Search Results (1,917)

As primary producers in aquatic ecosystems, microalgae function not only as a natural source of nourishment for several economically important aquatic species but also as reservoirs of bioactive molecules. Microalgae can secrete exosome-like nanoparticles that transport functional biomolecules, such as proteins and nucleic acids, into the extracellular milieu, thereby mediating intercellular signaling and eliciting ecological or biomedical responses. Although plant-derived exosome-like nanoparticles have attracted attention for their utility in drug delivery and dermatology, the functional properties of microalgae-derived nanoparticles—particularly from species extensively applied in aquaculture—remain inadequately characterized. In this study, exosome-like nanovesicles were isolated from Nannochloropsis oculata (N-ELNs), a microalgal species widely used in aquaculture, and their skin-whitening potential was evaluated using the B16-F10 mouse melanoma cell model. The highest N-ELN yield was observed during the adaptation, exponential, and stationary growth phases. Uptake analyses confirmed the efficient internalization of N-ELNs by B16-F10 cells. Cell counting kit-8 assays indicated that N-ELNs exhibited no cytotoxic effects on melanoma cells or normal human dermal fibroblasts (HFF-1). Scratch wound healing assays revealed that N-ELNs exerted no significant effect on cellular migration. In B16-F10 cells, N-ELNs suppressed tyrosinase activity by downregulating Mitf and its downstream genes Tyr and Tyrp1, resulting in a substantial reduction in melanin synthesis (p < 0.05). The inhibitory effects of N-ELNs on melanin production, tyrosinase activity, and gene expression of Tyr, Tyrp1, and Mitf were comparable to those of the positive control, arbutin. Collectively, these findings suggest that N. oculata exhibits promising skin-whitening properties, providing a novel perspective for clinical applications and supporting the high-value utilization of the microalgae aquaculture industry. Full article

Journalists’ use of personal social media accounts and websites to disseminate content has necessitated investigating their significance for Kenyan media professionals. Based on a qualitative research design, this study draws on semi-structured in-depth interviews with Kenyan journalists (N = 22) to investigate their perceptions of migrating from traditional media outlets to digital platforms, in particular, personal social media channels and independent websites, the underlying reasons for this platform migration, and their perceptions of how legacy media are responding to such shifts. The findings highlight that economic incentives and challenging media environments are the primary drivers of platform migration and that participants perceive journalists’ independent websites (i.e., j-blogs) as valuable additions to the diversification of news sources. According to respondents, legacy media organizations have responded by restructuring their newsrooms, adopting convergence strategies, and establishing on-demand platforms to slow journalists’ migration to digital media. The implications for journalists, legacy and digital media, and media consumers are also discussed. Full article

