SH003 selectively induces p73‑dependent apoptosis in triple‑negative breast cancer cells

Introduction

Triple-negative breast cancer (TNBC) is one of the most common types of malignant tumors in women worldwide and is now the third leading cause of cancer-related mortality (1). TNBC is characterized by the absence of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2) (2). Thus, TNBC patients do not benefit from commonly used anti-estrogen and -herceptin-based therapies (3). In addition, patients with TNBC have been reported to have a poorer survival rate, and recurrence and distant metastases occurs more frequently than in patients with other types of breast cancer (4). Recent studies have revealed that TNBC comprises a heterogeneous group of tumors encompassing several molecular subtypes, such as luminal A, luminal B, HER2-enriched, claudin-low and basal-like tumors (5–7). Approximately 62% of basal-like TNBC and 43% of non-basal-like TNBC exhibit mutations in the tumor suppressor p53 (MTp53). The majority of p53 mutations observed in the tumor are loss-of-function mutations; however, some patients have been shown to exhibit oncogenic gain-of-function mutations. Therefore, targeting p53 may be less effective in TNBC treatment (8). Thus, successful treatment of p53-mutant TNBCs remains challenging. Doxorubicin (DOXO) and cisplatin (CDDP) are common treatment options for TNBC. However, acquired resistance and toxicity against these drugs eventually occurs, preventing effective treatment (9). Thus, novel therapies that overcome drug resistance and toxicity in p53-mutant TNBC cases are urgently required.

p73 is a member of the p53 gene family and has been shown to regulate p53 target genes in p53-deficient cancer cells (10). In contrast to p53, p73 is rarely mutated or lost in cancer (11). p53 deficient cancers are partly resistant to chemotherapy; however, not completely chemo-resistant. As p53 deficient cancers have other types of p53 family members such as p73, they may be able to replace the function of p53 in response to DNA damage (12). Therefore, identifying anticancer agents that can activate p73 may provide a chemotherapeutic approach for treating drug-resistant p53-mutant cancers. Recently, nonhydrolyzable ether analog of RRR-α-tocopherol in combination with DOXO or CDDP has been reported to target p53-mediated genes in a p73-dependent manner, enhancing the apoptosis of TNBC cells (9).

Traditional herbal medicines have recently been revisited for cancer therapy as herbal extracts or mixtures based on traditional medicines have exhibited anticancer effects with no or fewer side effects compared with current anticancer therapeutics, including chemical compounds and targeted antibodies (13). Previous studies have demonstrated the anticancer effects of herbal extracts from Astragalus membranaceus (Am), Angelica gigas (Ag) and Trichosanthes kirilowii Maximowicz (Tk) in different cancer cell types, such as leukemia, hepatocellular carcinoma, colon cancer, non-small cell lung cancer and gastric cancer cells (14–19). Furthermore, extracts from a mixture of Am and Ag have been shown to affect various diseases, including hematological diseases and endocrine disorders (20–22).

The present study demonstrated that SH003 extracted from a herbal mixture (Am, Ag and Tk) exhibited anticancer effects on TNBC via activation of the p73 pathway. Thus, SH003 may be useful for the treatment of TNBC.

Materials and methods

Cell culture and reagents

Established Hs578T, MDA-MB-231, ZR-75-1, MCF7 and T47D human breast cancer cell lines were purchased from the American Type Culture Collection (Manassas, VA, USA). All cell lines were maintained in RPMI-1640 medium (Gibco, Thermo Fisher Scientific Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS; Gibco, Thermo Fisher Scientific Inc.), 100 units of penicillin and 100 μl/ml streptomycin. All cells were cultured in a 5% CO2 incubator at 37°C. SH003 was extracted from Am, Ag or Tk, which were provided by Dr S.G. Ko (College of Korean Medicine, University of Kyung Hee, Seoul, Korea) as previously described (23).

Cell viability and cell death analysis

Cells (2×105 cells per plate) were seeded in a 60-mm plate and treated with various concentrations of SH003 (50, 100 or 200 μg/ml) for 48 h. Cell viability and cell death were assessed using a trypan blue exclusion method. Cell pellet was harvested and resuspend in 1 ml of phosphate-buffered saline (PBS). A total of 10 μl 0.4% trypan blue was gently mixed with 10 μl cell suspension. The mixture was applied to a hemocytometer and the number of trypan blue stained and non-stained cells were counted under a light microscope. The percentage of viable cells was calculated.

