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Introduction

Breast cancer accounts for 25% of all cancer cases around the world. In 2012, breast cancer was reported to cause 15% of all cancer-associated mortality among women (1). Furthermore, cancer metastasis is the major cause of cancer-associated mortality. Metastatic breast cancer is one of the most life-threatening types of cancer in women, with a mortality rate of >400,000 each year worldwide (2). A series of molecular mechanisms are associated with the migration and invasion of breast cancer cells, including the upregulated expression of matrix metalloproteinases, the promotion of the epithelial-to-mesenchymal transition (EMT), and the activation of nuclear factor-κB, cancer-induced angiogenesis, vascular endothelial growth factor, and mammalian target of rapamycin signaling pathways (3,4). However, cancer metastasis is a complex process and a detailed understanding of its mechanism requires further investigation.

B-cell lymphoma/leukemia gene-2 (Bcl-2) is the first proto-oncogene to be demonstrated to function by inhibiting programmed cell death/apoptosis (5). Bcl-2 integrates multiple survival- and death-related signals, which are generated within the cell (5–7). However, the mechanisms underlying the non-apoptotic functions of Bcl-2 remain to be fully elucidated. Previously, Bcl-2 was found to be involved in cancer cell invasion and metastasis (8). At the cellular level, the overexpression of Bcl-2 was reported to increase invasion and migration in glioma (9,10), lung (11) and breast cancer (12,13). In animal models, Kang et al showed that the overexpression of Bcl-2 mediated the metastasis of the MDA-MB-231 human mammary epithelial cell line to the bone (14). Bcl-2 has subsequently been shown to induce cellular metastasis to the lung with in mouse EpH4 mammary epithelial cell line (15). Efforts made to develop chemical inhibitors of BCL-2 have been reported extensively (16). In primary breast cancer, ~75% of cases express elevated levels of Bcl-2, of which 85% are estrogen receptor (ER)-positive and 50% are human epidermal growth factor receptor 2 (HER-2)-positive tumors (17,18). In breast cancer, there appears to be a correlation between a high level of Bcl-2 and a poorer clinical outcome (19,20). The analysis of patient samples has shown that the expression of Bcl-2 in cancer cells was associated with liver metastasis in breast (21) and colorectal (22) cancer. Additionally, upregulation in the expression of Bcl-2 was found during the progression from pre-invasive lesions to invasive carcinoma in lung cancer samples (11). The overexpression of Bcl-extra large (Bcl-XL), another member of the Bcl-2 family, induces invasion and metastasis (lymph node or distal metastasis) in patients with breast cancer (22). This evidence led the present study to focus on the function of Bcl-2 in the invasion and migration of breast cancer.

The EMT is one of the key events in cancer invasion and metastasis. It has been reported that reversing EMT may suppress the metastasis of breast cancer (23). The overexpression of N-cadherin in MCF-7 breast cancer cells also induces cell migration, invasion and metastasis, without altering the endogenous expression or adhesiveness of E-cadherin (24). Furthermore, it was reported that Bcl-2 regulated Twist-targeted genes, including the E-cadherin gene (13,25). The overexpression of Bcl-2 may inhibit the expression of E-cadherin and promote EMT in different types of cell (13,26,27). Therefore, Bcl-2 may be involved directly or indirectly in the transcriptional regulation of EMT.

In the present study, it was shown that the overexpression of the anti-apoptotic protein Bcl-2 increased the migration of BCap37 cells, an ER-negative, HER2-positive human medullary breast cancer cell line (28) and induced cancer metastasis in vivo. The results also indicated that this Bcl-2-induced metastasis may result from the progression of EMT.

Materials and methods

Mice and cell lines

Female Balb/c mice were purchased from Vital River Laboratories, Co., Ltd. (Beijing, China). The BCap37 human breast cancer cell line was purchased from the Cell Bank of the Chinese Scientific Academy (Shanghai, China). The BCap37 cells were cultured in Roswell Park Memorial Institute (RPMI)-1640 medium (cat. no. 31800105; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS; cat. no. 04-0101-1; Biological Industries USA, Inc., Cromwell, CT, USA). The cell culture medium was replaced every 2–3 days, and cells were passaged using 0.25% trypsin-EDTA (cat. no. 25200056; Gibco; Thermo Fisher Scientific, Inc.), once they reached 90% confluence. The cultures were maintained at 37°C, 5% CO2 in a water-jacketed incubator (Thermo Fisher Scientific, Inc.).

Knock down of Bcl-2 in BCap37 cells

The Bcl-2 short hairpin (sh)RNA 5′-CCGGCGTGATGAAGTACATACATTACTCGAGTAATGTATGTACTTCATCACGTTTTTG-3′ (BC-shRNA-Bcl2 #1) or 5′-CCGGGCACACCTGGATCCAGGATAACTCGAGTTATCCTGGATCCAGGTGTGCTTTTTG-3′ (BC-shRNA-Bcl2 #2) sequences were cloned into the pLKO.1-TRC cloning vector. The plasmids were transfected into 293T cells (Cell Bank of the Chinese Academy of Sciences, Beijing, China) using Lipofectamine 2000 (Invitrogen; Thermo Fisher Scientific, Inc.) and the supernatant containing lentiviral plasmids was collected to infect BCap37 cells. RNA silencing was analyzed using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and western blot analyses.

Vector construction, lentivirus production and cell transfection

A Bcl-2 overexpression vector was constructed by introducing the Bcl-2 coding sequence into the pCDH-CMV-EF1-Puro vector (pLVX-Bcl2). The Bcl-2 cDNA sequence was amplified from BCap37 cDNA using the forward 5′-ATAGCTAGCGCCACCATGGCGCACGCTGGGAGAACA-3′ and reverse 5′-ATAGCGGCCGCTCACTTGTGGCCCAGATAGGCAC-3′ primers (the thermocycling steps are provided in Table I). The pLVX-Bcl2 vector was mixed with the psPAX2 and PMD2.G packaging plasmids, and cotransfected into the 293T cells using Lipofectamine 2000 (Invitrogen; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. The virus particles were harvested 48 h following transfection. The BCap37 cells were infected with the harvested recombinant lentivirus and were isolated using puromycin to establish stable cell lines constitutively overexpressing Bcl-2 (BC-Bcl2). BCap37 cells transfected with an empty lentiviral vector served as a control (BC-Mock).

Table I. Thermocycling steps for B-cell lymphoma 2 gene amplification.

Table I.

Thermocycling steps for B-cell lymphoma 2 gene amplification.

98°C	2 min (Ramp rate: 4.4°C/sec)	1 cycle
98°C	10 sec (Ramp rate: 4.4°C/sec)	35 cycles
55°C	15 sec (Ramp rate: 2.2°C/sec)
72°C	15 sec (Ramp rate: 2.2°C/sec)
72°C	10 min (Ramp rate: 2.2°C/sec)	1 cycle
4°C	1 min (Ramp rate: 2.2°C/sec)	1 cycle

RNA isolation and RT-qPCR analysis

Total RNA was isolated using RNAiso Plus (Takara Biotechnology Co., Ltd., Dalian, China) and transcribed into cDNA using the PrimeScript RT Reagent kit (Takara Biotechnology Co., Ltd.). The RT-qPCR was performed using an ABI 7500 FAST Real-Time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.) and a SYBR Green PCR kit (cat. no. RR420A, Takara Biotechnology Co., Ltd.). The thermocycling steps were according to the manufacturer's instruction and the qPCR primers were shown in Table II. The relative expression levels of mRNA were quantified with the 2−ΔΔCq method (29), following normalization using GAPDH endogenous reference.

Table II. Primers used for reverse transcription-quantitative polymerase chain reaction.

Table II.

Primers used for reverse transcription-quantitative polymerase chain reaction.

Primer	Sequence (5′-3′)
BCL-2-F	GTCTTCGCTGCGGAGATCAT
BCL-2-R	CATTCCGATATACGCTGGGAC
GAPDH-F	GGAGCGAGATCCCTCCAAAAT
GAPDH-R	GGCTGTTGTCATACTTCTCATGG

Wound-healing assays

Following transfection, the cells were grown to 100% confluence in six-well plates. A micropipette tip was used to introduce a cross wound, and wound healing was observed 48 h later. Images were captured under phase-contrast microscopy (Olympus, Tokyo, Japan), immediately or 48 h following wounding.

Cell proliferation assay

Cell proliferation was analyzed using the Cell Counting kit-8 assay (CCK8; Dojindo Molecular Technologies, Inc., Kumamoto, Japan). The BCap37, BC-shRNA-NC, BC-shRNA-Bcl2, BC-Mock or BC-Bcl2 cells were seeded into 96-well plates at a density of 1,000 cells per well and the growth rates were subsequently evaluated. Each assay was performed in triplicate.

Cell migration and invasion assay

The cell migration and invasion assays were performed using Transwell chambers (EMD Millipore, Boston, MA, USA). For the invasion assay, the inserts were coated with Matrigel (BD Biosciences, Franklin Lakes, NJ, USA) on the upper surface. Following transfection, 6×104 BCap37 cells were suspended in 0.2 ml serum-free medium and added to the inserts. Subsequently, 0.6 ml RPMI-1640 medium supplemented with 10% FBS was added to the lower compartment, as a chemoattractant. Following incubation at 37°C for 24 h, the cells on the upper surface of the membrane were carefully removed using a cotton swab, and the cells on the lower surface were fixed with 100% methanol and stained with 0.1% crystal violet. Five visual fields (magnification, ×200) of each insert were randomly selected and counted using light microscopy.

Western blot analysis

Cellular proteins were isolated in a protein extraction buffer (Beyotime Institute of Biotechnology, Haimen, China). Equal quantities (40 µg/lane) of proteins were fractionated on 6–10% SDS-PAGE gels and transferred onto polyvinylidene difluoride membranes. The membranes were incubated with anti-Bcl2 (1:1,000 dilution; cat. no. sc-130307), anti-E-cadherin (1:1,000 dilution; cat. no. sc-59780) and anti-vimentin (1:1,000 dilution; cat. no. sc-80975) primary antibodies (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) at 4°C overnight. Then, the blots were incubated for 2 h at room temperature in a 1:10,000 dilution of HRP goat anti-rabbit IgG antibody (cat. no. ab6721; Abcam, Cambridge, UK) after 3 washes with PBST. After extensive washing, antibody detection was accomplished with a sensitive substrate (Immun-Star™ Western C™ kit, 170-5070; Bio-Rad Laboratories, Inc., Hercules, CA, USA). β-actin (1:1,000 dilution; cat. no. ab20272; Abcam) was used for the normalization of protein loading. The image densitometry was performed using Image Lab software (version 5.2.1 Bio-Rad Laboratories).

Examination of tumor growth and metastasis in vivo

To develop human breast xenografts, in vitro grown BCap37, BC-shRNA-C, BC-shRNA-Bcl2, BC-Mock and BC-Bcl2 cells (1×106 cells in 0.2 ml PBS) were implanted into the right flanks of homozygous female nude athymic mice (5–6 weeks old abd weighing 17–21 g). The mice were housed in a temperature-controlled environment with 12 h light and dark cycles and received a standard food and water diet ad libitum. Two perpendicular diameters (width and length) of the mouse tumors were measured three times a week until the animals were sacrificed after 30 days. In addition, a tumor growth curve was drawn based on the tumor volume and the corresponding time (days) post-injection. When the animals were sacrificed, the lungs were harvested and fixed in 10% neutral formalin and embedded in paraffin. 4 µm sections were prepared and stained with hematoxylin and eosin (H&E), followed by examination under a microscope and image capture. The area of metastasis (pixels) of each lung metastasis from different injection groups was calculated using Adobe Photoshop (version CS5; Adobe Systems, Inc., San Jose, CA, USA). Each dot represented the sum of pixels in the lung metastases in the paraffin-embedded section for each mouse (magnification, ×200). Data are representative of at least three separate experiments.

Statistical analysis

Statistical analyses were performed using GraphPad Prism Software (GraphPad Software, Inc., La Jolla, CA, USA). Briefly, data are presented as the mean ± standard error of the mean or mean ± standard deviation of three independent experiments. Two-way analysis of variance (ANOVA) followed by Bonferroni's post-hoc test was used to compare the means of groups affected by two independent factors, whereas a one-way ANOVA followed by Tukey's post-hoc test was used to compare the means of three independent groups. Student's t test was used to compare the means of two independent groups. P<0.05 was considered to indicate a statistically significant difference.

Ethics statement

All animal experiments in the present study were approved by Zhejiang University Animal Care Committee (Hangzhou, China). All animal manipulations were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals (NIH, eighth edition), revised in 2012. The mice were sacrificed using carbon dioxide inhalation. All surgery was performed under sodium pentobarbital anesthesia, and all efforts were made by the attending skilled technician to minimize suffering.