Acute and chronic wounds are a major clinical burden, with persistent inflammation, impaired fibroblast function, defective angiogenesis, and disordered extracellular matrix deposition. The translational potential of existing in vitro models is limited by their poor durability and physiological relevance. The present paper aims to develop a robust in vitro organotypic model to simulate the early phases of both acute and chronic wounds and to validate it by testing the biocompatibility of clinically available wound dressings. Human fibroblasts and vascular endothelial cell lines were cultured at a ratio of 1:1 for 48 h, either on uncoated tissue culture plastic or on tissue culture plastic coated with a synthetic substrate (PhenoDrive-Y) that biomimics the extracellular matrix and promotes cell organization into tissue-like structures on a 2D plane (i.e., angiogenesis sprouting and fibroblast organization around it). Wound conditions were then created by damaging the formed structures using a conventional scratch procedure and introducing U937 human macrophage cells to the model to simulate either the onset of an acute wound or that of a chronic wound through the simultaneous spiking of the culture with relevant cytokines, i.e., IL-6 and TNF-α. The formation of new tissue-like structures in the scratch area was quantified by the extent of scratch closure after a further 24 h of incubation. Morphological analysis of wound healing was performed by light microscopy, while angiogenesis was assessed by CD31 immunostaining by confocal microscopy. The deposition of components of the extracellular matrix was determined both qualitatively and quantitatively by Picrosirius Red staining for collagen production and by Alcian Blue staining for glycosoaminoglycan synthesis on the adhering cells and their supernatants. Macrophage polarization into either M1 or M2 phenotype was studied by immunostaining with iNOS (M1) and CD206 (M2) antibodies by confocal microscopy. The model was validated by studying the gap closure areas in simulated acute and chronic wound-like conditions when incubated with clinically available wound dressings, N-A Ultra and Kaltostat. PhenoDrive-Y allowed the formation of tissue-like structures on the 2D tissue culture plane as opposed to the formation of cell monolayers on the uncoated tissue culture plastic. Upon mechanical damage, cell migration was significantly different; uncoated control co-cultures achieved complete closure as an indistinct monolayer by 24 h, while the organotypic wound models showed a slower percentage of damage closure. A further delay in the closure of the damaged area was observed when chronic wound-like conditions were simulated. Angiogenesis in chronic wound conditions was considerably impaired compared to the acute conditions. The analysis of the extracellular matrix component synthesis, specifically collagen and polysaccharides, revealed the deposition of dense, organized collagen fibers in the acute wound model, in contrast to the thin, fragmented collagen fibers and intracellular polysaccharides observed under chronic wound-like conditions. This corresponded to a statistically significant increase in the levels of both collagen and polysaccharides detected as soluble molecules in the supernatants. Macrophage polarization showed no statistically significant differences in the acute and chronic wound models, though iNOS did significantly decrease after N-A application in acute and chronic models. However, acute wound-like conditions showed a restoration of the vascularized tissue-like structures after treatment with these types of dressings, albeit through different organizational pathways, whereas only minimal improvement was noted under chronic wound conditions, particularly in the case of the N-A dressing. The organotypic dermis model for the onsets of acute and chronic wounds emerges as a highly versatile tool to understand healing mechanisms in the absence or presence of co-morbidities and to assess the biocompatibility of wound dressings as well as the safety, efficacy and dosage of drugs. Full article

Background: Obesity is a recognized risk factor for developing breast cancer (BC), but factors involved remain unclear. We investigated if breast adipose tissue from healthy women, BRCA1/2 mutation carriers and BC patients, can stimulate BC cell line migration and activation. Methods: adipose tissue conditioned medium (ATCM), was prepared from breast adipose tissue from healthy subjects (naïve; group 1 (n = 20)), BRCA1/2 mutation carriers (group 2 (n = 22)) and BC patients (group 3 (n = 38)). ATCM effect on migration of BC cell lines MCF-7, SK-BR-3 and MDA-MB-231 was measured with xCELLigence (ACEA Biosciences, San Diego, CA, USA) cell migration assay. Activation of migration was determined by measuring filopodia activation. Migration and filopodia activation were related to body mass index (BMI) and BC subtypes. Luminex multiplex assay was performed to examine the secretory profile of adipose tissue. Results: ATCM from group 1 induced migration and filopodia activation in MCF-7 and MDA-MB-231, but not in SK-BR-3. ATCM from group 2 induced filopodia activation but no migration. ATCM from group 3 induced less migration in MCF-7 than ATCM from group 1. Higher BMI was associated with increased ATCM-induced activation in MCF-7 (group 1) and MDA-MB-231 (group 2). ATCM from group 1 and 2 showed a metabolic secretory profile, whereas group 3 showed higher pro-angiogenic and inflammatory cytokines. Conclusions: This study shows that breast adipose tissue from healthy women, BRCA1/2 mutation carriers and BC patients, can stimulate BC cell line migration and activation. This effect is related to BC subtype and BMI. These data improve insight in adipose tissue as factor in BC development. Full article