Colony formation assay

Cells were seeded at a density of 3×102 cells per well in a 6-well plate and were treated with various concentrations of SH003 (50, 100 or 200 μg/ml) for 24 h. The cells were cultured for 14 days and colonies were fixed with 4% paraformaldehyde and stained with a 0.01% crystal violet. Colony counts were performed manually using a light microscope and images of each plate were obtained.

RNA interference

Cells were transiently transfected with small interfering (si)RNA using the Lipofectamine RNAi MAX reagent (Invitrogen, Thermo Fisher Scientific, Inc., Waltham, MA, USA) according to the manufacturer's protocol. The siRNA sequence for transfection was p73-siRNA, 5′-GCAAUAAUCUCUCGCAGUAUU-3′ and scramble-siRNA, 5′-GGACUCUCGGAUUGUAAGAUU-3′

Western blot analysis

Cell lysates were prepared with radioimmunoprecipitation assay (RIPA) lysis buffer (50 mM Tris-HCl, pH 7.5; 50 mM NaCl, 1 μM EGTA and 1% Triton X-100) containing a protease inhibitor cocktail. Protein concentrations in extracts were determined using a Bradford assay (Bio Rad Laboratories, Inc., Hercules, CA, USA). Total cellular proteins (20 μg) were subjected to 10–15% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred to polyvinylidene difluoride membranes. The membranes were blocked with 5% non-fat dry milk in Tris-buffered saline with Tween-20 (TBST) buffer (20 mM Tris-HCl, pH 7.4, 150 mM NaCl, 0.1% Tween-20) and probed with anti-poly ADP ribose polymerase (PARP; cat. no. 9542; 1:1,000), anti-p73 (cat. no. 14620; 1:1,000), anti-caspase 3 (cat. no. 9661; 1:1000; Cell Signaling Technology, Beverly, MA, USA) or anti-β-actin (cat. no. sc-47778; 1:2,000; Santa Cruz Biotechnology Inc., Dallas, TX, USA) primary antibodies at 4°C overnight. Subsequently, the membranes were washed three times with TBST. Primary antibodies were detected following 2 h incubation at room temperature with a horseradish peroxidase-conjugated anti-mouse (cat. no. 7076; 1:2,000) or anti-rabbit secondary antibody (cat. no. 7074; 1:2,000; Cell Signaling Technology, Danvers, MA, USA). Blots were developed with an enhanced chemiluminescence detection kit (Amersham, Buckinghamshire, UK).

Cell cycle analysis

In total, 3×102 cells harvested by trypsinization were fixed in 1 ml of cold 70% ethanol for 24 h at −20°C. After washing cell pellets with 1 ml PBS, pellets were centrifuged at 300 × g for 5 min, discarded supernatant, resuspended in 1 ml staining solution (50 μg/ml propidium iodide, 50 μg/ml RNase and 0.1% Triton X 100 in citrate buffer, pH 7.8), incubated for 30 min and washed with PBS. Cell cycle distribution was analyzed using a FACSCalibur fluorescence-activated cell sorter and CellQuest version 3.0 software (BD Biosciences, San Jose, CA, USA).

Statistical analysis

SPSS version 22.0 (SPSS, Inc., Chicago, IL, USA) was used to perform statistical analysis. Data are presented as the mean ± standard deviation and multiple comparisons were conducted using one-way analysis of variance followed by Newman-Keuls post-hoc test. P<0.05 was considered to indicate a statistically significant difference.

Results

SH003 selectively inhibits the cell viability of TNBC cells

The viability of two breast cancer cell types, TNBC (Hs578T, MDA-MB-231 and ZR-75-1) and non-TNBC (MCF7 and T47D) was determined following exposure to SH003. Cells were treated with various concentrations (50, 100 and 200 μg/ml) of SH003. A significant decrease in cell viability was observed in TNBC cells (P<0.05 for the 100 μg/ml group and P<0.01 for the 200 μg/ml group compared with the untreated cells) but not in non-TNBC cells (Fig. 1A). MDA-MB-231 cells were further used as the cells showed the most effectively reduced cell viability in a dose-dependent manner. Additionally, colony formation analyses revealed a significant decrease in the number of MDA-MB-231 (TNBC) cells treated with SH003 but not MCF-7 (non-TNBC) cells (Fig. 1B; P<0.005 compared with the untreated cells). These results indicate that SH003 selectively decreases TNBC cell viability.

