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Article

Novel 2-Amino-1,4-Naphthoquinone Derivatives Induce A549 Cell Death through Autophagy

by
Hua-Yuan Tan
1,†,
Feng-Ming Liang
1,†,
Wen-Jing Zhang
1,
Yi Zhang
1,
Jun-Hao Cui
1,
Yu-Yu Dai
1,
Xue-Mei Qiu
1,
Wen-Hang Wang
1,
Yue Zhou
1,2,
Dan-Ping Chen
1,2,* and
Cheng-Peng Li
1,2,*
1
School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China
2
Guizhou Engineering Laboratory for Synthetic Drugs, Guizhou University, Guiyang 550025, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2023, 28(8), 3289; https://doi.org/10.3390/molecules28083289
Submission received: 6 February 2023 / Revised: 14 March 2023 / Accepted: 28 March 2023 / Published: 7 April 2023
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Abstract

:
A series of 1,4-naphthoquinone derivatives containing were synthesized as anti-cancer agents and the crystal structure of compound 5a was confirmed by X-ray diffraction. In addition, the inhibitory activities against four cancer cell lines (HepG2, A549, K562, and PC-3) were tested, respectively, and compound 5i showed significant cytotoxicity on the A549 cell line with the IC50 of 6.15 μM. Surprisingly, in the following preliminary biological experiments, we found that compound 5i induced autophagy by promoting the recycling of EGFR and signal transduction in the A549 cell, resulting in the activation of the EGFR signal pathway. The potential binding pattern between compound 5i and EGFR tyrosine kinase (PDB ID: 1M17) was also identified by molecular docking. Our research paves the way for further studies and the development of novel and powerful anti-cancer drugs.

Graphical Abstract

1. Introduction

Cancer is the second most common serious public health problem behind cardiovascular diseases [1]. The burden of the incidence rates and mortality of cancers is rapidly increasing worldwide [2]. For this reason, the discovery of new and effective anti-cancer drugs for malignant tumor treatment is an urgent task, and at the same time, the development of promising anti-cancer agents becomes one of the research hotspots that attracts the great attention of chemists and pharmaceutical scientists. Death patterns of tumor cell are regulated by multiple signaling pathways. Autophagy is a physiological cellular process that degrades and eliminates misfolded proteins and damaged organelles, which plays a vital role in adaptive starvation, development, cell death, and tumor inhibition [3,4]. The development of new drugs and the study of the mechanism that causes tumor cells’ death is a feasible approach for advances in cancer therapy.
The NCI (National Cancer Institute) demonstrated that quinone derivatives were a class of important active structures that are capable of inhibiting the proliferation of cancer cells. Among all the quinone structure compounds, naphthoquinone exhibits a more remarkable biological activity than the others, especially in terms of its anti-tumor activity. The 1,4-naphthoquinone structure, known as a kind of ubiquitous natural compounds [5,6,7,8], is a typical structure for the development of perspective drugs, which is usually separated and purified from natural plants (such as xanthium sibiricum [9]). Except for being used as the raw material for the synthesis of medicine and pesticides [10], 1,4-naphthoquinones also display a wide range of biological activities [11,12], such as anti-bacterial [13,14,15,16,17,18,19], anti-virus [20,21,22,23,24], anti-cancer [25,26,27], anti-malaria [28], treatment of protozoal disease [29], anti-Alzheimer’s disease [30], inhibition of atherosclerosis, elimination of free radicals [31], inhibition of platelet activity [32], trypanocidal [33], and anti-inflammatory [34]. So the structure of 1,4-naphthoquinone has amazing potential for different kinds of medical applications. Recently, various anti-cancer drugs containing 1,4-naphthoquinone structural units [35], such as doxorubicin, daunorubicin, atovaquone [36], buparvaquone [37], shikonin, etc. (Figure 1), were used for solid tumors therapy, including lung cancer, prostate cancer, and breast cancer, which achieved great therapeutic effects. In brief, 1,4-naphthoquinone derivatives are able to provide a new insight for the development of new anti-cancer drugs through the further modification of the potential leading compounds to enhance their biological activities [38].
Based on the remarkable biological activity of 1,4-naphthoquinone derivatives in inhibiting the growth of tumor cells, recently, an increasing number of pharmacists devoted themselves to the continuous innovation and design of promising 1,4-naphthoquinone structure drugs, the comprehensive study of the relationship between compound structures and biological activities, and the investigation of the mechanism concerning the inhibition of the growth of tumor cells. The previous research found that 1,4-naphthoquinone derivatives containing an amide structure enabled the improvement of anti-tumor activities significantly [39,40]. The amide group is regarded as a common active structural segment based on its anti-bacterial [41], insecticidal [42], anti-cancer [43] and other biological activities, which is often introduced to design drugs that are expecting to achieve great therapeutic effect. The introduction of an amide structure is able to increase the polarity and solubility of anti-tumor drugs. More importantly, the pharmacological effects of amino anti-tumor drugs are greatly improved based on the interaction between target proteins and molecules [44,45,46,47,48,49,50,51].
Inspired by the high activity of 1,4-naphthoquinone derivatives and the interaction ability of an amide structure, we designed and synthesized a series of two amino-substituted 1,4-naphthoquinone derivatives based on the principle of drug splicing, expecting to obtain promising anti-tumor agents. The crystal structure of the target compound 5a was confirmed through X-ray diffraction, and the inhibitory activities of the synthesized compounds on A549 (non-small human lung cancer), PC-3 (prostate cancer l), K562 (chronic myeloid leukemia), and HepG2 (liver cancer) were studied by the MTT method, and compound 5i was found to exhibit a high anti-proliferative activity against A549 cancer cells in vitro. Subsequently, 5i was further investigated to analyze its anti-tumor mechanism of A549 cancer cells.

2. Results

2.1. Chemistry

In order to obtain the target compounds 5a–5u with different substitutions and 9a–9g containing the amide group, we designed a simple and feasible synthesis route, and the synthesis route in this work is shown in Figure 2. In the first synthesis route, intermediate 3 was prepared by the reaction of different substituted aniline with bromo-acetyl bromide, which was followed by a reaction with 2-hydroxy-1,4-naphthoquinone to synthesize the compounds 5a–5u in a DMF solvent. The yield of the compounds 5a–5u was 42.33–81.65% by the 1:1 ratio of cesium carbonate to 2-hydroxy-1,4-naphthoquinone. Secondly, compounds 9a–9g that contained an amide structure were synthesized by 1,4-naphthoquinone and 3-amino-p-methylene acid, and copper acetate worked as the catalyst to obtain intermediate 8 [52]. Compounds 9a–9g were prepared by reactions of intermediate 8 with different substituted aliphatic amines or anilines under alkaline conditions of the DIPEA (N,N-Diisopropylethylamine) and HATU (2-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate) mixture with yields of 43.24–60.64%. All the unreported synthesized compounds were confirmed by 1H NMR, 13C NMR, and HRMS spectrums, and the characterized materials are displayed in the supporting information.