Melanoma is an aggressive cancer characterized by a rapid metastatic process. Thus, understanding the mechanisms underlying its progression is urgently needed to improve patient outcomes. In this regard, there is consistent evidence of a tumor-sustaining crosstalk between melanoma and subcutaneous adipose tissue; however, the role of extracellular vesicles (EVs) in this communication still needs to be clarified. We demonstrated that the EVs derived from adipocytes did not alter melanoma cell proliferation but significantly promoted tumor cell migration and invasion by determining an enrichment in mesenchymal markers, such as N-cadherin and vimentin. In particular, these changes were accompanied by the transition towards a stem-like phenotype, characterized by enhanced spherogenic ability and ABCG2 upregulation; interestingly, this led to a reduced in vitro response to the BRAF inhibitor vemurafenib. Mechanistically, an increase in PGC-1α expression was found, resulting in higher mitochondrial mass and activity, ATP synthesis, and ROS overproduction; of note, treatment of melanoma cells with SR-18292 and XCT790, two inactivators of mitochondrial biogenesis, and N-acetylcysteine, a ROS scavenger, successfully counteracted the above EV-related effects, suggesting that mitochondrial function could be targeted to suppress the vesicular interactions between adipose tissue and melanoma. Taken together, these results highlight the crucial role played by EVs in melanoma stroma, pointing out the ability of adipocyte-derived vesicles to sustain cancer aggressiveness via PGC-1α–dependent mitochondrial reprogramming. Full article

Cortex Lycii Radicis, a medicinal plant, has been reported to inhibit epithelial–mesenchymal transition (EMT) and exhibit anti-lung cancer properties. Our previous study identified its major compound, Kukoamine B (KuB), as an inhibitor of membrane PD-1/PD-L1 interaction, thereby restoring T-cell function. However, the effect of KuB on EMT and the underlying mechanism thereof remain unknown. Herein, we show that PD-L1 overexpression enhances the proliferation, migration, and EMT of LUAD cells, upregulating N-cadherin and Vimentin, while downregulating E-cadherin. Mechanistically, PD-L1 directly binds phosphorylated p65 (p-p65) and facilitates p65 nuclear translocation, an interaction confirmed by molecular simulations. We found that KuB disrupts the PD-L1/p65 complex, impedes p65 nuclear translocation, and suppresses EMT, proliferation, and migration in LUAD cells. These inhibitory effects were reversed by PD-L1 overexpression. We therefore conclude that KuB suppresses EMT in LUAD by targeting intracellular PD-L1, blocking PD-L1–p65 interaction and nuclear translocation of p65. Full article

Prostate cancer (PCa) is the most general cancer in men and is often linked with distant metastasis in its later stages. The caffeic acid (CA) derivative, N-(4-methoxyphenyl)methylcaffeamide (MPMCA), demonstrates superior liver-protective effects compared to CA. Nevertheless, the functions of MPMCA on prostate cancer metastasis remain unclear. Here, we demonstrate that MPMCA blocks migration and invasion in prostate cancer cells without affecting cell viability. By suppressing the production of mesenchymal markers Vimentin, N-cadherin and β-catenin and upregulating the production of the epithelial marker Zonula Occludens-1 (ZO-1), MPMCA also controls Epithelial–Mesenchymal Transition (EMT). The Phosphoinositide 3-kinase (PI3K), Protein kinase B (AKT) and mechanistic target of rapamycin (mTOR) pathway has been documented to regulate MPMCA-inhibited cell motility. Transfection with Snail and Slug cDNA reverses MPMCA’s suppression of EMT, migration, and invasion in prostate cancer cells. Importantly, our in vivo data indicates that MPMCA reduces Snail and Slug expression and prostate cancer metastasis. Our evidence suggests that MPMCA is a novel therapeutic candidate for treating metastatic prostate cancer. Full article