Results

Proliferation of BCap37 cells is not affected by the expression of Bcl-2 in vivo or in vitro

To investigate the effects of Bcl-2 in breast cancer cells in the present study, the expression of Bcl-2 in the BCap37 human breast cancer line was increased or silenced. To increase the expression of Bcl-2, BCap37 cells were transfected either with a CMV promoter-driven Bcl-2 expression vector (BC-Bcl2 1# and BC-Bcl2 2#) or with an empty vector (BC-Mock). Stable cell lines were established and expanded. To inhibit the expression of Bcl-2, the cells were transduced with a lentiviral vector expressing shRNA-Bcl2 (BC-shRNA-Bcl2 1# and BC-shRNA-Bcl2 2#) or with an empty vector (BC-shRNA-NC). The expression level of Bcl-2 in the different cell lines was verified by RT-qPCR and western blot analyses. Bcl-2 was expressed at high levels in the BC-Bcl2 cells, compared with its expression in the BC-Mock cells (Fig. 1A and B). Furthermore, Bcl-2 was effectively silenced in the BC-shRNA-Bcl2 cells, when compared with its level in the BC-shRNA-NC cells. BC-Bcl2 2# and BC-shRNA-Bcl2 1# were selected for the following experiments.

Figure 1. Proliferation of BCap37 cells is not affected by the expression of Bcl-2 in vivo or in vitro. Results of reverse transcription-quantitative polymerase chain reaction (left) and western blot (right) analyses showed that (A) Bcl-2 was expressed at high levels in BC-Bcl2 cells, compared with its levels in BC-Mock cells, and (B) Bcl-2 was effectively silenced in the BC-shRNA-Bcl2 cells, compared with the BC-shRNA-NC cells. Protein levels were quantitated by densitometry. (C) CCK8 assay revealed no statistically significant difference in relative cellular viability of BCap37 cells upon Bcl-2 overexpression or silencing, compared with the control. (D) Tumor growth was not affected by Bcl-2 in BCap37 tumor xenografts. Nude athymic mice were implanted with BCap37, BC-shRNA-NC, BC-shRNA-Bcl2, BC-Mock, and BC-Bcl2, respectively (n=5 for each group). The tumor growth curves in each group are shown. The data are presented as the mean ± standard deviation of three independent experiments. *P<0.05, **P<0.01, ***P<0.001. BC, BCap37 cell; Bcl-2, B-cell lymphoma 2; shRNA, short hairpin RNA; NC, negative control; CCK8, Cell Counting kit-8; n.s., not significant.

To examine the effect of Bcl-2 on the proliferation of BCap37 cells in vitro, the growth rate of BCap37 cells was compared following varying of the expression of Bcl-2. Using the CCK8 assay, no significant differences were observed in the growth rates of the BCap37, BC-Mock, BC-Bcl2, BC-shRNA-NC or BC-shRNA-Bcl2 cells (Fig. 1C).

Subsequently, to assess the effect of Bcl-2 on the proliferation kinetics of BCap37 cells in vivo, the above-mentioned cells were implanted into the right flanks of homozygous nude athymic mice. The tumor volumes following implantation of the different cells were measured every 3 days. After 30 days, when the animals were sacrificed, the mean tumor volumes in the BCap37, BC-Mock, BC-Bcl2, BC-shRNA-NC and BC-shRNA-Bcl2 groups were similar at ~2,059.7±311.1, 2,048.3±290.6, 1,855.5±447.4, 1,898.3±277.2 and 1,806.5±355.1 mm3, respectively (n=5 for each group, Fig. 1D). There were no significant statistical differences among tumor volumes for the different cell groups. In conclusion, the proliferation of BCap37 cells was not affected by the expression of Bcl-2, neither in vitro nor in vivo.

Bcl-2-overexpressing BCap37 cells exhibit a higher migratory and invasive capacity, compared with control cells in vitro

Subsequently, the present study examined whether Bcl-2 affected the migration and invasion capacity of BCap37 cells. Using a wound-healing assay, it was observed that the inhibition of Bcl-2 in BCap37 cells was associated with the inhibition of wound closure, compared with that in the control. Additionally, the overexpression of Bcl-2 in BCap37 cells accelerated wound closure (Fig. 2A and B). A migration chamber assay was used to verify the role of Bcl-2 in cell motility. Bcl-2 significantly promoted the migration of BCap37 cells, whereas the knockdown of Bcl-2 in BCap37 cells inhibited their migration (Fig. 2C upper panel, and D). The invasion chamber assay showed that Bcl-2 increased the invasive capacity of the BCap37 cells. Taken together, these results suggested that Bcl-2-overexpressing BCap37 cells exhibit a higher migratory and invasive capacity, compared with control cells in vitro.

Figure 2. Bcl-2-overexpressing BCap37 cells exhibit a higher migratory and invasive capacity, compared with control cells in vitro. (A) Representative micrographs (magnification, ×100) and results of (B) wound-healing assay in cells expressing BC-shRNA-NC, BC-shRNA-Bcl2, BC-Mock and BC-Bcl2, performed with a 48-h recovery period. Relative migration was calculated as follows: (Cell covered areas (48 h)/Cell covered areas (0 h)). (C) Representative micrographs of Transwell (D) migration and (E) invasion assays (magnification, ×200). Bcl-2 enhanced the migratory and invasive capacity of BCap37 cells in vitro. The data are presented as the mean ± standard deviation of three independent experiments. **P<0.01, ***P<0.001. BC, BCap37 cell; Bcl-2, B-cell lymphoma 2; shRNA, short hairpin RNA; NC, negative control.

Bcl-2 induces lung metastasis of BCap37 cells in vivo

To investigate the effect of Bcl-2 on the kinetics of metastasis of BCap37 cells in vivo, BCap37, BC-Mock, BC-Bcl2, BC-shRNA-NC or BC-shRNA-Bcl2 cells were implanted into the right flanks of homozygous nude athymic mice. Following sacrifice of the animals 30 days post-implantation, the lungs were harvested and stained with H&E. As shown in Fig. 3A and B, the overexpression of Bcl-2 significantly induced the migration of BCap37 cells to the lung. Therefore, Bcl-2 induced the metastasis of BCap37 cells in vivo.

Figure 3. Bcl-2 induces the metastasis of BCap37 cells to the lung in vivo. BCap37, BC-Mock BC-Bcl2, BC-shRNA-NC or BC-shRNA-Bcl2 cells were implanted into the right flanks of homozygous nude athymic mice (n=5 for each group). (A) Representative micrographs (magnification, ×200) and (B) results of histopathological analyses of lung tissues from each group, 30 days post-implantation. ***P<0.001. BC, BCap37 cell; Bcl-2, B-cell lymphoma 2; shRNA, short hairpin RNA; NC, negative control.

Overexpression of Bcl-2 in BCap37 cells induces the progression of EMT

To investigate the effect of Bcl-2 on the progression of EMT, a western blot assay was used to detect the protein levels of EMT markers in cells expressing BC-Mock BC-Bcl2, BC-shRNA-NC or BC-shRNA-Bcl2. The western blot results showed that the overexpression of Bcl-2 inhibited the expression of E-cadherin (an epithelial marker), but increased the levels of N-cadherin and vimentin (mesenchymal markers). In addition, the inhibition of Bcl-2 led to an increase in the expression of E-cadherin, but inhibited the expression of N-cadherin and vimentin (Fig. 4). These results are in agreement with previous reports (18,21), suggesting that the overexpression of Bcl-2 increases breast cancer invasion and metastasis by inducing EMT.

Figure 4. Overexpression of Bcl-2 in BCap37 cells induces the progression of epithelial-to-mesenchymal transition. Western blot assay of cells expressing BC-Mock BC-Bcl2, BC-shRNA-NC or BC-shRNA-Bcl2. Quantification showed that the overexpression of Bcl-2 inhibited the expression of E-cadherin, but increased the levels of N-cadherin and vimentin. The inhibition of Bcl-2 increased the expression of E-cadherin, but inhibited that of N-cadherin and vimentin. Protein levels were quantified by densitometry. BC, BCap37 cell; Bcl-2, B-cell lymphoma 2; shRNA, short hairpin RNA; NC, negative control.

Discussion

Bcl-2 is known as the first proto-oncogene by inhibiting apoptosis, however, the role of Bcl-2 in breast cancer migration and metastasis remains to be fully elucidated. In the present study, it was first found that the proliferation of BCap37 cells was not affected by the expression of Bcl-2, neither in vitro nor in vivo. It has been reported that the knockdown of Bcl-2 has no anti-proliferative effects on colorectal cancer cells (30). Presumably, this may be due to the antagonistic effect of other members of the Bcl-2 family, of which there are several members and a number of which have an anti-proliferative function, with others having the opposite effect. For example, Bcl-2-associated X factor can have negative effects on the anti-apoptotic function of Bcl-2 by forming two dimers with Bcl-2 (31). The present study found that Bcl-2 promoted the migration and metastasis of BCap37 cells in vitro and Bcl-2-overexpressing BCap37 cells were more likely to transfer to the lungs in mice. In line with previous findings, the present study showed the ability of Bcl-2 to regulate cancer invasion and metastasis, and is the first, to the best of our knowledge, to report its function specifically in breast cancer. EMT is one of the key and common events occur in the early age of cancer development. In the present study, it was observed that Bcl-2 induced EMT progression in BCap37 cells, indicating the early and extensive involvement of Bcl-2 in regulating cancer invasion.

As Bcl-2 is vital in tumorigenesis and neoplastic progression, it may be a promising candidate for anticancer therapy. Previous findings confirmed that Bcl-2 offers potential as a prospective drug target. Several small molecular inhibitors of Bcl-2, including ABT-737 and ABT-199, have been investigated extensively (16,32). ABT-737, designed to neutralize the prosurvival proteins BCL-2, BCL-XL and BCL-W, was reported to improve anti-estrogen tamoxifen susceptibility in the treatment of ER-positive breast cancer and triple negative breast tumor xenografts (18,33,34). In addition, it has been reported that herceptin-resistant breast cancer cells show increased sensitivity to ABT-737, suggesting that ABT-737 offers potential as a therapeutic agent (35). ABT-199 (venetoclax), a potent Bcl-2-selective inhibitor previously approved by the Food and Drug Administration for the treatment of chronic lymphocytic leukemia, was reported to be effective in breast cancer treatment, with satisfactory safety and efficacy (36,37). The combination of Bcl-2/Bcl-xl inhibitor ABT-263/ABT-199 with cyclin-dependent kinase 7 inhibitor thz1 can further promote anti-proliferation and induce apoptosis in human triple-negative breast tumor cells (38), showing the compatibility of Bcl-2 chemical inhibitors with other chemotherapeutic drugs.

In conclusion, the present study comprehensively investigated the effect of Bcl-2 on the motility of the BCap37 cell line. It was found that Bcl-2 did not affect the proliferation of BCap37 cells, but promoted cell invasion in vitro and in vivo. In addition, a lung metastasis mouse model of breast cancer was developed, which may be used to evaluate the effectiveness of certain novel medications for metastatic breast cancer in further investigations. For example, one first-in-class CDK4/6 inhibitor, palbociclib, was approved for the treatment of postmenopausal women with ER(+), HER2(−) advanced breast cancer in combination with letrozole, and achieved a good outcome (39–41). In addition, utidelone, an analog of epothilone, has been tested in a phase II trial as a monotherapy or in combination with capecitabine in patients with heavily pre-treated metastatic breast cancer, and the results showed marked advantages of this novel medication with higher efficacy and tolerability (42). The mouse model established in the present study may be used by others to assess these novel agents in vivo. Upon implantation of breast cancer cells and successful model establishment, these agents can be transferred into the body by intravenous injection to determine their effect on tumor growth featured by the number and size of lung metastases. In addition, the combination of agents and cancer cell lines can vary according to the investigation design. For example, as a supplement, the MCF-7 cell line, which expresses ERs, but not HER2, may be used in the model to assess the effect of palbociclib mentioned above. However, the molecular mechanisms underlying the different effects of Bcl-2 on proliferation, migration and invasion require further investigation.

Acknowledgements

The authors would like to thank Professor Youfa Zhu, Ms Yanwei Li and Ms Li Liu of the Public Platform of Zhejiang University of Medicine, for providing technical support for the flow cytometry and immunohistochemical assays.

Funding

No funding was received.

Availability of data and materials

The analyzed data sets generated during the study are available from the corresponding author, on reasonable request.

Authors' contributions

PF conceived and designed the experiments. CD performed the majority of the experiments, including the in vivo work, the and in vitro migration and invasion assays, and contributed to the western blotting. XZ, MY and KL performed the CCK-8 assay and analyzed the majority of the data. JW, LC and SW performed RT-qPCR and helped analyze the HE staining.

Ethics approval and consent to participate

The present study was approved by the Zhejiang University Animal Care Committee (Hangzhou, China). All animal manipulations were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals (8th edition), revised in 2012.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References