2.2. Crystal Structure Determination

In order to verify the feasibility of the synthetic route of the new compounds 5a–5u, a single crystal of compound 5a was cultured after the purification based on the gas phase diffusion method, and the crystal structure was obtained and identified by an X-ray single-crystal diffraction. The process was as follows: nearly 10–20 mg 5a was dissolved in a DMSO, filtered through a 0.22 μm membrane, injected into a small culture bottle, sealed with a sealing membrane that left a gap of 4–5 pinholes, and finally, put into a large culture bottle with an appropriate amount of a low boiling solvent (water) at the bottom. What was noteworthy was that the sealed samples were placed at the indoor ambient temperature (about 25 °C) for fixation to enable the system to diffuse slowly.
The single-crystal structure of compound 5a was analyzed by Olex-2 software, and the results are shown in Figure 3. Compound 5a was the colorless single crystal. The crystal data of C17H13NO2 (M = 263.290 g/mol) were as follows: orthorhoombic, space group P212121 (no. 19), a = 7.3985(3) Å, b = 12.1825(4) Å, c = 15.1213(5) Å, V = 1362.92(8) Å3, Z = 4, T = 273.15 K, μ(Cu Kα) = 0.680 mm−1, Dcalc = 1.278 g/cm3, 7003 reflections measured (9.32° ≤ 2Θ ≤ 33.14°), and 2353 unique (Rint = 0.0514, Rsigma = 0.0512), which were used in all the calculations. The final R1 was 0.0526 (I ≥ 2u(I)) and wR2 was 0.1819.

2.3. Biological Activity

In this work, gefitinib (G) and 5-fluorouracil were used as the positive controls, and the in vitro cytotoxic activities of all the synthetic compounds against the A549, PC-3, K562, and HepG2 cell lines were evaluates in an MTT assay. The cytotoxic activities’ results of compounds 5a–5u after 48 hours of treatment are shown in Table S1 (Supplementary Materials), and most of the target compounds exhibited a good inhibitory activity against the A549, PC-3, HepG2, and K562 cancer cells. The anti-proliferative activity data of the compounds 9a–9g are listed in Table S2 (Supplementary Materials), and the results suggest that the propylamine-, butylamine-, and 3-fluorophenyl-substituted compounds displayed high bioactivities.
Based on the significant bioactivity of most of the target compounds against the A549 cells, we further selectively evaluated the anti-proliferative activity of these 1,4-naphthoquinone derivatives against cell carcinoma lines, and the results are summarized in Table 1. Most of the synthesized compounds showed IC50 (50% of the compounds that inhibit cancer cell growth) values below 20 µM. Moreover, the IC50 values of compounds 5a, 5b, 5i, 5l, 5m, 5p, and 5t were below 10 µM, indicating the remarkable anti-tumor ability of these compounds. An interesting phenomenon was found in compounds 5a-5u once they shared the same substituent groups R, and their activities were different at various substitution positions, such as compound 5d (R = 2-Cl, 20.32 µM) > 5e (R = 3-Cl, 23.45 µM) > 5f (R = 4-Cl, 50 µM). According to the bioactivity data, we supposed that the design substituent at two or three sites of the target compounds enabled better anti-tumor activity than four of the site substituent. For the results of compounds 9a–9g, an increase in the length of the chain–alkane substituent groups appropriately facilitated an improvement in activity, such as for compound 9b (R = propylamine, 22.0 µM) > 9a (R = butylamine, 20.32 µM). The IC50 values of the halogen-substituted compounds 9d–9g were lower than that of compound 9c when the substituted group was the benzene ring. Above all, compound 5i exhibited the best anti-tumor activity against A549 with an IC50 value of 6.15 µM, indicating that the 3-F substituent facilitated the enhancement of anti-tumor activity. Hence, 5i was selected as the candidate compound for further pharmacological study to explore its anticancer mechanisms.

2.4. Interaction of EGFR with Compound 5i

The binding mode between the EGFR (Epidermal Growth Factor Receptor) (PDB: 1M17) and compound 5i is shown in Figure 4A,B. The simulation results indicated that 5i exhibited its binding ability by penetrating into the binding bag of the EGFR. In the binding bag, the oxygen atom in the naphthoquinone ring could form hydrogen bonds with the nitrogen atom of Asp (aspartic acid) 831 in the EGFR and the hydrogen bond of the oxygen atom of Thr (threonine) 830 in the EGFR, respectively (Figure 4C,D). In addition, the benzene ring on the naphthoquinone of compound 5i was able to interact with the carbon atom of Lys (lysine) 721 to form pi-H (Figure 4C,D). These interactions between EGFR and 5i mainly changed the binding energy and had impacts on the EGFR-associated pathway in vivo.

2.5. Compound 5i Induced ROS Accumulation in A549 Cell

Naphthoquinone derivatives were reported that induced the intracellular ROS (reactive oxygen species) accumulation to affect the therapeutic effect [53]. To investigate the potential relationship between compound 5i and ROS production, we treated A549 cells with 5i at different concentrations for 6 h and 12 h, and observed the changes of ROS by flow cytometry. At the earlier stage (6 h), poor ROS accumulation was observed both in 5i-treated and control groups. This result might indicate that compound 5i had not yet had enough time to induce large numbers of ROS production. When the incubation time was 12 h, the ROS level in A549 cells significantly increased compared to the negative controls, which was nearly a three-fold increase (Figure 5A,B). As shown by the high levels of ROS, we speculated that compound 5i inhibited the proliferation of cancer cells by inducing ROS accumulation.

2.6. Effect of 5i on EGFR Signal Pathway-Related Proteins

To further investigate the inhibitory mechanism of compound 5i on A549 cells, firstly, we studied the impact of 5i on the EGFR-associated signal pathway through detecting the expression of EGFR, AKT, and their phosphorylated proteins at 10 and 20 μM, respectively, by the Western blot assay. As shown in Figure 6A,B, we found that the proteins expression was obviously different between the 5i treatment group and the blank control group. Compound 5i significantly up-regulated the expressions of p-Akt, which were translated by tumor suppress genes, and the levels of p-EGFR and Akt remained unchanged regardless of treatment with 5i or gefitinib at 10 μM. Interestingly, EGFR protein expression was down-regulated remarkably after treatment with 5i (10 μM), which lower three times lower than the control group. However, little fluctuation of the EGFR was observed after treating with 10 μM gefitinib, which indicates that compound 5i playa a distinctive role in the regulation of the EGFR pathway to affect A549 cells. Hence, combined with the above results, we preliminarily suspect that compound 5i will induce autophagy by promoting EGFR recycling and signal transduction in A549 cells to activate the EGFR signaling pathway.

2.7. The Effect of Compound 5i on the Expressions of the Autophagy-Related Protein LC3

Autophagy has been found to play a key role in physiological and pathological processes in vivo, and the appropriate modification of autophagy could accelerate the apoptosis process of tumor cells and enhance the efficacy of chemotherapy [54,55,56]. It has been known that LC3 proteins are associated with autophagy in vivo [57,58]. To verify whether compound 5i could affect the autophagy process in A549 cells, this work studied the expression of the autophagy-related protein LC3 in Western blotting experiments. After treatment with 5i for 48 h, we found that LC3-I down-regulated significantly, and on the contrary, LC3-II was up-regulated twice at 10 and 20 μM compared control group (Figure 7A,B). However, the positive drug gefitinib seemed to have little influence on the expression of LC3-II in the A549 cells. Remarkable changes between LC3-I and LC3-II after treatment with 5i indicated that 5i might play a vital role in inducing the death of A549 cells through autophagy to achieve a good anti-tumor effect.