Heavily doped metal oxide thin films combining high visible transmittance and low electrical resistance are used in a multitude of optoelectronic devices, where their performance is highly dependent on the structural defects and density of electronic states associated with doping. This study explores the structural, optical, and electronic properties of Sn-doped indium oxide (In₂O₃:Sn) and Al-doped zinc oxide (ZnO:Al) thin films, which were prepared by sputtering on unheated glass substrates and subsequently annealed in N₂ at different temperatures between 250 °C and 450 °C. These samples reach free electron densities above 10²⁰ cm⁻³ due to the presence of extrinsic donors (mainly substitutional defects of Sn_In and Al_Zn) and also intrinsic donors (oxygen vacancies), which change with the annealing temperature due to oxygen desorption and/or cation migration processes. The volume of the crystal lattice expands (up to a maximum of 1.1%) and the band gap widens (up to a maximum of 17.9%) with respect to the undoped material, increasing with electron density. Additional absorption is due to band tail, at an energy ~10% below the undoped band gap, which varies slightly with the carrier concentration. The same general behavior is observed for both materials, with particularities in terms of crystal lattice and electronic states, which can be tuned by the heating temperature. Full article

To advance automatic tomato leaf disease detection in precision agriculture, this study addresses critical challenges in complex field environments, such as variable lesion scales, background interference, and deployment constraints. We propose MSP-Net, a task-driven detection framework with targeted architectural refinements integrating three specific optimizations. First, a Multi-Scale Perception Convolution Module (MSPCM) is introduced to capture diverse disease features across early-to-late infection stages. Second, SimAM-enhanced C3k2 layers are utilized to suppress background noise and focus on fine-grained lesion cues. Third, a Multi-Scale Feature Enhancement Module (MSFEM) bridges the semantic gap between shallow and deep features to improve fusion efficacy. Furthermore, we construct a lightweight variant, L-MSP-Net, using architectural migration and structured pruning for edge efficiency. Experimental results on the real-world Tomato-Village dataset show that MSP-Net achieves 92.0% mAP@0.5, outperforming the YOLOv11s baseline by 2.0%. L-MSP-Net attains 86.1% mAP@0.5, improving by 3.6% over the lightweight YOLOv11n baseline while reducing parameters by 10.5%, and is successfully deployed on the RK3588 edge platform. Additional cross-dataset experiments on PASCAL VOC and MS COCO evaluate the transferability of the proposed architectural refinements to generic object detection tasks. Full article

The Integrated Fixed-film Activated Sludge (IFAS) partial nitritation/anammox (PN/A) process offers robust nitrogen removal, yet startup using pre-colonized carriers incurs high logistical costs. This study investigated the mechanism of inoculating a pilot-scale IFAS system with granular anammox sludge to treat anaerobic digestion supernatant. The treatment train integrated coagulation, pre-aeration, and an IFAS-PN/A unit. The granular-inoculated IFAS-PN/A unit achieved stable biofilm formation and a nitrogen removal rate of 0.36 kg N m⁻³ d⁻¹, benefiting from the effective interception of excessive organic carbon by the preceding coagulation and pre-aeration steps. Microbial analysis identified Candidatus brocadia as the dominant anammox genus, revealing a distinct migration pathway: bacteria transferred from disintegrating granules to the suspended sludge—acting as a transitional vector—before ultimately colonizing the carriers. While granular biomass diminished, anammox abundance in the biofilm increased to 12.0% by day 166. Furthermore, distinct spatial niches were observed: ammonium-oxidizing bacteria (AOB) dominated the suspended sludge, while nitrite-oxidizing bacteria (NOB) were effectively suppressed. These findings demonstrate the feasibility of granular inoculation for cost-effective IFAS startup and provide critical insights into the bacterial migration dynamics required for stable operation. Full article

