Metformin Inhibits Growth of Breast Cancer Cell T47 through Decreasing Expression of Protein P53, BCL2 and Cyclin D1

Irma Yanti Rangkuti, P. Hasibuan, T. Widyawati, Y. Siregar
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引用次数: 1

Abstract

Breast cancer is a disease that afflicts women only 0.5 to 1 % are male breast cancers.Breast cancer has several variants and requires a different therapeutic approach, and until now the therapy has not been satisfactory due to the emergence of resistance. Metformin as the main choice drug type 2 diabetes mellitus which is known to have a cytotoxic effect for breast cancer. This study aimed to analyze metformin cytotoxic mechanisms covering the cell cycle , apoptosis, expression of p53, bcl-2 and cyclin D1 T47D cells which exposed to metformin HCl. The study was conducted invitro on T47D breast cancer cells which exposed to metformin concentrations of 1738.2 µg / mL and 3476.4 µg / mL and doxorubicin concentrations of 0.1µg / mL and 0.2µg / mL for 24 hours. Cell cycle testing and apoptosis using the flowsitometry method and expression test of p53 protein, bcl-2 dancycline D1 in T47D cells with immunocytochemistry. Data was analyzed by one way Anova with Bonferroni's advanced test. The results showed that metformin inhibited the G0-G1 phase of the T47D cell cycle, triggered T47D cell apoptosis, significantly reduced p53, bcl-2 and cyclin D1 protein expression (p <0.05). Conclusion of the study, metformin inhibits T47D cells through inhibition of the cell cycle G0-G1 phase, reducing protein expression p53, bcl-2 and cyclin D1.
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二甲双胍通过降低P53、BCL2和Cyclin D1蛋白的表达抑制乳腺癌细胞T47的生长
乳腺癌是一种折磨女性的疾病,只有0.5%到1%是男性乳腺癌。乳腺癌有多种变体,需要不同的治疗方法,由于耐药性的出现,到目前为止,这种治疗方法并不令人满意。二甲双胍是治疗2型糖尿病的主要药物已知它对乳腺癌有细胞毒性作用。本研究旨在分析二甲双胍对暴露于二甲双胍HCl的T47D细胞的细胞周期、凋亡、p53、bcl-2和cyclin D1表达的影响机制。本研究对暴露于二甲双胍浓度为1738.2µg / mL和3476.4µg / mL,阿霉素浓度为0.1µg / mL和0.2µg / mL的T47D乳腺癌细胞进行了体外研究。流式法检测T47D细胞周期和凋亡,免疫细胞化学检测p53蛋白、bcl-2舞素D1的表达。数据分析采用Bonferroni先进检验的单因素方差分析。结果显示,二甲双胍抑制T47D细胞周期G0-G1期,触发T47D细胞凋亡,显著降低p53、bcl-2和cyclin D1蛋白表达(p <0.05)。本研究结论:二甲双胍通过抑制细胞周期G0-G1期,降低p53、bcl-2和cyclin D1的蛋白表达来抑制T47D细胞。
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