3. Discussion

Autophagy is an important metabolic regulation mechanism, which can remove dysfunctional organelles and extra macromolecules to protect cells against damage from various stress reactions [59,60]. An increasing number of evidence has shown that autophagy plays a critical role in diverse human physiological and pathological processes, including tumors and infections [61]. A great variety of investigations demonstrated that tumor cells with defects in the autophagy facilitated a malignant transformation [62], indicating that autophagy might be a potential anti-tumor target, which was worthy of further study and exploration to develop promising drug molecules. In recent years, small chemical molecules became an important tool for treating cancers and exploring the basic biological mechanisms and processes of malignant tumors [63,64,65,66,67,68,69].
Overall, naphthoquinone derivatives have shown anti-cancer effects against various cancers through a variety of mechanisms. Most reported strategies for the development of anti-tumor drugs were focused on DNA damage through ROS production, the inhibition of topoisomerase II, the inhibition of tumor suppressor p53, and the induction of apoptosis through ERS. In this study, we synthesized a series of new 1,4-naphthoquinone derivatives containing two amino substituents, and screened a promising compound 5i by in vitro biological activity testing, followed by an investigation of its anti-cancer mechanisms. We found that the inhibitory activity of 5i on the growth of A549 cells might have resulted from autophagy, based on the regulation of LC3 proteins expression that was associated with autophagy. Our research results indicated that autophagy could be a potential anti-tumor target of the two amino-substituted 1,4-naphthoquinone derivatives. In this work, an interesting experimental phenomenon that was different from the widely reported mechanism of naphthoquinone derivatives was found and analyzed.
It is worth mentioning that doxorubicin (ADR), a class of anthracycline antibiotics, is a highly effective, broad-spectrum, anti-tumor antibiotic that is widely used in the clinical treatment of breast cancer, lung cancer, lymphoma, and other malignant tumors. However, ADR is limited to cardiomyopathy treatment based on its toxicity, which results in congestive heart failure and death. Various speculations on the ARD induction of cardiotoxicity were proposed, and the oxygen-free radical theory was accepted. ARD is supposed to be involved in the key cellular REDOX process that produces large numbers of ROS, which leads to the modification and degradation of nucleic acids and proteins in cells. To avoid these side effects, ARD is usually enclosed in drug carrier, taking the liposomes as an example, which deliveries ARD to the desired organs and alters the pharmacological distribution of the drug to avoid damage of the heart by an excess of ARD. In addition, it has also been reported that ARD-liposome enabled the preferential accumulation of drugs in target tumors, so that the performance of ARD was enhanced dramatically [70].
Similarly, quinone derivatives are widely used as anti-oxidants or mediators ascribed to the formation of ROS with superoxide anion radicals, hydrogen peroxide, hydroxyl radicals, and singlet oxygen [71]. Based on the redox characteristic of naphthoquinone derivatives, in this study, we studied the generation of ROS in A549 cells that were induced by compound 5i via flow cytometry, and we found that the ROS levels increased significantly after 12 h of co-incubating with compound 5i. In future studies, compound 5i should be enclosed in liposomes or modified by specific peptides to avoid the potential side effects and targets to the diseased organs.

4. Materials and Methods

4.1. Chemistry and Instruments

All the starting materials, reagents, and solvents for synthesis of target compounds are commercially available unless otherwise specified. All the reactions were monitored by thin layer chromatography (TLC) on a silica gel plate (GF254) and observed under ultraviolet light (254 and 365 nm). All solvents and reagents were reagent-grade without further purification. NMR data were obtained by Bruker Ascend 400 and 500 MHz (Bruker Optics, Switzerland). The following abbreviations are used to describe peak-splitting modes: s (singlet), d (two-state), t (tristate), m (polymorphic), and dd (two-state of two-state). The coupling constant is expressed in Hertz units (Hz). For the single-crystal data of compound 5a, the X-ray diffraction data of single crystal were recorded by Bruker D8 QUEST diffractometer and analyzed by Olex-2 software. High resolution mass spectrometry (HRMS) spectra were conducted using a Thermo Scientific Q Exactive (Thermo Scientific, St. Louis, MO, USA). The melting points (m. p.) for all title 1,4-naphthoquinone derivatives were detected using a (X-4D) digital micro melting point apparatus.

4.2. Pharmacology

4.2.1. Cell Culture and Treatment

Non-small human lung cancer (A549), chronic myeloid leukemia (K562), prostate (PC3), and liver (HepG2) cells were purchased from the Cell Bank of the Chinese Academy of Sciences (Kunming, China). A549, K562, and PC3 cells were cultured in RPMI-1640 medium and HepG2 were cultured in MEM medium. All mediums were supplemented with 10% fetal bovine serum (FBS), 100 μg/mL penicillin, and 100 μg/mL streptomycin. All cells were cultivated in 5% CO2 incubator at 37 °C.

4.2.2. MTT Assay

According to the MTT method, the inhibitory activities of 1,4-naphthoquinone derivatives on PC-3 cells, HepG2 cells, K562 cells, and A549 cells were detected after treatment in different concentration ranges (1–30 µM) for 48 h. The specific procedures are as follows: Then, cancer cells at logarithmic growth stage were digested with 0.25% trypsin and re-suspended in DMEM and RPMI culture medium containing 10% FBS. Cancer cells were inoculated into 96-well plates (cell concentration: 2 × 104 cells/mL) at a volume of 100 µL per well, with blank control group on the left. Cell-free RPMI medium with serum was added and placed in an incubator at 37 °C with 5% concentration of carbon dioxide and saturated humidity. Cells were required to be in a state of adherent growth for 24 h. After 24 h, the medium was removed and added to the corresponding hole of the 96-well plate at 200 µL per well (the final concentration of DMSO was less than 0.1%), containing different drugs to be tested. The blank control group was added with 200 µL per well of complete medium. Under the same experimental conditions, 48 h later, the supernatant was poured away, and each well in the 96-well plate was incubated at room temperature (25 °C) for 4 h. DMSO was added to the 96-well plate with 150 µL per well. At room temperature, the cells were shaken by cell shaker for 5 min. The OD value (absorption wavelength 490 nm) was determined with enzyme label, and then the inhibition rate of compound on cells was calculated. Three parallel experiments should be conducted for each sample, with the concentrations of six holes parallel each time, and the calculated average is the final result of the experiment. The relative cell viability was calculated according to the following equation:
Cell   viability ( % ) = experimental   OD   value control   OD   value × 100
Cell   inhibition ( % ) = control   OD   value − experimental   OD   value control   OD   value × 100

4.2.3. Western Blotting Analysis

The 104/well cells in the 6-well plates were cultured for about 24 h and incubated with the compound for 48 h. After cleaning with PBS, cells were added into the mixture of cell lysate RIPA (Beyotime, Shanghai, China), protease inhibitor (Beyotime, Shanghai), and phosphatase inhibitor (Beyotime, Shanghai) 50 μL/well. The cells in the well plates were scraped off with a cell scraper and collected in a small centrifuge tube. The cells were cleaved fully at 4 °C for 1 h. After centrifuging at 4 °C for 15 min (12,000 rpm), supernatant was taken to obtain total cell protein. BCA protein concentration assay kit (Biyuntian, Shanghai) was used to quantify the protein. After incubation at 37 °C for half an hour, the absorbance was measured at 562 nm (in the enzyme marker). Standard diagram (c-OD diagram) was made from 8 protein standards with known concentrations to obtain the required protein sample concentration, which was prepared and marked. Then, they were boiled at 100 °C in a water bath for 10 min for denaturation, and stored at 4 °C for later use. The protein was isolated by SDS-PAGE and then transferred to PVDF membrane. After the membrane transfer was complete, the PVDF membrane was cut according to marker and its molecular weight, immersed in the sealing liquid (5% BSA), and closed at room temperature for 1h with uniform shock (shaking bed 40 rpm). After the closure was complete, the corresponding antibody was added and incubated for 2 h. The antibody could be incubated at 4 °C overnight. Then, the second antibody was added and incubated for 1h. After the incubation, TBST buffer was added 3 times and washed for 5 min each time. According to the size and quantity of the membrane, an appropriate amount of chemiluminescent solution was prepared and dropped on the membrane. The color developed in the gel imager (VilberLourmat), and the data were analyzed by ImageJ software (Version 1.53t 24 August 2022).
The antibodies against EGFR (AF6043, 1:1000) and β-actin (AF7010,1:10,000) were purchased from Affinit. The antibody against LC3 (14600-1-AP, 1:2500) and GAPDH (10494-1-AP, 1:20,000) was purchased from Proteintech. The antibodies against P-EGFR (3777S, 1:1000) and P-AKT (4058T, 1:1000) were purchased from Cell Signaling.