Figure 1 SH003 selectively inhibits the cell viability of TNBC cells. (A) TNBC cell lines (Hs578T, MDA-MB231 and ZR-75-1) and non-TNBC cell lines (MCF-7 and T47D) were treated with the indicated concentrations of SH003, and their cell numbers were assessed by a trypan blue exclusion assay. Data are presented as the mean ± standard deviation (n=6). *P<0.05 and **P<0.01, compared with the untreated cells. (B) MDA-MB-231 and MCF-7 cells were pre-treated with the indicated concentrations of SH003 for 24 h. After incubation for 15 days, colonies with >50 cells were counted. Data are presented as the mean ± standard deviation (n=3). *P<0.005 compared with the non-treated cells. TNBC, triple-negative breast cancer.

SH003 induces caspase-dependent cell death in TNBC cells

The effect of SH003 on cell death in MDA-MB-231 cells was determined using flow cytometry. A significant increase in the number of cells at the sub-G1 phase was observed following SH003 treatment (50, 100 and 200 μg/ml) (Fig. 2A) (P<0.05 and P<0.01 compared with the untreated cells). Apoptotic cell death and PARP cleavage in response to SH003 treatment were assessed in MDA-MB-231 cells using western blot analysis. The expression levels of cleaved PARP increased significantly in a dose-dependent manner compared with the untreated cells (P<0.05; Fig. 2B). SH003-induced apoptosis after pre-treatment with a pan-caspase inhibitor, Z-VAD was then examined. Pre-treatment with Z-VAD partially decreased the MDA-MB-231 cell death and levels of cleaved PARP induced by SH003 (Fig. 2C; P<0.05 compared with cells treated with SH003 only). Thus, SH003-induced cell death is partially caspase-dependent in TNBC cells.

Figure 2 SH003 induces caspase-dependent cell death in TNBC. (A) MDA-MB-231 cells treated with the indicated concentrations of SH003 for 48 h and analyzed by flow cytometry after staining with propidium iodide. Data are presented as the mean ± standard deviation (n=3). *P<0.05 and **P<0.01, compared with the untreated cells. (B) MDA-MB231 cells were treated with the indicated concentrations of SH003 for 48 h. Cell lysates were analyzed by western blotting using an anti-PARP antibody. The β-actin level was used as a loading control. (C) MDA-MB-231 cells were pretreated with 100 mM Z-VAD, a pan-caspase inhibitor, followed by SH003 (200 μg/ml) for 48 h. Cell death was determined by a trypan blue exclusion assay. Data are presented as the mean ± standard deviation (n=3). *P<0.05, compared with cells treated with SH003 only. TNBC, triple-negative breast cancer; PARP, poly ADP ribose polymerase.

Induction of p73 expression by SH003 leads to apoptosis in TNBC

A previous study indicated that p73 expression may prevent drug resistance and toxicity in p53-mutant TNBC (8). It was demonstrated that SH003 induced p73-mediated apoptosis in p53 mutant MDA-MB-231 cells. p73 expression in MDA-MB-231 cells was observed following treatment with SH003 using western blot analysis. The p73 protein levels in MDA-MB-231 cells treated with SH003 increased in a dose-dependent manner (Fig. 3A). To confirm that MDA-MB-231 cell death induced by SH003 was correlated with p73, the effect of knockdown of endogenous p73 using small interfering RNAs in MDA-MB-231 cells was examined. Cells were transfected with scrambled siRNA or p73 siRNA, followed by treatment with SH003. Transfected p73 siRNA decreased cell death and PARP cleavage compared with scrambled siRNA treatment (Fig. 3B; P<0.05 compared with SH003 single-treated scramble cells). Additionally, cell death was confirmed using flow cytometric analysis. The number of cells in the sub-G1 phase following SH003 treatment was decreased in the p73 siRNA-transfected cell line compared with the scrambled siRNA-transfected cell line (Fig. 3C; P<0.05 compared with SH003 single-treated scramble cells). These results indicated that the induction of p73 expression by SH003 leads to the apoptosis of MDA-MB-231 cells.

Figure 3 Induction of p73 expression by SH003 leads to apoptosis in TNBC. (A) MDA-MB231 cells were treated with the indicated concentrations of SH003 for 48 h. Cell lysates analyzed by western blotting using an anti-p73 antibody. β-actin was used as a loading control. (B) MDA-MB231 cells were transfected with scrambled siRNA or p73 siRNA and then incubated with or without SH003 (200 μg/ml) for 48 h. Cell death was determined by a trypan blue exclusion assay. Data are presented as the mean ± standard deviation (n=3). Cell lysates analyzed by western blotting using anti-p73 and anti-PARP antibodies. β-actin levels were used as loading controls. (C) MDA-MB231 cells were transfected with scrambled siRNA or p73 siRNA, incubated with or without SH003 (200 μg/ml) for 48 h, and then analyzed by flow cytometry after staining with propidium iodide. Data are presented as the mean ± standard deviation (n=2). *P<0.05 compared with SH003-treated scramble cells.

