows) and cells with finely dispersed oxyphilic inclusions in the cytoplasm (2-red arrows), scale bar 100 μm. (f) The cells with large, polymorphic, hyperchromic nuclei and with a markedly increased nuclear/cytoplasmic ratio in the muscle layer of stomach, scale bar 100 μm.
Figure 4. Invasion of tumor cells. H&E staining. (a) Tumor embolus in the vessel, scale bar 100 μm. (b) Invasion of tumor cells in muscle layer (arrows), scale bar 100 μm. (c) Invasion of tumor cells in serosa layer (arrow). In the box the marked area is shown at magnification, scale bar 200 μm. (d) Invasion of tumor cells in omentum. In the box the selected area is shown at higher magnification, scale bar 200 μm. (e) The clusters of tumor cells in the muscle layer consisting of fibroblast-like cells with a curved shape (1-black arrows) and cells with finely dispersed oxyphilic inclusions in the cytoplasm (2-red arrows), scale bar 100 μm. (f) The cells with large, polymorphic, hyperchromic nuclei and with a markedly increased nuclear/cytoplasmic ratio in the muscle layer of stomach, scale bar 100 μm.
Biomedicines 07 00021 g004aBiomedicines 07 00021 g004b
Biomedicines 07 00021 g005 550
Figure 5. Invasion of tumor cells in the muscle layer (a,c,d) and in omentum (b,d,f). Positive reaction to vimentin (a,b), Snail (c,d) and TGF-β2 (e,f). Immunoperoxidase staining with antibody to vimentin, Snail and TGF-β2, scale bar 100 μm.
Figure 5. Invasion of tumor cells in the muscle layer (a,c,d) and in omentum (b,d,f). Positive reaction to vimentin (a,b), Snail (c,d) and TGF-β2 (e,f). Immunoperoxidase staining with antibody to vimentin, Snail and TGF-β2, scale bar 100 μm.
Biomedicines 07 00021 g005
Biomedicines 07 00021 g006 550
Figure 6. Well-differentiated adenocarcinoma of cecum. H&E staining: (a) 200×, scale bar 200 μm, (b) 800×, scale bar 100 μm.
Figure 6. Well-differentiated adenocarcinoma of cecum. H&E staining: (a) 200×, scale bar 200 μm, (b) 800×, scale bar 100 μm.
Biomedicines 07 00021 g006
Biomedicines 07 00021 g007 550
Figure 7. Detection and characterization of calcium carbonate nanoparticles in the carcinogenic suspension and microcalcifications in the gastric mucosa. (a) Multiple microcalcifications in the gastric mucosa of experimental rats. von Kossa staining, scale bar 100 μm. (b) The absence of microcalcifications in the gastric mucosa of control rats. von Kossa staining, scale bar 100 μm. (c) The imaging of aggregates (nanoparticles) obtained by the atomic force microscopy. The scan size is 7.8 × 5.6 μm. (d) The histogram of calcium carbonate nanoparticles distribution in carcinogenic suspension according to their hydrodynamic radii, obtained by the dynamic light scattering method.
Figure 7. Detection and characterization of calcium carbonate nanoparticles in the carcinogenic suspension and microcalcifications in the gastric mucosa. (a) Multiple microcalcifications in the gastric mucosa of experimental rats. von Kossa staining, scale bar 100 μm. (b) The absence of microcalcifications in the gastric mucosa of control rats. von Kossa staining, scale bar 100 μm. (c) The imaging of aggregates (nanoparticles) obtained by the atomic force microscopy. The scan size is 7.8 × 5.6 μm. (d) The histogram of calcium carbonate nanoparticles distribution in carcinogenic suspension according to their hydrodynamic radii, obtained by the dynamic light scattering method.
Biomedicines 07 00021 g007

Share and Cite

MDPI and ACS Style

Senchukova, M.; Tomchuk, O.; Shurygina, E.; Letuta, S.; Alidzhanov, E.; Nikiyan, H.; Razdobreev, D. Calcium Carbonate Nanoparticles Can Activate the Epithelial–Mesenchymal Transition in an Experimental Gastric Cancer Model. Biomedicines 2019, 7, 21. https://doi.org/10.3390/biomedicines7010021

AMA Style

Senchukova M, Tomchuk O, Shurygina E, Letuta S, Alidzhanov E, Nikiyan H, Razdobreev D. Calcium Carbonate Nanoparticles Can Activate the Epithelial–Mesenchymal Transition in an Experimental Gastric Cancer Model. Biomedicines. 2019; 7(1):21. https://doi.org/10.3390/biomedicines7010021

Chicago/Turabian Style

Senchukova, Marina, Olesya Tomchuk, Elena Shurygina, Sergey Letuta, Eskender Alidzhanov, Hike Nikiyan, and Dmitry Razdobreev. 2019. "Calcium Carbonate Nanoparticles Can Activate the Epithelial–Mesenchymal Transition in an Experimental Gastric Cancer Model" Biomedicines 7, no. 1: 21. https://doi.org/10.3390/biomedicines7010021

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop