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Article

Evaluation of the Anticancer Activity and Mechanism Studies of Glycyrrhetic Acid Derivatives toward HeLa Cells

by
Ju Chen
1,†,
Yunran Xu
1,†,
Yan Yang
2,*,
Xin Yao
1,
Yuan Fu
1,
Yi Wang
1,
Yunjun Liu
1,3 and
Xiuzhen Wang
1,*
1
School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China
2
Department of Pharmacy, Guangdong Second Provincial General Hospital, Guangzhou 510317, China
3
Guangdong Provincial Key Laboratory of Advanced Drug Delivery, Guangdong Provincial Engineering Center of Topical Precise Drug Delivery System, Guangdong Pharmaceutical University, Guangzhou 510006, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2023, 28(7), 3164; https://doi.org/10.3390/molecules28073164
Submission received: 26 February 2023 / Revised: 17 March 2023 / Accepted: 31 March 2023 / Published: 2 April 2023
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Abstract

:
In this paper, a series of glycyrrhetic acid derivatives 3a–3f were synthesized via the esterification reaction. The cytotoxicity of these compounds against five tumor cells (SGC-7901, BEL-7402, A549, HeLa and B16) and normal LO2 cells was investigated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. The results showed that compound 3a exhibited high antiproliferative activity against HeLa cells (IC50 = 11.4 ± 0.2 μM). The anticancer activity was studied through apoptosis, cloning, and scratching; the levels of the intracellular ROS, GSH, and Ca2+; and the change in the mitochondrial membrane potential, cell cycle arrest and RNA sequencing. Furthermore, the effects of compound 3a on gene expression levels and metabolic pathways in HeLa cells were investigated via transcriptomics. The experimental results showed that this compound can block the cell cycle in the S phase and inhibit cell migration by downregulating Focal adhesion kinase (FAK) expression. Moreover, the compound can reduce the intracellular glutathione (GSH) content, increase the Ca2+ level and the intracellular ROS content, and induce a decrease in the mitochondrial membrane potential, further leading to cell death. In addition, it was also found that the mechanism of compounds inducing apoptosis was related to the regulation of the expression of mitochondria-related proteins B-cell lymphoma-2 (Bcl-2), Bcl-2-Associated X (Bax), and the activation of the caspase proteins. Taken together, this work provides a help for the development of glycyrrhetinic acid compounds as potential anticancer molecules.

1. Introduction

Pentacyclic triterpenoids are an important class of natural product, and these compounds have a variety of biological activities, thus attracting the in-depth study of scientists [1]. 18β-glycyrrhetinic acid (18β-GA) is a glycyrrhizin aglycone found in the licorice root, which has anti-inflammatory, antiulcer, and antibacterial activities. In addition, 18β-GA has the advantages of easy availability, low cost, good stability, and high biosafety [2,3]. However, the disadvantage of glycyrrhetinic acid (GA) is its weak ability to inhibit tumor cell proliferation [4,5]. To enhance the cytotoxicity of GA, many researchers have synthesized a number of GA derivatives [6,7,8,9,10]. For example, Rui et al. found that the C-30 position of 18β-GA modified with an electron-withdrawing group can improve its toxicity toward tumor cells [11]. Moreover, Csuk et al. performed esterification and amidation reactions on C-30 of GA and the synthesized compounds (esters derivatives) increase cytotoxic activity [12]. These compounds can block the cell cycle and induce apoptosis by modulating the expression of signaling proteins and mitochondrial function [13,14]. The studies on the cytotoxicity show that GA derivatives are potential and promising antitumor drugs [15,16,17,18]. In this study, we used the esterification of GA with different substituent phenol at the para position to synthesize a series of GA derivatives 3a–3f (Scheme 1). Moreover, the synthetic compounds were characterized using HRMS, NMR spectra. To investigate the anticancer activity of compounds 3a–3f, we used the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method to evaluate the cytotoxicity of compounds against several cancer and normal cells. We also studied the apoptotic efficacy of the compounds on HeLa cells and used western blot analysis to detect the expression levels of some apoptosis-related proteins. This study shows that the compounds induce apoptosis through the mitochondrial pathway. Additionally, the effect of the compounds on intracellular gene expression was studied via transcriptomics, and it was discovered that the compounds could affect the metabolic pathways of cells and cause the decrease in the expression of GPX4, which is an important regulator of cellular iron death.

2. Results and Discussion

2.1. Chemistry

The synthetic route of glycyrrhetinic acid derivatives 3a–3f is shown in Scheme 1. Through 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDCI) and 4-dimethylaminopyridine (DMAP)-mediated acylation, the carboxyl group of GA was activated to form amide and ester bonds. Under the catalysis of EDCI and DMAP, 18β-glycyrrhetic acid underwent esterification with p-bromophenol to produce compound 3a at room temperature and was purified via column chromatography using a mixture of EtOAc-petroleum ether (1:3, v/v) as the eluent. The purity of compound 3a was detected via HPLC (COSMOSIL Packed Column 5C18-MS-II 20ID × 250 mm, Model: K1504557) using a mixture of methanol and water (v:v = 95:5) as the mobile phase. In Figure S19 (supporting information), only one peak was observed within 30 min, which indicates that compound 3a is pure and the purity is 99.51%. The melting point of compound 3a was also found to be 205.5–205.9 °C via the capillary method. The molecular weights of these compounds detected in the HRMS spectra were consistent with the expected values. Moreover, the structures of the compounds were also examined using 13C NMR spectra and 1H NMR spectra. In the 1H NMR spectra, the peaks at 3.01, 4.30–4.31, and 5.42–5.45 ppm are assigned to the hydrogen atoms of Ha, Hb, and Hc, respectively. In the 13C NMR spectra, the chemical shifts 199.5, 175.1, 169.5 ppm for 3a, 199.5, 175.1, 169.5 ppm for 3b, 199.4, 175.3, 169.5 ppm for 3c, 199.5, 174.7, 169.4 ppm for 3d, 199.5, 175.3, 169.6 ppm for 3e, and 199.5, 175.5, 169.6 ppm for 3f are assigned to the C (11), C (30), C (13), respectively, while the peaks of 77.0 for 3a–3f are attributed to C (3).

2.2. Cell Viability and IC50 Determination

According to previous reports, the introduction of the ester group at the C-30 site can enhance the biological activity of GA [19,20]. To determine the antitumor activity of compounds 3a–3f, the MTT assay was used to evaluate the anti-proliferative effects of the compounds against five tumor cells and normal LO2 cells. The IC50 values of compounds are listed in Table 1. The anti-proliferative effects of 3a–3d on selected five tumor cells was higher than that of GA (except 3c against BEL-7402). In particular, the IC50 data of compound 3a (IC50 = 11.4 ± 0.2 μM) against HeLa cells were about 6 times greater than that of GA. We also found that the GA derivatives with the electron-withdrawing group such as -X or NO2 possessed a higher ability to inhibit the proliferation of the five types of tumor cells than those with electron-donating groups (such as 3e and 3f). Zheng et al. reported that the benzyl introduced at the C-30 position of GA had an IC50 value of 17.53 μM against HeLa [21]; the introduction of halogen atoms into the compounds showed better antitumor activity [22]. Therefore, the electron-withdrawing group can enhance the activity of the GA derivatives. The cell viability of 3a toward HeLa cells is depicted in Figure 1; the cell viability decreases with increasing concentrations of 3a. Because compound 3a shows the highest ability to suppress HeLa cell growth, we chose compound 3a to study its antitumor mechanism on HeLa cells.

2.3. Apoptosis Studies

To determine whether the compound inhibiting the cell proliferation is attributed to apoptosis in HeLa cells, 4′,6-diamidino-2′-phenylindole (DAPI) staining was used to analyze the cell morphology. The cells were treated with 10 μM, 20 μM, and 30 μM of compound 3a and stained with DAPI, as shown in Figure 2a; the cell morphology in the control group was intact. However, the cells treated with compound 3a, i.e., the apoptotic cells showed apoptotic features such as nuclear shrinkage and chromatin condensation. The morphologic changes of the nuclear cells confirmed that the compound 3a induced the apoptosis. To further evaluate the ability of compound 3a to induce apoptotic cell death, HeLa cells were exposed to compound 3a and the apoptosis was quantitatively analyzed using flow cytometry. As shown in Figure 2b, the percentage of apoptotic cells in the control group is 3.07%, while the apoptotic percentage increased by 4.50% for 10 μM, 4.56% for 20 μM, and 14.23% for 30 μM of 3a compared with that of the control. The results indicate that the compound 3a can effectively induce apoptosis in a dose-dependent manner.

2.4. Inhibition of Cell Migration and Cloning

Cell migration is involved in many biological processes that are closely related to tumor development and metastasis of cancer cells [23,24]. Therefore, the inhibition of cancer cell migration is crucial for the compound exerting anticancer activity. We used scratch experiments to study the effect of compound 3a on cell migration. After treatment of HeLa cells with different concentrations of compound 3a for 24 h, the migration of cells was observed. As shown in Figure 3a, the width in the control group decreased obviously; however, the distance of wounds edge of 3a-treated groups showed less changes compared with the control group. As shown in Figure 3b, the quantification analysis also showed that the percent of wound closure in the different concentration of compound 3a-treated groups were different; 30 μM of 3a showed the highest inhibitory effect on the cell migration. Focal adhesion kinase (FAK) protein plays an important role in the process of cell proliferation [25]; when its expression is blocked, cell invasion and metastasis are inhibited [26]. As shown in Figure 3c,d, the expression level of FAK decreased significantly with the increasing concentration of compound 3a, which further indicated that the compound 3a can effectively inhibit the metastasis of cancer cells. Additionally, the cell cloning was studied; as shown in Figure 3e, after the cells were treated with compound 3a for 10 continuous days, the number of the living cells decreased compared with that in the control, indicating that 3a can prevent the cell colonies formation. The results demonstrated that compound 3a can inhibit the cell migration and colony formation in a dose-dependent manner.

2.5. Cell Cycle Arrest Assay

To evaluate the effect of the compound 3a on cell cycle distribution, HeLa cells were exposed to different concentrations of compound 3a for 24 h and analyzed via flow cytometry. As shown in Figure 4a, compared with the control group, we found that the cell proportion in the S phase increased by 4.56% for 10 µM, 9.65% for 20 µM, and 20.81% for 30 µM, accompanied by a reduction in the G0/G1 phase, which indicated that the compound 3a inhibited the cell proliferation in the S phase in a concentration-dependent manner. In addition, we used western blot to detect the expression level of cell cycle arrest-related proteins (p53, p21), and the results are shown in Figure 4b. Through the quantitative analysis of p53 and p21, the gray values of p53 and p21 proteins showed an upward trend compared with that in the control (Figure 4c), which further verified that the compound 3a blocked the cell cycle in the S phase.

2.6. Determination of Intracellular Reactive Oxygen Species (ROS)

Recent studies have shown that mitochondria are the main source of ROS production in mammalian cells [27]; excessive accumulation of ROS can lead to mitochondrial damage and cell death [28,29]. To demonstrate whether compound 3a can increase intracellular ROS content, we used 2′,7′-dichlorofluorescein diacetate (DCFH-DA) as a fluorescent indicator to analyze the intracellular ROS levels, and Rosup was used as a positive control. As shown in Figure 5a, in the control group, only a weak green fluorescence was detected, while the green fluorescence was significantly enhanced after the cells were treated with different concentration of compound 3a, indicating that compound 3a caused an increase of intracellular ROS levels. Additionally, the quantitative determination of the intracellular ROS levels was performed using flow cytometry (as shown in Figure 5b). Compared with the control group, the DCF fluorescence intensity in the cells increased in a concentration-dependent manner. At low concentration (10 μM), the increase in fluorescence intensity was not obvious, and when the concentration of 3a was 20 μM and 30 μM, the fluorescence intensity of DCF increased to 1.4-fold and 1.8-fold, respectively. These results suggest that compound 3a increases the generation and accumulation of intracellular ROS and triggers apoptosis by disrupting ROS homeostasis.
Excessive ROS production also leads to oxidative stress and activates the mitogen-activated protein kinase (MAPK) signaling pathway [30]. In response to stress, p38MAPK can be activated and phosphorylated [31]. The activation of p38MAPK induces cancer cell apoptosis and inhibits tumor formation [32]. As shown in Figure 5c, we detected the expression of p38MAPK protein using western blot and found that the expression of p38MAPK was upregulated after HeLa cells were treated with compound 3a. The above results suggest that compound 3a causes excess intracellular ROS to lead to oxidative stress and ultimately induce apoptosis, which is associated with the activation of the p38MAPK pathway.

2.7. Effects of Compound on Ca2+ Levels

As a second messenger of various death signal transduction, Ca2+ has an intricate relationship with apoptosis. Elevated levels of intracellular Ca2+ disrupt the mitochondrial membrane potential, and further disrupt the electron transport chain, generate excessive ROS, and eventually lead to apoptosis [33,34]. A Fluo-3AM fluorescent probe was used to examine the effect of compound 3a on intracellular Ca2+ levels. As shown in Figure 6a, the green fluorescence in the control group was very weak, while the bright green fluorescence spots gradually increased after treatment of HeLa cells with different concentrations of compound 3a. As shown in Figure 6b, the intracellular Ca2+ content was significantly higher in the compound 3a-treated group than in the control group. This indicates that compound 3a can increase the level of intracellular Ca2+; therefore, the balance of intracellular Ca2+ is damaged. Excessive intracellular Ca2+ concentration further disrupts mitochondrial function, resulting in the release of cytochromes, which prevents cancer cells from growing.

2.8. Effects on Mitochondrial Membrane Potential

The mitochondria play an important role in both extrinsic and intrinsic apoptosis, and a reduction in the mitochondrial membrane potential (MMP) is considered an early event in apoptotic cells [35,36]. To further investigate whether apoptosis of HeLa cells is related to mitochondrial dysfunction, we determined the change of the mitochondrial membrane potential with 5,5′,6,6′-Tetrachloro-1,1′,3,3′-tetraethyl-imidacarbocyanine iodide (JC-1) as a fluorescent probe. At high MMP, JC-1 emits red fluorescence; at low MMP, JC-1 emits green fluorescence. As shown in Figure 7a, compared with the control, MMP was significantly decreased in HeLa cells treated with cccp (positive control) and different concentrations of compound 3a (10, 20 and 30 μM), manifested by a gradual increase in JC-1 monomer (appeared as green fluorescence, indicating mitochondrial depolarization), while the JC-1 polymer (appeared as red fluorescence, indicating mitochondrial hyperpolarization) gradually decreased. Therefore, compound 3a can induce a decrease in the mitochondrial membrane potential. To further quantify the changes in the mitochondrial membrane potential, we used flow cytometry to measure the ratio of red/green fluorescence intensities. As shown in Figure 7b, the red/green fluorescence ratio in the control group is 2.56; with increasing concentration of compound 3a, the red/green fluorescence ratio gradually decreased. All the above results indicate that compound 3a can significantly induce the decrease in the MMP.

2.9. Analysis of Intracellular GSH Content

It is widely believed that the imbalance between cellular antioxidant capacity and reactive oxygen species (ROS) formation induced by intracellular glutathione (GSH) leads to the death of tumor cells [37,38]. GSH can bind to excess oxygen radicals, and the decrease in GSH levels can lead to increased oxygen radicals in the cell, which can affect normal cell growth. [39,40]. As shown in Figure 8a, the intracellular GSH content in the control is 57.7; after HeLa cells were treated with compound 3a for 24 h, a decrease in the intracellular GSH content of 10.4% for 10 μM, 18.2% for 20 μM, and 24.3% for 30 μM was observed. In Figure 8b, the ratio of GSH/GSSG (glutathione disulfide) was determined. In the control, the ratio of GSH/GSSG is 9.9; after an exposure of HeLa cells to 10, 20, and 30 μM of compound 3a for 24 h, the ratios of GSH/GSSG reduced compared with that in the control. Therefore, compound 3a can reduce the content of intracellular GSH and cause an increase in oxidant stress.

2.10. Differential Gene Expression Level Analysis

To investigate the antitumor mechanism of compound 3a, the effect on transcriptional genomic expression of HeLa cells was assayed through high-throughput sequencing. In the differential gene expression statistics and volcano (Figure 9a,b), compound 3a could affect the expression of 50 genes, in which the expression of 31 genes was downregulated and 19 genes were upregulated. KEGG metabolic pathway analysis (Figure 9c) showed that these differential genes were mainly enriched in phagosomes, iron death, primary immunodeficiency, and some biometabolic processes. The GO enrichment analysis showed that the biological processes were regulated by these differential genes as well as their molecular functions (Figure 9d). This further demonstrated that compound 3a affected the activity of some intracellular nucleotide receptors and intracellular signaling including G protein-coupled receptor signaling pathway, intracellular production of some factors and other biological processes. In addition, the above results suggest that the anticancer activity may be related to processes including cytokine secretion, glycoconjugate metabolism, signaling, and iron death of cells.

2.11. Western Blot Detection

To further explore the molecular mechanism of apoptosis, the effect of compound 3a on the apoptosis-related protein was investigated using western blot. According to literature, the BH3 family of proteins plays a crucial role in the regulation of intrinsic apoptotic pathways [41]. After the cells are stimulated by apoptotic factors, the various apoptotic signals can be activated and the change in the expression of corresponding proteins, including pro-apoptotic proteins (Bax, Bad) and anti-apoptotic proteins (Bcl-2), is observed. The expression of Bax protein induces the opening of transport pores in the mitochondrial membrane to release cytochrome C, which binds to apoptotic protein activating factor (Apaf-1) and activates caspase-9. The activated caspase-9 further activates caspase-7 and caspase-3. The activated caspase-3 can cleave the cellular substrate PARP, eventually leading to apoptosis [42]. As shown in Figure 10a,b, we found that compound 3a significantly upregulated the expression of the pro-apoptotic protein Bax, while downregulating the expression of the anti-apoptotic protein Bcl-2 compared with that in the control. Furthermore, after HeLa cells were treated with compound 3a for 24 h, the apoptosis-executing protein caspase-3 was activated, resulting in upregulation of its downstream molecule caspase-7 and increased cleavage of PARP. RNA sequencing experiments show that compound 3a can also induce iron death in HeLa cells. It is well known that the marker of iron death is the inactivation of GPX4 [43], so we also detected the effect of compound 3a on the expression level of GPX4 using protein blotting experiments. As observed in Figure 10, compound 3a downregulated the expression of GPX4 protein, indicating that compound 3a caused iron death in tumor cells; this is consistent with the results of KEGG metabolic pathway analysis.

3. Materials and Methods

3.1. Materials

A Bruker AVANCE-500 spectrometer was used to detect NMR spectra. All chemical shifts were given relative to tetramethylsilane (TMS). Bruker 7.0 T SolariX XR FT-ICR-MS was used to record mass spectra. TLC-analysis was performed on glass-backed plates (Sigma-Aldrich, Canada) coated with 0.2 mm silica 60F254. Commercial common reagent-grade chemicals were used without further purification. The gastric adenocarcinoma cell line SGC-7901, cervical cancer cell line HeLa, lung carcinoma cell line A549, human hepatocellular carcinoma cell line BEL-7402, and normal live cell line LO2 were purchased from the cell bank of the Cell Institute of Sinica Academia Shanghai (Shanghai, China). Buffers were prepared using doubly distilled water. The 4′,6-diamidino-2′-phenylindole (DAPI), cell cycle and apoptosis analysis kits were purchased from Beyotime (Shanghai, China). 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) was obtained from Sigma–Aldrich. The fluorescent dye 2′,7′-dichlorodihydrofluorescein diacetate (DCHF-DA) and 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolcarbocyanine iodide (JC-1) were purchased from Roche Diagnostics (Indianapolis, IN, USA). Polyclonal antibodies against Bcl-2, Bax, and P38 were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Caspase-3 antibodies were purchased from Cell Signaling Technology (Beverly, MA, USA).

3.2. Synthesis of Compounds

A mixture of 18β-glycyrrhetinic acid (18-GA) (0.471 g, 1 mmol), 4-dimethylaminopyridine (DMPA) (0.214 g, 1 mmol), and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDCI) (0.283 g, 1.5 mmol) in dichloromethane (DCM) was stirred for 30 min; then, substituent phenol (1 mmol) was added and stirred for 12 h at room temperature. Thin layer chromatography (TCL) was used to monitor the reaction. The mixture was extracted in DCM. The organic phase was dried over using MgSO4. The solvent was removed, and the crude product was purified via column chromatography on silica gel (100–200 mesh) with a mixture of EtOAc-petroleum ether (1:3, V/V) as the eluent; a white power was obtained.
4-Bromophenyl 3β-hydroxy-11-oxo-olean-12-en-30-oate (3a): Yield 61.2%, 1H-NMR (500 MHz, DMSO-d6) (Figure S1, supporting information): δ 7.62 (d, J = 8.5 Hz, 2H, Ar-H), 7.10 (d, J = 8.5 Hz, 2H, Ar-H), 5.43 (s, 1H), 4.31 (s, 1H), 3.01 (t, 1H, J = 6.0 Hz, 1H), 2.64–2.50 (m, 4H), 2.36–2.33 (m, 2H), 2.13–2.11 (m, 3H), 1.95–1.77 (m, 6H), 1.65–1.63 (m, 2H), 1.59–1.50 (m, 4H), 1.19–1.16 (m, 2H), 1.10–1.05 (m, 6H), 1.02–0.91 (m, 6H), 0.90–0.82 (m, 3H), 0.81–0.68 (m, 4H). 13C-NMR (125 MHz, DMSO-d6) (Figure S2, supporting information): 199.5, 175.1, 169.5, 150.2, 132.9 (2C), 127.9, 124.5(2C), 118.6, 77.0, 61.6, 54.5, 48.6, 45.3, 44.3, 43.3, 40.1, 39.9, 39.8, 37.7, 37.1, 32.5, 32.1, 30.6, 28.6, 28.5, 27.8, 27.4, 26.5, 26.1, 23.4, 18.8, 18.4, 17.9, 17.6. HRMS (solvent) calcd for C36H49BrNaO4+: m/z = 647.2712 ([M + Na]+), found: m/z = 647.2517 (Figure S3, supporting information).
4-Chlorophenyl 3β-hydroxy-11-oxo-olean-12-en-30-oate (3b): Yield 65.3%, 1H-NMR (500 MHz, DMSO-d6) (Figure S4, supporting information): δ 7.50 (d, J = 8.5 Hz, 2H, Ar-H), 7.19–7.15 (m, 2H, Ar-H), 5.43 (s, 1H), 4.31 (s, 1H), 3.01 (t, 1H, J = 6.0 Hz, 1H), 2.63 (s, 1H), 2.58–2.55 (m, 2H), 2.37–2.33 (m, 2H), 2.19–2.12 (m, 3H), 1.97–1.73 (m, 6H), 1.69–1.62 (m, 1H), 1.59–1.50 (m, 4H), 1.48–1.42 (m, 2H), 1.39–1.31 (m, 4H), 1.18–1.14 (m, 2H), 1.11–0.92 (m, 6H), 0.91–0.81 (m, 4H), 0.80–0.69 (m, 5H). 13C-NMR (125 MHz, DMSO-d6) (Figure S5, supporting information): 199.5, 175.1, 169.5, 156.7, 149.7, 130.4, 130.0, 129.5, 127.9, 124.1, 122.7, 117.3, 77.0, 61.6, 54.5, 48.5, 45.3, 44.3, 43.3, 40.1, 39.9, 39.8, 37.7, 37.1, 32.5, 32.1, 30.6, 28.6, 28.5, 27.8, 27.4, 26.5, 26.1, 23.4, 18.7, 17.6. HRMS (CH3OH) calcd for C36H49ClNaO4+: m/z = 603.3217 ([M + Na]+), found: m/z = 603.2985 (Figure S6, supporting information).
4-Fluorophenyl 3β-hydroxy-11-oxo-olean-12-en-30-oate (3c): Yield 65.3%, 1H-NMR (500 MHz, DMSO-d6) (Figure S7, supporting information): δ 7.26 (d, J = 8.5 Hz, 2H), 7.15 (t, J = 4.5 Hz, 2H), 5.43 (s, 1H), 4.31 (s, 1H), 3.01 (t, 1H, J = 6.0 Hz, 1H), 2.59–2.48 (m, 3H), 2.37–2.33 (m, 2H), 2.19–2.11 (m, 2H), 1.98–1.73 (m, 4H), 1.69–1.62 (m, 1H), 1.60–1.51 (m, 4H), 1.46–1.32 (m, 5H), 1.18–1.14 (m, 1H), 1.12–1.02 (m, 8H), 0.97–0.92 (m, 4H), 0.89–0.81 (m, 4H), 0.78–0.71 (m, 4H). 13C-NMR (125 MHz, DMSO-d6) (Figure S8, supporting information): 199.4, 175.3, 169.5, 161.0, 159.1, 147.0, 127.9, 124.0, 123.9, 116.7, 116.5, 77.0, 61.6, 54.5, 48.5, 45.3, 44.3, 40.1, 39.9, 39.8, 37.1, 32.5, 32.1, 30.6, 28.6, 28.5, 27.8, 27.4, 26.9, 26.5, 26.1, 23.4, 18.7, 17.6, 16.5, 16.4. HRMS (CH3OH) calcd for C36H49FNaO4+: m/z = 587.3513 ([M + Na]+), found: m/z = 587.3310 (Figure S9, supporting information).
4-Nitrophenyl 3β-hydroxy-11-oxo-olean-12-en-30-oate (3d): Yield 65.3%, 1H-NMR (500 MHz, DMSO-d6) (Figure S10, supporting information): δ 8.32 (d, J = 9.0 Hz, 2H, Ar-H), 8.11 (d, J = 9.0 Hz, 2H, Ar-H), 5.45 (s, 1H), 4.31 (s, 1H), 3.01 (t, 1H, J = 6.0 Hz, 1H), 2.58–2.55 (m, 1H), 2.38–2.34 (m, 2H), 2.21–2.13 (m, 2H), 1.96–1.77 (m, 4H), 1.67–1.44 (m, 4H), 1.42–1.35 (m, 16H), 1.19–1.14 (m, 1H), 1.10–1.02 (m, 6H), 0.96–0.88 (m, 2H), 0.87–0.79 (m, 2H), 0.78–0.65 (m, 2H). 13C-NMR (125 MHz, DMSO-d6) (Figure S11, supporting information): 199.5, 174.7, 169.4, 164.4, 155.9, 145.6, 128.0, 126.6, 125.8 (2C), 123.6 (2C), 116.2, 77.0, 61.6, 54.5, 48.5, 45.3, 44.5, 43.3, 39.9, 37.1, 32.5, 32.1, 30.5, 28.6, 28.5, 27.7, 27.4, 26.5, 26.1, 23.4, 18.7, 17.6, 16.6, 16.4. HRMS (CH3OH) calcd for C36H49NNaO6+: m/z = 614.3412 ([M + Na]+), found: m/z = 614.3244 (Figure S12, supporting information).
p-Tolyl 3β-hydroxy-11-oxo-olean-12-en-30-oate (3e): Yield 67.3%, 1H-NMR (500 MHz, DMSO-d6) (Figure S13, supporting information): δ 7.23 (d, J = 8.5 Hz, 2H, Ar-H), 6.96 (d, J = 8.5 Hz, 2H, Ar-H), 5.42 (s, 1H), 4.30 (s, 1H), 3.01 (t, 1H, J = 6.0 Hz, 1H), 2.64–2.63 (m, 1H), 2.58–2.54 (m, 2H), 2.38–2.31 (m, 4H), 2.18–2.11 (m, 2H), 1.98–1.75 (m, 4H), 1.69–1.62 (m, 1H), 1.59–1.43 (m, 4H), 1.41–1.28 (m, 8H), 1.21–1.14 (m, 1H), 1.08–1.01 (m, 6H), 0.99–0.91 (m, 4H), 0.89–0.83 (m, 4H), 0.81–0.72 (m, 4H). 13C-NMR (125 MHz, DMSO-d6) (Figure S14, supporting information): 199.5, 175.3, 169.6, 1 48.8, 135.4, 130.4 (2C), 127.9, 121.7 (2C), 77.0, 61.6, 54.5, 48.6, 45.3, 44.2, 43.3, 39.9, 37.8, 37.1, 32.5, 32.1, 30.7, 29.2, 28.7, 28.5, 27.8, 27.4, 26.5, 26.4, 26.2, 23.4, 20.8, 18.8, 18.5, 17.8, 17.6. HRMS (CH3OH) calcd for C37H52NaO4+: m/z = 583.3763 ([M + Na]+), found: m/z = 583.3676 (Figure S15, supporting information).
4-Methoxyphenyl 3β-hydroxy-11-oxo-olean-12-en-30-oate (3f): Yield 63.6%, 1H-NMR (500 MHz, DMSO-d6) (Figure S16, supporting information): δ 7.01–6.95 (m, 4H), 5.42 (s, 1H), 4.31 (s, 1H), 3.78–3.75 (m, 3H), 3.01 (t, 1H, J = 6.0 Hz, 1H), 2.58–2.54 (m, 1H), 2.36–2.34 (m, 1H), 2.18–2.12 (m, 2H), 1.97–1.72 (m, 4H), 1.68–1.62 (m, 1H), 1.57–1.44 (m, 4H), 1.43–1.25 (m, 12H), 1.19–1.14 (m, 1H), 1.08–1.02 (m, 9H), 1.01–0.92 (m, 3H), 0.91–0.82 (m, 2H), 0.80–0.71 (m, 2H). 13C-NMR (125 MHz, DMSO-d6) (Figure S17, supporting information): 199.5, 175.5, 169.6, 157.3, 144.3, 127.8, 122.8 (2C), 115.0 (2C), 77.0, 61.6, 55.9, 54.5, 48.6, 45.3, 44.2, 43.3, 40.1, 42.5, 39.9, 37.8, 37.1, 32.5, 32.1, 30.7, 28.7, 28.5, 27.8, 27.4, 26.5, 26.2, 23.4, 18.8, 17.6, 16.6, 16.4. HRMS (CH3OH): calcd for C37H52NaO5+: m/z = 599.3712 ([M + Na]+), found: m/z = 599.3566 (Figure S18, supporting information).

3.3. Purity Determination of the Compound

The purity of compound 3a was analyzed on a COSMOSIL 5C18-MS-II column (250 mm × 10 mm) at 25 °C. We used H2O containing 0.1% trifluoroacetic acid (TFA) as mobile phase A and methanol containing 0.1% TFA as mobile phase B, with a flow rate of 3 mL/min. The elution program of compound 3a was H2O (0.1% TFA): MeOH (0.1% TFA) = 5:95, and the detection wavelengths were set to 251 nm and 254 nm.

3.4. Cell Viability Assay

The effects of compounds on cells proliferation were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. It is based on the ability of succinate dehydrogenase in living cells to reduce MTT to an insoluble purple formamide precipitate, while dead cells do not [44]. The cells were placed in 96-well plates and treated overnight at 37 °C and 5% CO2. When the cells grew to about 80%, they were treated with different concentrations of compound 3a for 48 h. Then, the culture medium was removed and MTT solution was added. After 4 h, the absorbance values were measured at 490 nm. In addition, the IC50 values were calculated with SPSS (Statistical Product and Service Solutions).

3.5. DAPI Studies Apoptotic Morphology

4′,6-diamidino-2′-phenylindole (DAPI) can enter cells through the cell membrane and dye the nucleus blue, which is used to detect the changes in the cell nuclear morphology. Normal nuclei are round and the chromatin is uniform, while the nuclei of apoptotic cells shrink and the cell outline is not clear [45]. HeLa cells were treated with compound 3a for 24 h and fixed with paraformaldehyde for 15 min. The cells were stained with DAPI solution for half an hour and washed three times with PBS. Then the cells were photographed under ImageX-press R Micro XLS System (MD company, San Jose, CA, USA).

3.6. Apoptosis Was Detected Using Flow Cytometry

After incubating the cells in 6-well plates for one day, a concentration gradient of compound 3a was added for 24 h. The cells were washed twice with PBS and then digested by adding trypsin. The supernatant was removed via centrifugation, and Annexin V-FITC buffer and Annexin-FITC solution were added. The percentage of the apoptotic cells was detected on a FACS Calibur flow cytometer (Beckman Dickinson & Co., Franklin Lakes, NJ, USA).

3.7. Wound Healing Migration Assay

HeLa cells (5.5 × 105) were seeded in a 6-well plate and incubated for one day; they were then scratched and traced with the tip of a clean pipette. After washing the cells three times with PBS to remove the residue, a concentration gradient of compound 3a was added for 24 h. Finally, after washing the cells twice with PBS, the migration of the cells was observed under an optical microscope and photographed.

3.8. Colony Formation Assay

HeLa cells (5.5 × 105) were seeded in 6-well plates and placed in the incubator overnight, and the cells were treated with different concentrations of compound 3a for 24 h. Then, the culture medium was replaced with fresh culture medium. The cells were grown for ten consecutive days; then, the culture medium was removed and the cells were washed twice with PBS. Finally, the cells were fixed with 4% paraformaldehyde solution for 30 min and stained with crystal violet (5%, w/v) for 30 min; the cells were observed under a light microscope and recorded.

3.9. Cell Cycle Arrest Assay

HeLa cells (5.5 × 105) were spread in 6-well plates overnight; the cells were treated with different concentration of compound 3a for 24 h. The cells were then washed twice with PBS and digested with trypsin. The supernatant was removed via centrifugation and fixed overnight in 70% ethanol. The cells were washed twice with PBS and resuspended in a 190 μL staining buffer containing 4 μL of 1 mg/mL PI (propidium iodide), 4 μL of 10 mg/mL RNaseA (ribonuclease), and 0.2 μL Tritonx-100. After staining for 20 min in the dark, the cell cycle distribution was detected using flow cytometry (Beckman Dickinson & Co., Franklin Lakes, NJ, USA) [46].

3.10. Determination of Intracellular Reactive Oxygen Species (ROS)

HeLa cells (5.5 × 105) were spread in 12-well plates and incubated at 37 °C in 5% CO2 overnight. After treatment of HeLa with different concentrations of compound 3a for 24 h, the culture medium in the wells was removed and the cells were washed twice with PBS. The cells were then stained with 20 μM 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) in the dark for 30 min. Finally, the cells were observed under the ImageXpress Mico XLS system (MD company, San Jose, CA, USA) and the intracellular reactive oxygen species content was determined under flow cytometry (Beckman Dickinson & Co., Franklin Lakes, NJ, USA).

3.11. Effects of Compound on Ca2+ Levels

HeLa cells (5.5 × 105) were spread in a 6-well plate and incubated for 24 h; then, the cells were treated with different concentrations of compound 3a for 24 h, and the cells were stained with the fluorescent probe Fluo-3 AM for 20 min and washed three times with PBS. Moreover, the nuclei were stained with DAPI in the dark for 30 min. Finally, the cells were observed under a fluorescence microscope (MD company, San Jose, CA, USA). Furthermore, the level of intracellular Ca2+ was quantified using flow cytometry (Beckman Dickinson & Co., Franklin Lakes, NJ, USA).

3.12. Effects on Mitochondrial Membrane Potential

Exponential growth phase HeLa cells were seeded into 12-well plates overnight. After the treatment of HeLa with different concentrations of compound 3a for 24 h, the cells were then washed twice with PBS and stained with 200 μL of 5,5′,6,6′-Tetrachloro-1,1′,3,3′-tetraethyl-imidacarbocyanine iodide (JC-1) in the dark for 30 min; the cells were washed with PBS to remove residual dye solution. Then, the cells were photographed under a fluorescence microscope (MD company, San Jose, CA, USA) and the intensities of red and green fluorescence were measured with flow cytometry (Beckman Dickinson & Co., Franklin Lakes, NJ, USA).

3.13. Detection of Intracellular GSH Levels

HeLa cells (5.5 × 105) were spread in 6-well plates, and intracellular GSH was detected using the GSH and GSSG assay kits (Beyotime, Biotechnology, China). The cells were digested down with trypsin after treatment with compound 3a. Afterwards, the cells were lysed using the freeze-thaw method, and the lysate was centrifuged for 5 min to collect the supernatant. The absorbance was measured at 412 nm with a microplate reader, and then the GSH content was calculated.

3.14. Transcriptome Analysis

HeLa cells (5.5 × 105) were spread in 6-well plates and placed in an incubator at 37 °C for 24 h. The cells were treated twice with IC50 concentration of compound 3a for 24 h. The cells were then washed twice with pre-cooled PBS. An appropriate amount of RNA extract (Servicebio, China) was added, and the cells were fully lysed by blowing the liquid several times with a pipetting gun. Trizol reagent (Invitrogen Life Technologies, CA, USA) was then added to extract total RNA, and the concentration, quality and integrity of RNA were measured using NanoDrop spectrophotometer (Thermo Scientific, MA, USA). RNA sequence libraries were generated using the TruSeq RNA sample preparation kit (lllumina, San Diego, CA, USA). The library was also optimized using the AMpureXP system (Beckman Coulter, Beverly, CA, USA) to choose cDNA fragments of 200 bp in length. Moreover, the library fragments were quantified using Agilent high-sensitivity DNA analysis on a BioAnalyst 2100 system (Agilent, Santa Clara, CA, USA). Finally, the sequencing library was sequenced on the Hiseqplatform (lllumina) by Shanghai Personal Biotechnology Co., Ltd (Shanghai, China).

3.15. Western Blot Detection

After HeLa cells (5.5 × 105) were seeded in 6-well plates and incubated for 24 h, the cells were treated with different concentrations of compound 3a. Then, the cells were lysed with lysis buffer and centrifuged, and the protein concentration of each sample supernatant was measured with the BCA (bicinchoninic acid) assay. Load the sample protein in equal amount, and stop the sodium dodecyl sulfate-polyacrylamide gel electrophoresis after the bands are separated. The gel was transferred to poly (vinylidene difluoride) membranes (Millipore, Billerica, MA, USA) and blocked with 5% nonfat milk in TBST (20 mM Tris-HCl, 150 mM NaCl, 0.05% Tween 20, pH 8.0, Tween: polyoxyethylene monolaurate sorbaitan) buffer for 1 h. The polyvinylidene fluoride membranes were washed with TBST and incubated with the corresponding primary antibody overnight in a refrigerator at 4 °C. The secondary antibodies were then conjugated with horseradish peroxidase (1:1000 dilution) for 60 min at room temperature. Finally, the blots were visualized with the Amersham ECL (electrochemiluminescence) and western blotting detection reagents according to the manufacturer’s instructions.

3.16. Statistical Analysis

All data were expressed as the mean ± SD. Differences between two groups were analyzed using a two-tailed Student’s test. Differences with * p < 0.05 were considered statistically significant.

4. Conclusions

In this study, six GA analogs were synthesized and characterized using HRMS, 1H NMR and 13C NMR. In vitro cytotoxicity of compounds was carried out using the MTT assay, and the results of cloning experiments and scratch assay showed that compound 3a resulted in an obvious inhibitory effect on the proliferation and migration of HeLa cells. The apoptotic assays confirmed that compound 3a could induce apoptosis of HeLa cells. In the apoptosis mechanism diagram (Figure 11), Compound 3a promotes an increase in intracellular Ca2+ levels and a decrease in GSH levels, leading to an increase in intracellular ROS content, which further resulted in impaired mitochondrial function, including a decrease in mitochondrial membrane potential and an increase in the protein ratio of Bax/Bcl-2. In addition, compound 3a upregulated the expression of cell cycle arrest-related proteins p53 and p21, caused DNA damage, and activated the p53/p21 signaling pathway, leading to cell death by arresting in the S phase. Taken together, compound 3a induced apoptosis in HeLa via the ROS-mediated mitochondrial dysfunction pathway. This work provides help for designing and synthesizing GA derivatives as potent anticancer candidate reagents.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28073164/s1, Compound 3a: Figure S1 for 1H NMR, Figure S2 for 13C NMR, Figure S3 for HRMS; Compound 3b: Figure S4 for 1H NMR, Figure S5 for 13C NMR, Figure S6 for HRMS spectra, Compound 3c: Figure S7 for 1H NMR, Figure S8 for 13C NMR, Figure S9 for HRMS; Compound 3d: Figure S10 for 1H NMR, Figure S11 for 13C NMR, Figure S12 for HRMS spectra, Compound 3e: Figure S13 for 1H NMR, Figure S14 for 13C NMR, Figure S15 for HRMS; Compound 3f: Figure S16 for 1H NMR, Figure S17 for 13C NMR, Figure S18 for HRMS spectra, Figure S19 Determination of the purity of 3a using HPLC.

Author Contributions

Conceptualization, J.C. and Y.F.; methodology, Y.F. and X.Y.; soft, Y.F. and Y.X.; validation, J.C. and Y.X.; formal analysis, X.Y. and Y.W.; investigation, J.C. and Y.X.; resources, Y.F. and J.C.; data curation, Y.W. and X.W.; writing—original draft preparation, J.C., Y.Y. and X.W.; writing-review and editing, Y.L.; funding acquisition, Y.L. and X.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funding by the Natural Science foundation of Guangdong Province (No. 2020A1515010524) and the National Natural Science Foundation of China (No. 21877018).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data are available in the manuscript and Supplementary Materials.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the compounds 3a–3f are available from the authors.

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Molecules 28 03164 sch001 550
Scheme 1. The synthetic route of 3a–3f.
Scheme 1. The synthetic route of 3a–3f.
Molecules 28 03164 sch001
Molecules 28 03164 g001 550
Figure 1. The cell viability of HeLa treated with different concentrations of 3a for 48 h.
Figure 1. The cell viability of HeLa treated with different concentrations of 3a for 48 h.
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Figure 2. (a) DAPI nuclear staining of HeLa cells treated with different concentrations of compound 3a for 24 h. (b) Apoptosis rate of HeLa cells was detected using flow cytometry after HeLa cells were treated with different concentration of compound 3a for 24 h.
Figure 2. (a) DAPI nuclear staining of HeLa cells treated with different concentrations of compound 3a for 24 h. (b) Apoptosis rate of HeLa cells was detected using flow cytometry after HeLa cells were treated with different concentration of compound 3a for 24 h.
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Figure 3. (a) The wound healing assay after HeLa cells were treated with different concentrations of compound 3a for 24 h. (b) Wound closure ratio values. (c) The expression of FAK and β-actin was used as the internal control. (d) Quantitative analysis of FAK protein expression. (e) Cell colonies of HeLa treated with compound 3a for continuous 10 days.
Figure 3. (a) The wound healing assay after HeLa cells were treated with different concentrations of compound 3a for 24 h. (b) Wound closure ratio values. (c) The expression of FAK and β-actin was used as the internal control. (d) Quantitative analysis of FAK protein expression. (e) Cell colonies of HeLa treated with compound 3a for continuous 10 days.
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Molecules 28 03164 g004a 550Molecules 28 03164 g004b 550
Figure 4. (a) Distribution of cell cycle of HeLa cells incubated with different concentrations of compound 3a (control (I), 10 µM (II), 20 µM (III), and 30 µM (IV)) for 24 h. (b) Western blotting analysis of p53 and p21 proteins in HeLa cells treated with different concentrations of compound 3a for 24 h. β-actin was used as the internal control. (c) Quantitative analysis of p53 and p21 protein expression.
Figure 4. (a) Distribution of cell cycle of HeLa cells incubated with different concentrations of compound 3a (control (I), 10 µM (II), 20 µM (III), and 30 µM (IV)) for 24 h. (b) Western blotting analysis of p53 and p21 proteins in HeLa cells treated with different concentrations of compound 3a for 24 h. β-actin was used as the internal control. (c) Quantitative analysis of p53 and p21 protein expression.
Molecules 28 03164 g004aMolecules 28 03164 g004b
Molecules 28 03164 g005 550
Figure 5. (a) Production of ROS in HeLa cells treated with different concentrations of compound 3a for 24 h was assayed. (b) Quantitative determination of DCF fluorescence intensity using flow cytometry (I) control group; (II) Rosup (a positive control); (III) 10 μM; (IV) 20 μM; (V) 30 μM of 3a. (c) The expression of p38MAPK after HeLa cells were exposed to 3a for 24 h. (d) Quantitative analysis of p38MAPK protein expression.
Figure 5. (a) Production of ROS in HeLa cells treated with different concentrations of compound 3a for 24 h was assayed. (b) Quantitative determination of DCF fluorescence intensity using flow cytometry (I) control group; (II) Rosup (a positive control); (III) 10 μM; (IV) 20 μM; (V) 30 μM of 3a. (c) The expression of p38MAPK after HeLa cells were exposed to 3a for 24 h. (d) Quantitative analysis of p38MAPK protein expression.
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Figure 6. (a) Intracellular Ca2+ levels were assayed after HeLa cells were exposed to different concentration of 3a for 24 h. (b) Quantification of intracellular Ca2+ levels.
Figure 6. (a) Intracellular Ca2+ levels were assayed after HeLa cells were exposed to different concentration of 3a for 24 h. (b) Quantification of intracellular Ca2+ levels.
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Figure 7. (a) The mitochondrial membrane potential detection of HeLa cells treated with 3a for 24 h. (b) The ratio of red/green fluorescence intensity in HeLa cells.
Figure 7. (a) The mitochondrial membrane potential detection of HeLa cells treated with 3a for 24 h. (b) The ratio of red/green fluorescence intensity in HeLa cells.
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Figure 8. (a) Analysis of intracellular GSH content after 24 h exposure of HeLa to different concentration of compound 3a. (b) Quantification of the ratio of GSH/GSSG in HeLa cells.
Figure 8. (a) Analysis of intracellular GSH content after 24 h exposure of HeLa to different concentration of compound 3a. (b) Quantification of the ratio of GSH/GSSG in HeLa cells.
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Figure 9. Statistical graph of differential gene expression. (a) Heat map. (b) Volcano map of differential gene expression. (c) KEGG pathway of differentially expressed genes. (d) GO enrichment analysis of differentially expressed genes.
Figure 9. Statistical graph of differential gene expression. (a) Heat map. (b) Volcano map of differential gene expression. (c) KEGG pathway of differentially expressed genes. (d) GO enrichment analysis of differentially expressed genes.
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Figure 10. (a) The expressions of PARP, Caspase-3, Caspase-7, Bcl-2 and Bax, and GPX4 were determined using western blotting assay. β-actin was used as a reference control. (b) Quantitative analysis of protein expression of PARP, Caspase-3, Caspase-7, Bcl-2 and Bax, GPX4.
Figure 10. (a) The expressions of PARP, Caspase-3, Caspase-7, Bcl-2 and Bax, and GPX4 were determined using western blotting assay. β-actin was used as a reference control. (b) Quantitative analysis of protein expression of PARP, Caspase-3, Caspase-7, Bcl-2 and Bax, GPX4.
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Figure 11. The mechanism of compound 3a inducing cell apoptosis.
Figure 11. The mechanism of compound 3a inducing cell apoptosis.
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Table
Table 1. IC50 (μM) values of 3a–3f toward the selected cancer cells for 48 h.
Table 1. IC50 (μM) values of 3a–3f toward the selected cancer cells for 48 h.
CompoundSGC-7901BEL-7402B16A549HeLaLO2
3a48.4 ± 1.732.4 ± 3.647.4 ± 2.339.5 ± 8.511.4 ± 0.252.4 ± 3.0
3b44.9 ± 5.939.9 ± 4.544.4 ± 5.717.7 ± 2.024.0 ± 0.832.4 ± 7.4
3c43.5 ± 3.8>10056.7 ± 4.545.3 ± 3.438.0 ± 6.474.2 ± 5.5
3d32.1 ± 4.426.4 ± 3.239.1 ± 4.726.9 ± 1.523.2 ± 0.8978.7 ± 4.4
3e73.1 ± 5.6>10043.4 ± 3.621.2±1.126.6 ± 1.536.7 ± 3.0
3f69.2 ± 13.341.6 ± 2.348.3 ± 1.232.7 ± 1.745.5 ± 2.171.7 ± 2.6
GA75.9 ± 10.845.9 ± 3.657.6 ± 5.861.1 ± 12.562.9 ± 3.487.5 ± 5.5
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MDPI and ACS Style

Chen, J.; Xu, Y.; Yang, Y.; Yao, X.; Fu, Y.; Wang, Y.; Liu, Y.; Wang, X. Evaluation of the Anticancer Activity and Mechanism Studies of Glycyrrhetic Acid Derivatives toward HeLa Cells. Molecules 2023, 28, 3164. https://doi.org/10.3390/molecules28073164

AMA Style

Chen J, Xu Y, Yang Y, Yao X, Fu Y, Wang Y, Liu Y, Wang X. Evaluation of the Anticancer Activity and Mechanism Studies of Glycyrrhetic Acid Derivatives toward HeLa Cells. Molecules. 2023; 28(7):3164. https://doi.org/10.3390/molecules28073164

Chicago/Turabian Style

Chen, Ju, Yunran Xu, Yan Yang, Xin Yao, Yuan Fu, Yi Wang, Yunjun Liu, and Xiuzhen Wang. 2023. "Evaluation of the Anticancer Activity and Mechanism Studies of Glycyrrhetic Acid Derivatives toward HeLa Cells" Molecules 28, no. 7: 3164. https://doi.org/10.3390/molecules28073164

APA Style

Chen, J., Xu, Y., Yang, Y., Yao, X., Fu, Y., Wang, Y., Liu, Y., & Wang, X. (2023). Evaluation of the Anticancer Activity and Mechanism Studies of Glycyrrhetic Acid Derivatives toward HeLa Cells. Molecules, 28(7), 3164. https://doi.org/10.3390/molecules28073164

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