4.2.4. Molecular Docking Study

EGFR (PDBID code: 1M17) eutectic structure model was used for docking. MOE (2019) was used to predict the binding pattern of ligands to the corresponding EGFR (PDBID code: 1M17). Protein structures can be downloaded from the website https://www.rcsb.org (accessed on 1 January 2023) and processed using the protein preparation wizard. The selected compounds were ligands and they were treated with QuickPrep. The whole kinase was used as the receptor and the processed ligand was selected for docking. These image files were generated using MOE (2019).

4.2.5. Statistical Analysis

Statistical processing of results was performed using GraphPad Prism 8.0 software (GraphPad Inc., San Diego, CA, USA). All data were expressed as mean ± SD and all the data provided were verified by at least three independent experiments. Differences among groups were considered significant at p ≤ 0.05.

5. Conclusions

In conclusion, this study reported the synthesis and anti-proliferative activities of two amino-substituted 1,4-naphthoquinone derivatives. Most compounds showed good biological activities on the tested tumor cells, especially compound 5i (IC50 = 6.15 ± 0.19 µM), which exhibited significant anti-proliferation activity against the A549 cells. Based on the preliminary anti-tumor mechanism experimental results, 5i is a promising leading compound that can induce autophagy by promoting EGFR recycling and signal transduction, and therefore, it can provide a new research path for the development of effective autophagy inhibitors.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28083289/s1, Ref. [72] is cited in Supplementary Materials.

Author Contributions

Conceptualization, H.-Y.T., C.-P.L. and D.-P.C.; methodology, H.-Y.T., F.-M.L., C.-P.L. and D.-P.C.; software, H.-Y.T., J.-H.C. and Y.-Y.D.; validation, H.-Y.T., C.-P.L. and D.-P.C.; formal analysis, H.-Y.T. and D.-P.C.; investigation, H.-Y.T. and D.-P.C.; resources, F.-M.L., W.-J.Z., Y.Z. (Yi Zhang), Y.Z. (Yue Zhou), W.-H.W. and X.-M.Q.; data curation, H.-Y.T. and D.-P.C.; writing—original draft preparation, H.-Y.T. and D.-P.C.; writing—review and editing, H.-Y.T. and D.-P.C.; visualization, D.-P.C.; supervision, D.-P.C.; project administration, D.-P.C.; funding acquisition, D.-P.C. All authors have read and agreed to the published version of the manuscript.

Funding

We acknowledge the financial supports of the National Natural Science Foundation of China (22007022), the Science and Technology Foundation of Guizhou Province (ZK [2021]034) and (ZK [2021]049), the Guizhou Provincial Young Science and Technology Talents Development Project (KY [2022]145), the Top Science and Technology Talent Program of Guizhou Education Department ([2022]075), the Guizhou Provincial Department of Education (QjhKYZi [2021]041), the Guizhou University Cultivation Project (GDPY [2019]48), and the Guizhou University Talent Introduction Project (GDRJHZ [2020]6).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lin, L.; Yan, L.; Liu, Y.; Yuan, F.; Li, H.; Ni, J. Incidence and death in 29 cancer groups in 2017 and trend analysis from 1990 to 2017 from the Global Burden of Disease Study. J. Hematol. Oncol. 2019, 12, 1–21. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Bray, F.; Ferlay, J.; Soerjomataram, I.; Siegel, R.L.; Torre, L.A.; Jemal, A. Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. Cancer J. Clin. 2018, 68, 394–424. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Mizushima, N. Autophagy: Process and function. Genes Dev. 2007, 21, 2861–2873. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Mizushima, N. The pleiotropic role of autophagy: From protein metabolism to bactericide. Cell Death Differ. 2005, 12, 1535–1541. [Google Scholar] [CrossRef]
  5. Patan, A.; Göksel, F.S.; Ayla, S.S. Reactions of 2,3-dichloro-1,4-naphthoquinone with piperidine, amine and some thiol nucleophile. Phosphorus. Sulfur. 2021, 196, 647–655. [Google Scholar] [CrossRef]
  6. Pettit, G.R.; Collins, J.C.; Knight, J.C.; Herald, D.L.; Nieman, R.A.; Williams, M.D.; Pettit, R.K. Antineoplastic Agents. 485. Isolation and Structure of Cribrostatin 6, a Dark Blue Cancer Cell Growth Inhibitor from the Marine Sponge Cribrochalinasp. J. Nat. Prod. 2003, 66, 544–547. [Google Scholar] [CrossRef]
  7. El-Najjar, N.; Gali-Muhtasib, H.; Ketola, R.A.; Vuorela, P.; Urtti, A.; Vuorela, H. The chemical and biological activities of quinones: Overview and implications in analytical detection. Phytochem. Rev. 2011, 10, 353–370. [Google Scholar] [CrossRef]
  8. Riffel, A.; Medina, L.; Stefani, V.; Santos, R.; Bizani, D.; Brandelli, A. In vitro antimicrobial activity of a new series of 1,4-naphthoquinones. Braz. J. Med. Biol. Res. 2002, 35, 811–818. [Google Scholar] [CrossRef]
  9. Chen, W.H.; Liu, W.J.; Wang, Y.; Song, X.P.; Chen, G.Y. A new naphthoquinone and other antibacterial constituents from the roots ofXanthium sibiricum. Nat. Prod. Res. 2014, 29, 739–744. [Google Scholar] [CrossRef]
  10. Gokmen, Z.; Onan, M.E.; Deniz, N.G.; Karakas, D.; Ulukaya, E. Synthesis and investigation of cytotoxicity of new N- and S,S-substituted-1,4-naphthoquinone (1,4-NQ) derivatives on selected cancer lines. Synth. Commun. 2019, 49, 3008–3016. [Google Scholar]
  11. Kang, J.; Zhang, P.; Gao, Z.; Zhang, J.; Yan, Z.; Wang, H.; Chen, R. Naphthohydroquinones, naphthoquinones, anthraquinones, and a naphthohydroquinone dimer isolated from the aerial parts of Morinda parvifolia and their cytotoxic effects through up-regulation of p53. Phytochemistry 2016, 130, 144–151. [Google Scholar] [CrossRef]
  12. Yin, Z.-K.; Feng, Z.-M.; Jiang, J.-S.; Zhang, X.; Zhang, P.-C.; Yang, Y.-N. New diterpenoid quinones derived from Salvia miltiorrhiza and their cytotoxic and neuroprotective activities. RSC Adv. 2020, 10, 14235–14242. [Google Scholar] [CrossRef] [Green Version]
  13. Kaewbumrung, S.; Panichayupakaranant, P. Antibacterial activity of plumbagin derivative-richPlumbago indicaroot extracts and chemical stability. Nat. Prod. Res. 2014, 28, 835–837. [Google Scholar] [CrossRef]
  14. Wang, J.; Cheng, Y.; Wu, R.; Jiang, D.; Bai, B.; Tan, D.; Yan, T.; Sun, X.; Zhang, Q.; Wu, Z. Antibacterial Activity of Juglone against Staphylococcus aureus: From Apparent to Proteomic. Int. J. Mol. Sci. 2016, 17, 965. [Google Scholar] [CrossRef] [Green Version]
  15. Tandon, V.K.; Yadav, D.B.; Singh, R.V.; Vaish, M.; Chaturvedi, A.K.; Shukla, P.K. Synthesis and Biological Evaluation of Novel 1,4-Naphthoquinone Derivatives as Antibacterial and Antiviral Agents. J. Cheminform. 2005, 36, 200546093. [Google Scholar] [CrossRef]
  16. Chaudhari, D.; Salunke-Gawali, S.; Chakravarty, D.; Shaikh, S.R.; Lande, D.N.; Gejji, S.P.; Gonnade, R.G. Synthesis and biological activities of imidazole based 1,4-naphthoquinones. New J. Chem. 2020, 44, 6889–6901. [Google Scholar] [CrossRef]
  17. Delarmelina, M.; Daltoe, R.D.; Cerri, M.F.; Madeira, K.P.; Rangel, L.B.A.; Júnior, V.L.; Romão, W.; Taranto, A.G.; Greco, S.J. Synthesis, Antitumor Activity and Docking of 2,3-(Substituted)-1,4-Naphthoquinone Derivatives Containing Nitrogen, Oxygen and Sulfur. J. Braz. Chem. Soc. 2015, 26, 1804–1816. [Google Scholar] [CrossRef]
  18. Kurban, S.; Deniz, N.G.; Sayil, C.; Ozyurek, M.; Guclu, K.; Stasevych, M.; Zvarych, V.; Komarovska-Porokhnyavet, O.; Novikov, V. Synthesis, Antimicrobial Properties, and Inhibition of Catalase Activity of 1,4-Naphtho- and Benzoquinone Derivatives Containing N-, S-, O-Substituted. Heteroat. Chem. 2019, 2019, 1658417. [Google Scholar] [CrossRef]
  19. Deniz, N.G.; Ibis, C.; Gokmen, Z.; Stasevych, M.; Novikov, V.; Komarovska-Porokhnyavets, O.; Özyürek, M.; Guclu, K.; Karakas, D.; Ulukaya, E. Design, Synthesis, Biological Evaluation, and Antioxidant and Cytotoxic Activity of Heteroatom-Substituted 1,4-Naphtho- and Benzoquinones. Chem. Pharm. Bull. 2015, 63, 1029–1039. [Google Scholar] [CrossRef]
  20. Ngoc, T.M.; Phuong, N.T.T.; Khoi, N.M.; Park, S.; Kwak, H.J.; Nhiem, N.X.; Trang, B.T.T.; Tai, B.H.; Song, J.-H.; Ko, H.-J.; et al. A new naphthoquinone analogue and antiviral constituents from the root of Rhinacanthus nasutus. Nat. Prod. Res. 2018, 33, 360–366. [Google Scholar] [CrossRef]
  21. de Mello, C.P.P.; Sardoux, N.S.; Terra, L.; Amorim, L.C.; Vargas, M.D.; da Silva, G.B.; Castro, H.C.; Giongo, V.A.; Madeira, L.F.; Paixão, I.C. Aminomethylnaphthoquinones and HSV-1: In vitro and in silico Evaluations of Potential Antivirals. Antivir. Ther. 2016, 21, 507–515. [Google Scholar] [CrossRef]
  22. Tandon, V.K.; Chhor, R.B.; Singh, R.V.; Rai, S.; Yadav, D.B. Design, Synthesis and Evaluation of Novel 1,4-Naphthoquinone Derivatives as Antifungal and Anticancer Agents. J. Cheminform. 2004, 35, 200424105. [Google Scholar] [CrossRef]
  23. Pingaew, R.; Prachayasittikul, V.; Worachartcheewan, A.; Nantasenamat, C.; Prachayasittikul, S.; Ruchirawat, S.; Prachayasittikul, V. Novel 1,4-naphthoquinone-based sulfonamides: Synthesis, QSAR, anticancer and antimalarial studies. Eur. J. Med. Chem. 2015, 103, 446–459. [Google Scholar] [CrossRef] [PubMed]
  24. Kongkathip, N.; Kongkathip, B.; Siripong, P.; Sangma, C.; Luangkamin, S.; Niyomdecha, M.; Pattanapa, S.; Piyaviriyagul, S.; Kongsaeree, P. Potent antitumor activity of synthetic 1,2-Naphthoquinones and 1,4-Naphthoquinones. Bioorg. Med. Chem. 2003, 11, 3179–3191. [Google Scholar] [CrossRef] [PubMed]
  25. Balachandran, C.; Al-Dhabi, N.A.; Duraipandiyan, V.; Ignacimuthu, S. Bluemomycin, a new naphthoquinone derivative from Streptomyces sp. with antimicrobial and cytotoxic properties. Biotechnol. Lett. 2021, 43, 1005–1018. [Google Scholar] [CrossRef]
  26. Stasevych, M.; Zvarych, V.; Lunin, V.; Deniz, N.G.; Gokmen, Z.; Akgün, O.; Ulukaya, E.; Poroikov, V.; Gloriozova, T.; Novikov, V. Computer-aided prediction and cytotoxicity evaluation of dithiocarbamates of 9,10-anthracenedione as new anticancer agents. SAR QSAR Environ. Res. 2017, 28, 355–366. [Google Scholar] [CrossRef]
  27. Brandão Geraldo, C.; Missias Franciele, C.R.; Arantes, L.M.; Soares, L.F. Antimalarial naphthoquinones. Synthesis via click chemistry, in vitro activity, docking to Pf DHODH and SAR of lapachol-based compounds. Eur. J. Med. Chem. 2018, 145, 191–205. [Google Scholar] [CrossRef]
  28. Zhang, X.-B.; Zou, C.-L.; Duan, Y.-X.; Wu, F.; Li, G. Activity guided isolation and modification of juglone from Juglans regia as potent cytotoxic agent against lung cancer cell lines. BMC Complement. Altern. Med. 2015, 15, 1–8. [Google Scholar] [CrossRef] [Green Version]
  29. Rani, R.; Narasimhan, B.; Varma, R.S.; Kumar, R. Naphthoquinone derivatives exhibit apoptosis-like effect and anti-trypanosomal activity against Trypanosoma evansi. Veter.-Parasitol. 2021, 290, 109367. [Google Scholar] [CrossRef]
  30. Elaridi, J.; Karroum, N.B.; Bouhadir, K.; Fatfat, M.; Gali-Muhtasib, H. preparation and biological evaluation of novel acylhydrazide derivatives of 2,3-dichloronaphthoquinone. Org. Commun. 2017, 10, 122–129. [Google Scholar] [CrossRef]
  31. Lien, J.-C.; Huang, L.-J.; Teng, C.-M.; Wang, J.-P.; Kuo, S.-C. Synthesis of 2-Alkoxy 1,4-Naphthoquinone Derivatives as Antiplatelet, Antiinflammatory, and Antiallergic Agents. Chem. Pharm. Bull. 2002, 50, 672–674. [Google Scholar] [CrossRef] [Green Version]
  32. Salmon-Chemin, L.; Buisine, E.; Yardley, V.; Kohler, S.; Debreu, M.A.; Landry, V.; Davioud-Charvet, E. 2- and 3-Substituted 1,4-Naphthoquinone Derivatives as Subversive Substrates of Trypanothione Reductase and Lipoamide Dehydrogenase fromTrypanosomacruzi: Synthesis and Correlation between Redox Cycling Activities and in Vitro Cytotoxicity. J. Med. Chem. 2001, 44, 548. [Google Scholar] [CrossRef] [PubMed]
  33. Brandelli, A.; Bizani, D.; Martinelli, M.; Stefani, V.; Gerbase, A.E. Antimicrobial activity of 1,4-naphthoquinones by metal complexation. Rev. Bras. Cienc. Solo 2004, 40, 247–253. [Google Scholar] [CrossRef]
  34. Reis, W.J.; Bozzi, Í.A.O.; Ribeiro, M.F.; Halicki, P.C.B.; Ferreira, L.A.; Almeida da Silva, P.E.; da Silva Júnior, E.N. Design of hybrid molecules as antimycobacterial compounds: Synthesis of isoniazid-naphthoquinone derivatives and their activity against susceptible and resistant strains of Mycobacterium tuberculosis. Bioorg. Med. Chem. 2019, 27, 4143–4150. [Google Scholar] [CrossRef]
  35. Jones, S.E.; Grozea, P.N.; Metz, E.N.; Haut, A.; Stephens, R.L.; Morrison, F.S.; Butler, J.J.; Byrne, G.E.; Moon, T.E.; Fisher, R.; et al. Superiority of adriamycin-containing combination chemotherapy in the treatment of diffuse lymphoma.A southwest oncology group study. Cancer 1979, 43, 417–425. [Google Scholar] [CrossRef]
  36. Agrawal, Y.K.; Patel, V.R. Nanosuspension: An approach to enhance solubility of drugs. J. Adv. Pharm. Technol. Res. 2011, 2, 81–87. [Google Scholar] [CrossRef] [PubMed]
  37. Garnier, T.; Mäntylä, A.; Järvinen, T.; Lawrence, J.; Brown, M.; Croft, S. In vivo studies on the antileishmanial activity of buparvaquone and its prodrugs. J. Antimicrob. Chemother. 2007, 60, 802–810. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Alimohammadi, A.; Mostafavi, H.; Mahdavi, M. Thiourea Derivatives Based on the Dapsone-Naphthoquinone Hybrid as Anticancer and Antimicrobial Agents: In Vitro Screening and Molecular Docking Studies. Chemistryselect 2020, 5, 847–852. [Google Scholar] [CrossRef]
  39. Manickam, M.; Boggu, P.R.; Pillaiyar, T.; Nam, Y.J.; Abdullah, M.; Lee, S.J.; Kang, J.S.; Jung, S.-H. Design, synthesis and anticancer activity of 2-amidomethoxy-1,4-naphthoquinones and its conjugates with Biotin/polyamine. Bioorg. Med. Chem. Lett. 2020, 31, 127685. [Google Scholar] [CrossRef]
  40. Manickam, M.; Boggu, P.R.; Cho, J.; Nam, Y.J.; Lee, S.J.; Jung, S.-H. Investigation of chemical reactivity of 2-alkoxy-1,4-naphthoquinones and their anticancer activity. Bioorg. Med. Chem. Lett. 2018, 28, 2023–2028. [Google Scholar] [CrossRef]
  41. Wei, Q.; Wang, X.; Cheng, J.-H.; Zeng, G.; Sun, D.-W. Synthesis and antimicrobial activities of novel sorbic and benzoic acid amide derivatives. Food Chem. 2018, 268, 220–232. [Google Scholar] [CrossRef] [PubMed]
  42. Buysse, A.M.; Yap, M.C.; Hunter, R.; Babcock, J.; Huang, X. Synthesis and biological activity of pyridazine amides, hydrazones and hydrazides. Pest Manag. Sci. 2017, 73, 782–795. [Google Scholar] [CrossRef] [PubMed]
  43. Wiemann, J.; Heller, L.; Csuk, R. Targeting cancer cells with oleanolic and ursolic acid derived hydroxamates. Bioorg. Med. Chem. Lett. 2016, 26, 907–909. [Google Scholar] [CrossRef] [PubMed]
  44. Gholampour, M.; Ranjbar, S.; Edraki, N.; Mohabbati, M.; Firuzi, O.; Khoshneviszadeh, M. Click chemistry-assisted synthesis of novel aminonaphthoquinone-1,2,3-triazole hybrids and investigation of their cytotoxicity and cancer cell cycle alterations. Bioorg. Chem. 2019, 88, 102967. [Google Scholar] [CrossRef] [PubMed]
  45. Suja, T.D.; Divya, K.V.L.; Naik, L.V.; Kumar, A.R.; Kamal, A. Copper-catalyzed three-component synthesis of aminonaphthoquinone–sulfonylamidine conjugates and in vitro evaluation of their antiproliferative activity. Bioorg. Med. Chem. Lett. 2016, 26, 2072–2076. [Google Scholar] [CrossRef] [PubMed]
  46. Sieveking, I.; Thomas, P.; Estévez, J.C.; Quiñones, N.; Cuéllar, M.A.; Villena, J.; Espinosa-Bustos, C.; Fierro, A.; Tapia, R.A.; Maya, J.D.; et al. 2-Phenylaminonaphthoquinones and related compounds: Synthesis, trypanocidal and cytotoxic activities. Bioorg. Med. Chem. 2014, 22, 4609–4620. [Google Scholar] [CrossRef]
  47. Bhasin, D.; Chettiar, S.N.; Etter, J.P.; Mok, M.; Li, P.-K. Anticancer activity and SAR studies of substituted 1,4-naphthoquinones. Bioorg. Med. Chem. 2013, 21, 4662–4669. [Google Scholar] [CrossRef] [Green Version]
  48. Wellington, K.W.; Kolesnikova, N.I. A laccase-catalysed one-pot synthesis of aminonaphthoquinones and their anticancer activity. Bioorg. Med. Chem. 2012, 20, 4472–4481. [Google Scholar] [CrossRef]
  49. Pal, S.; Jadhav, M.; Weyhermüller, T.; Patil, Y.; Nethaji, M.; Kasabe, U.; Salunke-Gawali, S. Molecular structures and antiproliferative activity of side-chain saturated and homologated analogs of 2-chloro-3-(n-alkylamino)-1,4-napthoquinone. J. Mol. Struct. 2013, 1049, 355–361. [Google Scholar] [CrossRef]
  50. Prachayasittikul, V.; Pingaew, R.; Worachartcheewan, A.; Nantasenamat, C.; Prachayasittikul, S.; Ruchirawat, S.; Prachayasittikul, V. Synthesis, anticancer activity and QSAR study of 1,4-naphthoquinone derivatives. Eur. J. Med. Chem. 2014, 84, 247–263. [Google Scholar] [CrossRef]
  51. Benites, J.; Valderrama, J.A.; Bettega, K.; Pedrosa, R.C.; Calderon, P.B.; Verrax, J. Biological evaluation of donor-acceptor aminonaphthoquinones as antitumor agents. Eur. J. Med. Chem. 2010, 45, 6052–6057. [Google Scholar] [CrossRef] [PubMed]
  52. Lisboa, C.D.S.; Santos, V.G.; Vaz, B.G.; de Lucas, N.C.; Eberlin, M.N.; Garden, S.J. C−H Functionalization of 1,4-Naphthoquinone by Oxidative Coupling with Anilines in the Presence of a Catalytic Quantity of Copper(II) Acetate. J. Org. Chem. 2011, 76, 5264–5273. [Google Scholar] [CrossRef] [PubMed]
  53. Pereyra, C.E.; Dantas, R.F.; Ferreira, S.B.; Gomes, L.P.; Silva, F.P., Jr. The diverse mechanisms and anticancer potential of naphthoquinones. Cancer Cell Int. 2019, 19, 207. [Google Scholar] [CrossRef] [Green Version]
  54. Cui, Q.; Tashiro, S.-I.; Onodera, S.; Minami, M.; Ikejima, T. Autophagy Preceded Apoptosis in Oridonin-Treated Human Breast Cancer MCF-7 Cells. Biol. Pharm. Bull. 2007, 30, 859–864. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Iwamaru, A.; Kondo, Y.; Iwado, E.; Aoki, H.; Fujiwara, K.; Yokoyama, T.; Mills, G.B.; Kondo, S. Silencing mammalian target of rapamycin signaling by small interfering RNA enhances rapamycin-induced autophagy in malignant glioma cells. Oncogene 2006, 26, 1840–1851. [Google Scholar] [CrossRef] [Green Version]
  56. Cheng, Y.; Chen, G.; Hu, M.; Huang, J.; Li, B.; Zhou, L.; Hong, L. Has-miR-30a regulates autophagic activity in cervical cancer upon hydroxycamptothecin exposure. Biomed. Pharm. 2015, 75, 67–74. [Google Scholar] [CrossRef]
  57. Schaaf, M.B.E.; Keulers, T.G.; Vooijs, M.A.; Rouschop, K.M.A. LC3/GABARAP family proteins: Autophagy-(un)related functions. FASEB J. 2016, 30, 3961–3978. [Google Scholar] [CrossRef] [Green Version]
  58. Baeken, M.W.; Weckmann, K.; Diefenthäler, P.; Schulte, J.; Yusifli, K.; Moosmann, B.; Behl, C.; Hajieva, P. Novel Insights into the Cellular Localization and Regulation of the Autophagosomal Proteins LC3A, LC3B and LC3C. Cells 2020, 9, 2315. [Google Scholar] [CrossRef]
  59. White, E.; Mehnert, J.M.; Chan, C.S. Autophagy, Metabolism, and Cancer. Clin. Cancer Res. 2015, 21, 5037–5046. [Google Scholar] [CrossRef] [Green Version]
  60. Ravanan, P.; Srikumar, I.F.; Talwar, P. Autophagy: The spotlight for cellular stress responses. Life Sci. 2017, 188, 53–67. [Google Scholar] [CrossRef]
  61. Li, C.-J.; Liao, W.-T.; Wu, M.-Y.; Chu, P.-Y. New Insights into the Role of Autophagy in Tumor Immune Microenvironment. Int. J. Mol. Sci. 2017, 18, 1566. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Galluzzi, L.; Pietrocola, F.; Bravo-San Pedro, J.M.; Amaravadi, R.K.; Baehrecke, E.H.; Cecconi, F.; Codogno, P.; Debnath, J.; Gewirtz, D.A.; Karantza, V.; et al. Autophagy in malignant transformation and cancer progression. EMBO J. 2015, 34, 856–880. [Google Scholar] [CrossRef] [PubMed]
  63. O’Connor, C.J.; Laraia, L.; Spring, D.R. Chemical genetics. Chem. Soc. Rev. 2011, 40, 4332. [Google Scholar] [CrossRef] [PubMed]
  64. Wavhale, R.D.; Martis, E.A.; Ambre, P.K.; Wan, B.; Franzblau, S.G.; Iyer, K.R.; Raikuvar, K.; Macegoniuk, K.; Berlicki, Ł.; Nandan, S.R.; et al. Discovery of new leads against Mycobacterium tuberculosis using scaffold hopping and shape based similarity. Bioorg. Med. Chem. 2017, 25, 4835–4844. [Google Scholar] [CrossRef]
  65. Li, Z.-Z.; Gopala, L.; Tangadanchu, V.K.R.; Gao, W.-W.; Zhou, C.-H. Discovery of novel nitroimidazole enols as Pseudomonas aeruginosa DNA cleavage agents. Bioorg. Med. Chem. 2017, 25, 6511–6522. [Google Scholar] [CrossRef] [PubMed]
  66. Tanaka, A.; Radwan, M.O.; Hamasaki, A.; Ejima, A.; Obata, E.; Koga, R.; Tateishi, H.; Okamoto, Y.; Fujita, M.; Nakao, M.; et al. A novel inhibitor of farnesyltransferase with a zinc site recognition moiety and a farnesyl group. Bioorg. Med. Chem. Lett. 2017, 27, 3862–3866. [Google Scholar] [CrossRef] [PubMed]