SH003 sensitizes paclitaxel-induced MDA-MB-231 cell death

Paclitaxel (taxane) is a commonly used treatment in conjunction with other anticancer agents for TNBC; however, paclitaxel treatment occasionally fails due to drug resistance. It was demonstrated that SH003 in combination with paclitaxel synergistically increases cell death in TNBC cell compared with individual treatments (Fig. 4A; P<0.05 compared with cells treated with SH003 or paclitaxel only). Western blot analyses indicated that SH003 in combination with paclitaxel increased the levels of cleaved caspase-3 in MDA-MB-231 cells but did not alter p73 expression (Fig. 4B). These results indicate that SH003 in combination with paclitaxel synergistically enhances apoptosis in TNBC cells.

Figure 4 SH003 sensitizes paclitaxel-induced cell death in MDA-MB-231 cells. MDA-MB-231 cells were treated with SH003 (100 μg/ml) alone, paclitaxel (10 μM) alone or a combination of the two for 48 h. (A) Cell death was determined by a trypan blue exclusion assay. Data are presented as the mean ± standard deviation (n=3). *P<0.05 compared with SH003 or paclitaxel single-treated scramble cells. (B) Cell lysates were analyzed by western blotting using anti-p73 and anti-caspase3 antibodies. β-actin was used as a loading control.

Discussion

TNBC accounts for 10–20% of all types of breast cancer (24). TNBC is an aggressive histological subtype with limited treatment conditions and poor prognosis following standard chemotherapy. The anticancer effects of commonly used chemotherapeutic agents, such as paclitaxel, doxorubicin and cisplatin are limited to cure patients with TNBC due to acquired drug resistance and toxicity (9). The present study focused on anticancer therapy for TNBC to overcome resistance against conventional therapies.

The present chemotherapeutic agents for TNBC are DNA-damaging agents (25). In the DNA-damage pathway, tumor suppressor p53 is important in anticancer actions of DNA-damaging agents (26). A recent study reported that regulation of p53-mediated apoptotic signaling occurs in a p73-dependent manner, which results in enhanced apoptosis in p53-deficient TNBC (9). The functional and structural similarities of p53 and p73 have been previously reported (10). It is also known that p73 can replace the function of p53 in response to DNA damage in p53-deficient cancers. p73 is not frequently mutated in cancers and regulates p53 target genes, such as Bax and Noxa in p53-deficient cancers (27,28). The key role of p73 in anti-cancer effects for p53-deficient TNBC was identified.

Identification and development of traditional herbal medicines has increased due to their potential anticancer effects and minimal side effects. This study demonstrated that SH003 inhibited TNBC growth in a dose-dependent manner. Treatment with SH003 resulted in apoptotic cell death as shown by increased PARP cleavage, a caspase-dependent apoptotic marker. In addition, SH003-induced apoptosis was validated after pretreatment with the pan-caspase inhibitor, Z-VAD, as this partially decreased cell death in MDA-MB-231 cells.

Notably, apoptotic cell death induced by SH003 was associated with induction of p73 expression in TNBC. The anticancer effect of SH003 was validated upon siRNA-mediated knockdown of p73. The results showed that knockdown of p73 decreased apoptotic cell death induced by SH003 treatment. In addition, single treatment with paclitaxel did not result in any specific cell death, while SH003 in combination with paclitaxel synergistically increased cell death in TNBC. Therefore, SH003 in combination chemotherapies may aid in overcoming resistance to conventional chemotherapies in TNBC.

The apoptotic cell death induced by SH003 is associated with p73 expression, which indicates that the anticancer effects of SH003 are induced by p73-dependent apoptosis. This study showed that SH003 induced the expression of p73- and caspase-dependent apoptosis. Thus, this study revealed that a traditional herbal medicine, SH003, has a significant anticancer effect via p73-mediated apoptosis in TNBC cells and confirmed p73 as a promising therapeutic target for TNBC.

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Acknowledgments

This study was supported by grants from Basic Science Research Program through the the National Research Foundation of Korea (NRF) grant funded by the Korean government (MEST), Seoul, Republic of Korea (NRF-2013R1A2A2A01067394) to Professor Dong-Hoon Jin, and the Korean Medicine R&D Project of the Ministry of Health and Welfare to Professor Seong-Gyu Ko (B110043).

References