In this study, the diffusion barrier performance of TiN and SiC layers was investigated in Si/TiN/Cu, Si/TiN/SiC/Cu, and Si/SiC/TiN/Cu multilayer structures to address copper diffusion issues at silicon interfaces in microelectronics. Samples were annealed in argon at 500–800 °C for 30 min, and diffusion behavior was analyzed using X-ray diffraction (XRD) and sheet resistance measurements. The Cu₃Si phase formed at 600 °C in the Si/TiN/Cu system, while no Cu₃Si appeared in the Si/SiC/TiN/Cu system up to 700 °C, indicating improved stability. Complete copper diffusion occurred in all systems at 800 °C. Sheet resistance measurements corroborated the XRD findings, demonstrating that multilayer structures incorporating TiN and SiC significantly enhance thermal stability and suppress copper diffusion. Comparison of Si/SiC/TiN/Cu and Si/TiN/SiC/Cu stacks annealed at 700 °C revealed that the stability of TiN depends on layer sequence, with SiC effectively blocking Cu migration into TiN when placed adjacent to Cu. Structural and morphological properties of TiN films were also examined, confirming their suitability as diffusion barriers. Additionally, the feasibility of forming a low-resistivity TiSi₂ layer through a single annealing step to create a TiSi₂/TiN system was explored, highlighting potential applications in advanced device integration. Full article

Introduction: Follicular lymphoma (FL) is the most common indolent non-Hodgkin lymphoma. Approximately 20% of patients experience early relapse within 24 months (POD24) of immunochemotherapy (ICT), a subgroup associated with poor prognosis and not well-identified by current prognostic indices. Given that tumor mutational burden (TMB) has been associated with outcome in various cancers, we investigated its potential as a prognostic biomarker in FL. Methods: TMB was estimated by next-generation sequencing using a 409-gene panel in a cohort of 119 patients diagnosed with FL grades 1–3A and treated with frontline immunotherapy or ICT. Results: Although TMB was not associated with clinical variables in non-transformed FL patients, higher TMB values were observed in patients harboring the t(14;18) translocation, mutations in BCL2, TNFRSF14, or genes involved in cellular migration (GNA13, GNAI2). Notably, patients with high TMB (>2.55 mutations per megabase) showed longer progression-free survival, lymphoma-specific survival, and overall survival, and had fewer mutations affecting the mTORC1 pathway. A higher proportion of POD24 patients was observed in the low TMB subgroup. In 25 paired diagnosis-relapse samples, TMB remained globally stable, although variations in the molecular landscape were observed. In addition, we analyzed TMB in a separate cohort of patients presenting transformed FL at diagnosis (n = 16). Higher TMB was also associated with the t(14;18) chromosomal translocation, but not with clinical features or survival. Conclusions: These findings support the potential of TMB as a prognostic biomarker in FL, providing molecular understanding beyond established clinical indices and aiding in the identification of patients at higher risk of early progression following ICT. Full article

The Sinian (Ediacaran) Dengying Formation in the northeastern Sichuan Basin exhibits a significant exploration potential. Nevertheless, the great burial depth of carbonates in the Dengying Formation and the scarcity of drilling data have imposed constraints on in-depth investigations into the evolution of lithofacies paleogeography as well as the primary controlling mechanisms. Through integrated analysis of field outcrops, core and well logging data, the evolution of the lithofacies and paleogeography of the Dengying Formation in the northeastern Sichuan Basin was reconstructed by using 3D stratigraphic forward modeling. The study area is predominantly characterized by platform margin facies and restricted platform facies, comprising four subfacies including microbial (algal) mound, grain shoal, intershoal sea, and intraplatform depression. The microbial (algal) mound and grain shoal subfacies are primarily developed along the western and eastern platform margins, exhibiting a near north–south trend. Scattered mound–shoal complexes and intershoal sea occur within the platform, with localized intraplatform depression zone. During the depositional stage of the Dengying Formation, three primary paleogeomorphic units were developed including the platform margin topographic high zone, intraplatform gentle slope zone, and intraplatform depression zone. During the Deng-1 and Deng-3 periods, sea level rise increased accommodation space, leading to a gradual decline in carbonate productivity and limited development of the mound–shoal complexes. In contrast, during the Deng-2 and Deng-4 periods, sea level decreased, water depth decreased, and carbonate productivity was enhanced, resulting in extensive development of the mound–shoal complexes. The simulation results indicate that carbonate-producing ecosystems thrive when wind blows from 270° W (80% frequency) or 15° N (60% frequency); with an effective water depth of 10–20 m, the elevated carbonate productivity is conducive to the growth of biogenic calcification. Comprehensive analysis suggests that paleogeomorphology, eustatic fluctuations, and paleowind fields collectively control the distribution and evolution of the lithofacies in the Dengying Formation in the northeastern Sichuan Basin. Paleogeomorphology governs the types and distribution of sedimentary facies belts as well as the spatial arrangement of lithofacies. Eustasy determines the magnitude of mound–shoals and their lateral migration. Three-dimensional stratigraphic forward modeling offers a novel approach for reconstructing paleogeographic evolution of carbonate platforms and analyzing key controlling factors, while also enhancing our ability to predict the distribution patterns of mound–shoal complexes. Full article