  67. Blagg, J.; Workman, P. Choose and Use Your Chemical Probe Wisely to Explore Cancer Biology. Cancer Cell 2017, 32, 268–270. [Google Scholar] [CrossRef] [Green Version]
  68. Zhang, J.-H.; Fan, C.-D.; Zhao, B.-X.; Shin, D.-S.; Dong, W.-L.; Xie, Y.-S.; Miao, J.-Y. Synthesis and preliminary biological evaluation of novel pyrazolo[1,5-a]pyrazin-4(5H)-one derivatives as potential agents against A549 lung cancer cells. Bioorg. Med. Chem. 2008, 16, 10165–10171. [Google Scholar] [CrossRef]
  69. Zheng, L.-W.; Li, Y.; Ge, D.; Zhao, B.-X.; Liu, Y.-R.; Lv, H.-S.; Ding, J.; Miao, J.-Y. Synthesis of novel oxime-containing pyrazole derivatives and discovery of regulators for apoptosis and autophagy in A549 lung cancer cells. Bioorg. Med. Chem. Lett. 2010, 20, 4766–4770. [Google Scholar] [CrossRef]
  70. Abraham, S.A.; Waterhouse, D.N.; Mayer, L.D.; Cullis, P.R.; Madden, T.D.; Bally, M.B. The Liposomal Formulation of Doxorubicin. Liposomes 2005, 391, 71–97. [Google Scholar] [CrossRef]
  71. Rahimipour, S.; Gescheidt, G.; Bilkis, I.; Fridkin, M.; Weiner, L. Towards the Efficiency of Pharmacologically Active Quinoid Compounds: Electron Transfer and Formation of Reactive Oxygen Species. Appl. Magn. Reson. 2009, 37, 629–648. [Google Scholar] [CrossRef]
  72. Li, K.; Yang, K.; Zheng, L.; Li, Y.; Wang, Q.; Lin, R.; He, D. Anti-acute myeloid leukemia activity of 2-chloro-3-alkyl-1,4-naphthoquinone derivatives through inducing mtDNA damage and GSH depletion. Bioorganic Med. Chem. 2018, 26, 4191–4200. [Google Scholar] [CrossRef] [PubMed]
Molecules 28 03289 g001 550
Figure 1. The chemical structures of representative 1,4-naphthoquinone anti-cancer drugs.
Figure 1. The chemical structures of representative 1,4-naphthoquinone anti-cancer drugs.
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Figure 2. Synthetic route of target molecules. Reagents and conditions. (a) K2CO3 and DCM (Dichloromethane) at room temperature. (b) 2-Hydroxy-1,4-naphthoquinone, Cs2CO3, and DMF at room temperature. (c) 3-amino-p-toluidic acid, Cu(OAc)2, and AcOH at 60–70 °C. (d) Different substitution of fatty amines and aromatic amines, HATU, Dipea, and DCM at room temperature.
Figure 2. Synthetic route of target molecules. Reagents and conditions. (a) K2CO3 and DCM (Dichloromethane) at room temperature. (b) 2-Hydroxy-1,4-naphthoquinone, Cs2CO3, and DMF at room temperature. (c) 3-amino-p-toluidic acid, Cu(OAc)2, and AcOH at 60–70 °C. (d) Different substitution of fatty amines and aromatic amines, HATU, Dipea, and DCM at room temperature.
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Figure 3. The crystal structure of compound 5a.
Figure 3. The crystal structure of compound 5a.
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Figure 4. The binding mode of EGFR and compound 5i or Erlotinib. (A) The three-dimensional binding mode of EGFR and compound 5i: compound 5i is orange, residues around the binding bag are displayed in gray, and hydrogen bonds are indicated by dotted lines in light blue. (B) Surface binding mode of EGFR to compound 5i. (C) Two-dimensional binding mode of EGFR and compound 5i. (D) Two-dimensional binding mode of EGFR and Erlotinib.
Figure 4. The binding mode of EGFR and compound 5i or Erlotinib. (A) The three-dimensional binding mode of EGFR and compound 5i: compound 5i is orange, residues around the binding bag are displayed in gray, and hydrogen bonds are indicated by dotted lines in light blue. (B) Surface binding mode of EGFR to compound 5i. (C) Two-dimensional binding mode of EGFR and compound 5i. (D) Two-dimensional binding mode of EGFR and Erlotinib.
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Figure 5. Compound 5i induces ROS accumulation in A549 lung cancer cells. (A) A549 cells were treated with 10 μM and 20 μM 5i at different time points (6 or 12 h) and stained with DCFH-DA (10 μM). Intracellular ROS levels were determined by flow cytometry. (B) A549 cells treated with 10 μM and 20 μM compound 5i at different times (6 or 12 h) were quantitatively analyzed. The values are expressed as mean SD from three individual experiments. * Statistically significant (p < 0.05).
Figure 5. Compound 5i induces ROS accumulation in A549 lung cancer cells. (A) A549 cells were treated with 10 μM and 20 μM 5i at different time points (6 or 12 h) and stained with DCFH-DA (10 μM). Intracellular ROS levels were determined by flow cytometry. (B) A549 cells treated with 10 μM and 20 μM compound 5i at different times (6 or 12 h) were quantitatively analyzed. The values are expressed as mean SD from three individual experiments. * Statistically significant (p < 0.05).
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Figure 6. The effect of 5i on EGFR protein kinase signal pathway. (A) A549 cells were incubated with 5i of different concentrations for 48 h. Gefitinib with a concentration of 10 µM was used as positive control (G-10 µM). Expressions of EGFR, P-EGFR, Akt, and P-Akt were detected by Western blot. (B) Quantify the relative protein expression levels of EGFR, P-EGFR, Akt, and P-Akt. GAPDH is used for load control. The values are expressed as mean SD from three individual experiments. * Statistically significant (p < 0.05). ** Statistically extremely significant (p < 0.01).
Figure 6. The effect of 5i on EGFR protein kinase signal pathway. (A) A549 cells were incubated with 5i of different concentrations for 48 h. Gefitinib with a concentration of 10 µM was used as positive control (G-10 µM). Expressions of EGFR, P-EGFR, Akt, and P-Akt were detected by Western blot. (B) Quantify the relative protein expression levels of EGFR, P-EGFR, Akt, and P-Akt. GAPDH is used for load control. The values are expressed as mean SD from three individual experiments. * Statistically significant (p < 0.05). ** Statistically extremely significant (p < 0.01).
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Figure 7. The effects of 5i on the autophagy-related protein LC3. (A) Western blot analysis of LC3-I and LC3-II of A549 cells treated with 5i (0, 10, and 20 μM) for 48 h. Gefitinib with a concentration of 10 µM was used as positive control (G-10 µM). (B) The relative protein expression levels of LC3-I and LC3-II were quantified by normalization to β-actin. β-actin was used as a loading control. The values are expressed as mean SD from three individual experiments. ** Statistically extremely significant (p < 0.01).
Figure 7. The effects of 5i on the autophagy-related protein LC3. (A) Western blot analysis of LC3-I and LC3-II of A549 cells treated with 5i (0, 10, and 20 μM) for 48 h. Gefitinib with a concentration of 10 µM was used as positive control (G-10 µM). (B) The relative protein expression levels of LC3-I and LC3-II were quantified by normalization to β-actin. β-actin was used as a loading control. The values are expressed as mean SD from three individual experiments. ** Statistically extremely significant (p < 0.01).
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Table
Table 1. The anti-proliferative activity of 1,4-naphthoquinone derivatives on cell carcinoma lines after 48 h treatment.
Table 1. The anti-proliferative activity of 1,4-naphthoquinone derivatives on cell carcinoma lines after 48 h treatment.
CompoundsIC50 ± SD 1 (μM)
RA549K562HepG2PC-3
5a2-CH38.59 ± 0.50---
5b3-CH38.14 ± 0.34---
5c4-CH3> 50---
5d2-Cl20.32 ± 6.43---
5e3-Cl23.45 ± 7.54--14.49 ± 1.38
5f4-Cl> 50---
5g2,4-diCl14.11 ± 1.68---
5h2-F23.59 ± 7.21--34.61 ± 6.45
5i3-F6.15 ± 0.19---
5j4-F19.03 ± 3.8617.79 ± 3.2126.42 ± 3.0518.4 ± 3.46
5k2,4-diF17.23 ± 4.89-20.15 ± 2.49-
5l2,5-diF7.99 ± 1.27-23.59 ± 5.2723.78 ± 5.94
5m3,5-diF6.83 ± 0.7225.61 ± 9.62--
5n2-Br26.58 ± 8.98-23.64 ± 5.089.71 ± 1.87
5o3-Br21.23 ± 3.5526.60 ± 6.18--
5p4-Br8.34 ± 3.1319.53 ± 7.86-10.31 ± 0.82
5q2-OCH310.44 ± 0.52---
5r3-OCH327.76 ± 3.56---
5s4-OCH316.77 ± 2.8129.62 ± 8.90-19.34 ± 4.74
5t2-NO28.45 ± 2.15---
5u3-NO215.64 ± 1.87---
9apropylamine20.32 ± 6.70---
9bbutylamine22.00 ± 3.0621.42 ± 4.0217.90 ± 1.64-
9cphenyl35.55 ± 7.98---
9dcyclopropyl16.54 ± 3.83---
9e2-fluorophenyl14.32 ± 4.18---
9f3-fluorophenyl23.03 ± 4.8124.07 ± 2.67--
9g3-bromophenyl21.31 ± 6.59-22.36 ± 1.4515.49 ± 1.55
G 222.11 ± 2.3215.64 ± 2.5930.67 ± 11.3012.02 ± 5.40
5-Fu 31.34 ± 0.324.01 ± 0.2112.05 ± 5.278.95 ± 0.87
1 IC50 values are the concentrations that cause 50% inhibition of cancer cell growth. Data represent the mean values ± standard deviation of three independent experiments performed in triplicates. 2 Gefitinib (G) is the reference standard. 3 5-Fluorouracil (5-Fu) is the reference standard.
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Tan, H.-Y.; Liang, F.-M.; Zhang, W.-J.; Zhang, Y.; Cui, J.-H.; Dai, Y.-Y.; Qiu, X.-M.; Wang, W.-H.; Zhou, Y.; Chen, D.-P.; et al. Novel 2-Amino-1,4-Naphthoquinone Derivatives Induce A549 Cell Death through Autophagy. Molecules 2023, 28, 3289. https://doi.org/10.3390/molecules28083289

