Combined treatment of glibenclamide and CoCl2 decreases MMP9 expression and inhibits growth in highly metastatic breast cancer.

BACKGROUND: To observe the influence of combination treatment with glibenclamide and CoCl(2) on the growth and invasiveness of TA2 breast cancer, and to detect the protein and mRNA expression of MMP9.
METHODS: 50 adult female TA2 mice were randomly divided into 5 groups including DMSO control, CoCl(2), glibenclamide, CoCl(2) + glibenclamide and paclitaxel. All of these mice were inoculated with TA2 spontaneous breast cancer cells in the left groin. Nine days after inoculation the tumor could be palpated. Different treatments for each group were then subcutaneously administered near the tumors on the 9th and 14th days after injection. Tumor size was measured to determine the growth curve. All mice were sacrificed on the 18th day after initial inoculation and tumor tissues were collected. Some fresh tissues without necrosis were stored at -80°C for mRNA detection and the other tumor tissue was fixed with 10% formalin for H&E and immunohistochemical staining.
RESULTS: The growth rate of tumor cells in the CoCl(2) + glibenclamide group was lower than that seen in the other groups. On the 14th day, the average volume of tumor in the CoCl(2) + glibenclamide group was the lowest and the difference has statistical significance (P < 0.05), while the differences among the CoCl(2), glibenclamide and paclitaxel had no statistical significance. The mean percentage of cells expressing MMP9 and PCNA was the lowest in the CoCl(2) + glibenclamide group (P < 0.05). MMP9 mRNA expression paralleled MMP9 protein expression in these groups (P < 0.05).
CONCLUSIONS: Combined treatment with glibenclamide and CoCl(2) inhibits TA2 spontaneous breast cancer growth and invasiveness with effects similar to paclitaxel.

Background

Surgery accompanied with radiotherapy and chemotherapy is the most successful treatment strategy for breast cancer. However, 40% of patients die of advanced breast cancer recurrence and metastasis [1]. TA2 mouse strains were bred by the Animal Center of Tianjin Medical University twenty years ago. TA2 mice have a high incidence of spontaneous breast cancer without chemical stimulus. The morbidity of breast cancer in multiparous TA2 mice reaches 84.1% and the average time it takes for tumor initiation and development is 280 days [2]. TA2 spontaneous breast cancer tumor cells show high metastatic ability and the rate of lung metastasis reaches more than 80% [2]. When injecting TA2 breast cancer tumor cells into normal TA2 mice, 1 × 105 cells for each mouse can form a palpable tumor 9 days after injection.

Matrix metalloproteinase (MMPs) are very important in the processes of tumor invasion and metastasis through their degradation of the extracellular matrix (ECM) [3,4]. There are many members of the MMP family. MMPs play an important role in the tissue remodeling associated with various physiological and pathological processes such as morphogenesis, angiogenesis, tissue repair and metastasis. MMP2 and MMP9 are thought to be important in metastasis [5]. Previous studies in our lab have confirmed that there is high MMP9 expression in TA2 spontaneous breast cancer.

During tumor development, nutrients and oxygen are important for the tumor cells. Hypoxia is known to play an important role in tumor growth and progression. Cells undergo a variety of biological responses when placed in hypoxic conditions and cancer cells have adapted to the hypoxic microenvironment [6]. Tumor hypoxia is associated with poor prognosis and resistance to radiation therapy [7]. Cobalt chloride (CoCl2) has been widely used to mimic hypoxia in cell culture, and it is known to activate signaling by stabilizing the hypoxia-inducible transcription factor 1α (HIF1α) [8,9]. Cobalt chloride (CoCl2) has been widely used as a hypoxia mimic to treat aplastic anemia and renal anemia and induce fibroblasts and epithelial cancer cells to generate their own red blood cells. Glibenclamide is an antidiabetic drug in a class of medications known as sulfonylureas. Glibenclamide treatment results in increased intracellular calcium in beta cells and stimulated insulin release and subsequent decrease in blood glucose level by inhibiting the sulfonylurea receptor 1, the regulatory subunit of the ATP-sensitive potassium channels in pancreatic beta cells [10]. Research shows that glibenclamide improves outcome in animal stroke models by preventing brain swelling and enhancing neuroprotection [11]. A retrospective study showed that glibenclamide has been used in the treatment of type 2 diabetes [12]. Paclitaxel is a first-line chemotherapeutic agent that exerts its effect in the treatment of epithelial ovarian cancer by stabilizing microtubules, inducing cell cycle arrest in the G2-M phase [13], and activating proapoptotic signaling [14,15]. Here, CoCl2 and glibenclamide were used together to inhibit the oxygen and nutrition supply of TA2 breast cancer cells in order to study their combined effects on tumor growth and invasiveness.

Methods

Drugs and animals

CoCl2, Glibenclamide and paclitaxel were purchased from Sigma. CoCl2 was dissolved in ddH2O; Glibenclamide and paclitaxel were dissolved in DMSO. TA2 inbred animals that were clean, white, and 6–8 weeks old were obtained from the Animal Centre of Tianjin Medical University. These mice were bred under SPF. This study was approved by the Animal Welfare Committee of Tianjin Medical University.

Drug experiments in TA2 mice

Fifty TA2 were randomly divided into five groups including DMSO control, CoCl2, glibenclamide, CoCl2 + glibenclamide and paclitaxel with 10 mice for each group. All mice were injected with 1 × 105 TA2 spontaneous breast cancer cells into the lower left groin. Nine days after injection, tumor mass was palpable in the groin of all mice. On the 9th and 14th days after injection, DMSO (0.2 ml), CoCl2 (0.2 ml, 7.76 mg/ml), glibenclamide (0.2 ml, 1.25 mg/ml), CoCl2 (0.2 ml, 7.76 mg/ml) + glibenclamide (0.2 ml, 1.25 mg/ml) and paclitaxel (0.2 ml, 1 μM) were administered subcutaneously to the mice in different groups. The length and width of the tumors were measured using a caliper every other day. The tumor size was calculated according to the following formula: Tumor volume (mm3) = (length × width2)/2. Tumor growth curves were drawn based on tumor size. All TA2 mice were sacrificed on the 18th day after injection of the cells and the tumor masses were removed. Parts of the tumor without necrosis were collected and stored at −80°C and the remainder of the tumors were fixed with 10% formalin and embedded in paraffin for H&E and immunohistochemical staining.

Immunohistochemical staining

Four μm thick paraffin-embedded tissue sections were cut and stained immunohistochemically. The sections were deparaffinized with xylene and rehydraded through graded alcohols. Endogenous peroxidase was blocked with 3% hydrogen peroxide in 50% methanol at room temperature for 10 min. The primary antibodies were diluted to 1:100. The tissue sections were heated in a microwave oven in citrate buffer for about 20 min. The slides were incubated with primary antibodies MMP9 (goat polyclonal, Santa Cruz, sc-6840,1:100) and PCNA (goat polyclonal, Santa Cruz, sc-9857,1:100) overnight at 4°C, washed with PBS, and incubated with the biotinylated secondary antibody and preformed avidin-biotinylated peroxidase complex. The color was developed with DAB. Finally, all of the sections were counterstained with hematoxylin. Human breast cancer was used as a positive control and PBS was used in place of primary antibody to serve as a negative control.

Real-time PCR to detect MMP9 mRNA expression levels

Total RNA from the fresh TA2 tumor samples was extracted with Trizol reagent according to the manufacturer’s instructions. The integrity and purity of isolated RNA were confirmed with 1% agarose gel electrophoresis and OD260/OD280 ratio. Complementary DNA (cDNA) was synthesized and amplified from total RNA using the Access real time PCR system (TaKaRa One Step RNA PCR Kit). The primer sequences used in the reaction are listed in Additional file 1: Table S1. The resultant cDNA products of MMP9 and β-actin were 86 and 174 base pairs, respectively. The products of RT PCR were purified with TaKaRa Agarose Gel DNA Purification Kit Ver.2.0. Real time PCR products were analyzed with the Gene AMP PCR System 5700 Sequence Detector. The size of the real-time PCR products was validated with 1.5% agarose gel electrophoresis. The CT value (the cycle number at which the fluorescence crosses the threshold) was determined and the formula 2^(−ΔΔCT) was used to determine the relative quantity of the amplified fragment, where ΔΔCT = ΔCT MMP9-ΔCT β-actin was defined as the relative quantity of the amplified fragment. Every sample was tested in triplicate and the mean value was used.

Immunohistochemical staining to determine the mean percentage of cells positively stained for MMP9 and PCNA

When stained for MMP9 and PCNA, tumor cells with brown cytoplasm were considered positive. We observed 10 fields per section at 400× magnification, and the mean percentage of positively stained cells was used to determine the expression of the proteins in a section. All counts were performed blindly for at least 3 randomly chosen sections from each mouse.

Statistical analysis

Statistical software SPSS 10.0 (Chicago, Illinois) was used in the analysis. A P value less than 0.05 was considered statistically significant. Differences among groups were assessed using the ANOVA test, and the LSD test was used to compare the differences in MMP-9 (protein and mRNA) and PCNA expression among the different groups.

Results

Combined CoCl2 and glibenclamide treatment influences tumor growth in TA2 mice inoculated with breast cancer cells

The average growth rate of tumor in the mice that received combined treatment with CoCl2 + glibenclamide was obviously inhibited compared to the other groups according to the average tumor size that was measured every other day (Figure 1). All the mice were sacrificed 18 days after the initial inoculation and the tumors were removed. The average tumor volume in the CoCl2 + glibenclamide group was significantly reduced when compared with the other groups (Figure 1), and the differences among these groups had statistical significance (F = 489.5 P = 0.0098).

Figure 1

The growth curve of injected TA2 breast cancer cells in the control and treatment groups.

Morphologic tumor changes in the treatment and control groups

Immediately following sacrifice, breast cancer tissue samples were carefully collected. In the DMSO group, tumor cells invaded the surrounding normal tissue. As shown in Figure 2A, there were large areas of necrosis in tumor tissues from the paclitaxel and CoCl2 + glibenclamide groups, while a small amount of necrosis was observed in the DMSO (Figure 2A-a), CoCl2 (Black arrow heads, Figure 2A-b) and glibenclamide groups (Black arrow heads, Figure 2A-c). Moreover, numerous tumor cells in the CoCl2 + glibenclamide group displayed cell degeneration as suggested by the presence of vacuoles within the cytoplasm (Black arrow heads, Figure 2A -d).

Figure 2

The differences of morphology, MMP9 and PCNA expression of TA2 breast cancer between the control and treatment groups. A. The morphologic characteristics of TA2 breast cancer in the control and treatment groups (HE staining, ×200). a. DMSO group. b. CoCl2 group. c. Glibenclamide group. d. CoCl2 + glibenclamide group. e. Paclitaxel group. B. Immunohistochemical staining for MMP9 and PCNA in the control and treatment groups (immunohistochemical staining, ×200). a. MMP9 staining of DMSO group. b. MMP9 staining of CoCl2 group. c. MMP9 staining of Glibenclamide group. d. MMP9 staining of CoCl2 + glibenclamide group. e. MMP9 staining of paclitaxel group. f. PCNA staining of DMSO group. g. PCNA staining of CoCl2 group. h. PCNA staining of Glibenclamide group. i. PCNA staining of CoCl2 + glibenclamide group. j. PCNA staining of paclitaxel group.

MMP9 and PCNA protein expression in tumor cells in the control and treatment groups

Both the treatment group and the control group contained tumor cells that stained positively for MMP9 and PCNA. MMP9 protein expression was detected mainly in the cytoplasm of tumor cells while PCNA protein expression was seen in the nucleus. PCNA expression occurred in the nuclei of cells during the DNA synthesis phase of the cell cycle and provides an important marker indicating tumor proliferation. The tumor cells that positively stained for MMP9 were mainly distributed at the edge of normal tissue, especially in the area between tumor tissue and skeletal muscle. In the center of the tumor mass, the percentage of positively stained cells was low. Immunohistochemical results showed statistically significant differences for mean percentage of MMP9 positively stained cells among the treatment groups (P = 0.00687, Figure 2B –a to -e). The CoCl2 + glibenclamide group had the lowest MMP9 expression. Results of immunohistochemical staining for PCNA showed that combined treatment with CoCl2 + glibenclamide inhibits tumor growth by decreasing tumor cell duplication, suggested by the mean percentage of positively stained cells that only reached 52.89% (Figure 2B –f to -j). The differences seen in the percentage of cells expressing PCNA among the treatment groups had statistical significance (P = 0.0348) (Table 1). The results of immnohistochemical staining show that combined treatment with CoCl2 + glibenclamide down-regulates MMP-9 and PCNA expression and inhibits tumor growth and invasiveness.

Table 1

Comparison of the mean percentage of cells staining positive for MMP9 and PCNA among the treatment groups

Group	n	MMP9		PCNA
DMSO	10	0.6312 ± 0.1527		0.9156 ± 0.1022
CoCl2	10	0.6028 ± 0.1337		0.8833 ± 0.1857
glibenclamide,	10	0.5711 ± 0.1637	F = 324.5 P = 0.00687	0.9017 ± 0.1772	F = 187.6 P = 0.0348
CoCl2 + glibenclamide	10	0.2856 ± 0.1234		0.5289 ± 0.1403
paclitaxel	10	0.3451 ± 0.1956		0.6574 ± 0.1945

MMP9 mRNA expression among the treatment groups

After extracting total mRNA from fresh tumor tissues taken from the control and treatment groups the concentrations were determined by UV spectrophotometer. Results of electrophoresis in 1% agarose gel showed that the mRNA had no obvious degradation. After performing real-time PCR the products were separated by 1% agarose gel electrophoresis. The MMP9 product was about 86 bp and the optimal annealing temperature was 64.2°C. Results of real time PCR demonstrated that the mRNA expression of MMP9 in the treatment groups was decreased compared with the control group. This trend follows what was seen with MMP9 protein expression. There was statistical significance for MMP9 (P = 0.021) mRNA levels among the groups (Table 2).

Table 2

Comparison of the mRNA expression of MMP9 among the treatment groups

Group	n	MMP9 mRNA
DMSO	10	1.320 ± 0.0524
CoCl2	10	0.881 ± 0.0723
glibenclamide	10	0.941 ± 0.0948	F = 447.86 P = 0.021
CoCl2 + glibenclamide	10	0.481 ± 0.0685
paclitaxel	10	0.424 ± 0.0517

Discussion

Breast cancer is one of the most common malignancies in women. With morbidity increasing worldwide, breast cancer has become a significant threat to human life [16]. In China, the incidence is now 21 cases per million women [17,18]. Breast cancer survival rates indicate that this cancer is one of the most malignant tumors in major metropolitan areas in China [19]. Surgery accompanied with chemotherapy is currently the main treatment strategy for breast cancer [20].

TA2 mice have a high incidence of spontaneous breast cancer without chemical stimulus. The morbidity of spontaneous breast cancer in parous female TA2 mice is 84.1% within an average of 280 days after birth [21]. Previous studies confirmed that TA2 spontaneous breast cancer is associated with MMTV infection and pregnancy-associated hormones, a combination that induces p53 gene mutation and results in the initiation and development of breast cancer [22]. Here normal TA2 mice injected with TA2 spontaneous breast cancer cells were used to compare the efficacy of combined treatment with CoCl2 + glibenclamide, agents that simultaneously cut off nutrition and oxygen.