Background: β-thalassemia is a rare genetic disorder affecting 1–5% of the global population and poses a health burden due to migration of individuals from endemic regions. Identifying asymptomatic β-thalassemia carriers is essential to prevent the birth of thalassemic babies. A simple, sensitive method compatible with self-sampling could enhance the detection of β-thalassemia in the population. Methods: Capillary blood was collected via dried blood spot (DBS) and dried blood matrix (DBM) from 18 members (52.9%, 18/34) of a three-generation family. Hemoglobin was extracted, and globin chains were analyzed on a triple quadrupole mass spectrometer (TQMS). δ/β (%) was utilized as a biomarker to identify β-thalassemia. Venous blood collected from positive and negative individuals (n = 11) was further tested to confirm the findings and validated with complete blood count (CBC) and Capillary Electrophoresis (CE). Results: β-thalassemia was detected in seven individuals: three from generation I, three from generation II, and one from generation III. CBC showed thalassemia indices, while CE demonstrated elevated HbA2 consistent with β-thalassemia. Molecular sequencing of two samples confirmed the heterozygous c.92 + 5 G > C mutation in the β-globin gene. The overall prevalence of β-thalassemia in the family was 20.6% (7/34). High clinical performance was achieved across sample types, with 100% sensitivity for DBS, 100% specificity for DBM, and an overall accuracy of 91% when compared with CE. Conclusions: TQMS in combination with CBC parameters successfully identified asymptomatic heterozygous β-thalassemia carriers using self-sampling techniques. Cascade screening within affected families emerges as a possible strategy for early detection of β-thalassemia pending comprehensive validation. Full article

Parkia speciosa (P. speciosa), a plant utilized in traditional medicine, has shown promise in various therapeutic applications and contains multiple bioactive components (saponins, alkaloids, flavonoids, polyphenols, and terpenoids). These bioactive compounds have attracted increasing scientific interest due to their ability to modulate key cancer-associated pathways, including the inhibition of cell proliferation and migration and the suppression of oxidative stress and inflammation mechanisms. However, despite P. speciosa’s historically long and wide-ranging usage, a comprehensive investigation of these properties has not been conducted for its pod. This study investigated the effects of P. speciosa empty pod extract (PSET) on human colorectal cancer cells. The extract demonstrated significant dose-dependent inhibition of colorectal cell migration, invasion, and colony formation while exhibiting no cytotoxicity toward normal colon epithelial cells. Western blot analysis confirmed reduced expression of Matrix metalloproteinases 2 (MMP2), Matrix metalloproteinases 9 (MMP9), and N-cadherin, indicating suppression of the epithelial–mesenchymal transition (EMT). These findings demonstrate that the PSET effectively inhibits metastasis in colorectal cancer cells through the EMT pathway, suggesting its potential as a dietary supplement or therapeutic agent for colorectal cancer treatment. Our research provides support for the development of natural, less toxic alternative cancer treatments. Therefore, PSET shows potential for development as a dietary supplement or therapeutic agent for the treatment of colon cancer. Full article