AMA Style

Tan H-Y, Liang F-M, Zhang W-J, Zhang Y, Cui J-H, Dai Y-Y, Qiu X-M, Wang W-H, Zhou Y, Chen D-P, et al. Novel 2-Amino-1,4-Naphthoquinone Derivatives Induce A549 Cell Death through Autophagy. Molecules. 2023; 28(8):3289. https://doi.org/10.3390/molecules28083289

Chicago/Turabian Style

Tan, Hua-Yuan, Feng-Ming Liang, Wen-Jing Zhang, Yi Zhang, Jun-Hao Cui, Yu-Yu Dai, Xue-Mei Qiu, Wen-Hang Wang, Yue Zhou, Dan-Ping Chen, and et al. 2023. "Novel 2-Amino-1,4-Naphthoquinone Derivatives Induce A549 Cell Death through Autophagy" Molecules 28, no. 8: 3289. https://doi.org/10.3390/molecules28083289

APA Style

Tan, H. -Y., Liang, F. -M., Zhang, W. -J., Zhang, Y., Cui, J. -H., Dai, Y. -Y., Qiu, X. -M., Wang, W. -H., Zhou, Y., Chen, D. -P., & Li, C. -P. (2023). Novel 2-Amino-1,4-Naphthoquinone Derivatives Induce A549 Cell Death through Autophagy. Molecules, 28(8), 3289. https://doi.org/10.3390/molecules28083289

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