Tumor hypoxia is well recognized as a major driving force behind many tumor biological behaviors including growth, metabolism, angiogenesis, metastasis, invasion and apoptosis [23,24]. In some advanced tumors, hypoxia can be used as a tool to decrease tumor growth. Pilati and Guadagni et al. [2,3] reported a type of therapy called hypoxic antiblastic stop-flow perfusion (SFP) that can be used as a treatment option for patients with locally advanced tumors [25,26]. CoCl2 has been used in the treatment of anemia and it is known to activate hypoxic signaling by stabilizing HIF1α. CoCl2 can also activate hypoxia-mediated signaling pathways aberrantly under normoxic conditions by stabilizing cytosolic HIF1α [27]. This type of deviation effects long-term hypoxia because cobalt is a metal ion that is not easily cleared from tumor tissue. Glibenclamide is a drug widely used in clinics for the treatment of type 2-diabetes that specifically blocks KATP channels [28]. Different subtypes of potassium channels have been shown to be involved in normal and malignant cell proliferation [29]. Some of these potassium channels are overexpressed in tumors. Other reports have described the antiproliferative effect of glibenclamide in different neoplastic cell lines through the blocking of the KATP channels [30,31]. Furthermore, Glibenclamide can bind to the sulphonylurea receptor (SUR1), a member of the ATP-binding cassette (ABC) protein superfamily, and block the activity of numerous ABC transporters including the P-gp multidrug transporter involved in anticancer drug resistance [32].

TA2 mice with tumor xenografts were treated with CoCl2 and glibenclamide to study the combined effect of blocking both nutrition and oxygen. Results of our study show that the combined blockage of nutrition and oxygen can effectively inhibit tumor growth, proliferation and invasiveness. PCNA plays an important role in nucleic acid metabolism and functions as an accessory protein in DNA synthesis in the S phase [33]. PCNA can interact with cellular proteins involved in cell cycle regulation and checkpoint control [34]. PCNA immunohistochemical staining confirmed that the mean percentage of positively stained cancer cells was the lowest in the group treated with CoCl2 + glibenclamide compared to the other groups. MMPs play important roles in the invasion and metastasis of tumor cells. MMPs can degrade the extracellular matrix (ECM) and release activated growth factors to promote invasion and metastasis [35]. So far, more than 20 kinds of MMPs have been reported. MMP9 is one of the most important proteases and can degrade collagen IV and most of the components of ECM. It has been reported that there is high expression level and activity of MMP9 in many epithelium-derived malignant tumors including breast cancer [36]. The expression and secretion of MMP9 are regulated by MMP2, another member of the MMP family [37]. Immunohistochemical staining showed that the expression of MMP9 in the control groups was significantly higher than that in the CoCl2 + glibenclamide and paclitaxel groups. Moreover, the tumor cells that stained positive for MMP9 were mainly distributed in the margin between tumor tissue and skeletal muscle. In the center of the tumor masses we observed a low number of positively stained tumor cells. This phenomenon of MMP9 expression at the tumor edge has been called the “infiltration striker” and it facilitates infiltration of the tumor cells through the basement membrane and formation of distant metastases.

Nutrition and oxygen are important for sustaining the growth and development of cancer cells [38]. Poor nutrition and oxygen deficiency will hinder rapid proliferation of tumor cells. Here we describe the effect of combined treatment with CoCl2 and glibenclamide on TA2 breast cancer xenografts that resulted in inhibited growth and invasion. Further studies are needed to investigate the mechanism involved.

Conclusions

Combined treatment with glibenclamide and CoCl2 inhibits TA2 spontaneous breast cancer growth and invasiveness with effects similar to paclitaxel.

Abbreviations

TA2: Tientsin Albino 2; CoCl2: Cobalt chloride; DMSO: Dimethyl sulfoxide; MMPs: Matrix metalloproteinases; ECM: Extracellular matrix; PCNA: Proliferating cell nuclear antigen; HIF1α: Hypoxia inducible factor 1α.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

ZR carried out the animal experiment, participated in the design of the study. LL participated the animal experiment and carried out morphological observation. FF carried out the immunohistochemical staining. LL performed the statistical analysis. YQ carried out the data collection and helped to draft the manuscript. SB carried out the design of the study. All authors read and approved the final manuscript.

Additional file 1: Table S1

Primer sequences for real-time PCR.

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