期刊文献+

二甲双胍联合紫杉醇对人乳腺癌MCF-7细胞增殖抑制作用的研究

Inhibitory effect of Metformin combined with Paclitaxel on the proliferation of human breast cancer MCF-7 cells
在线阅读 下载PDF
导出
摘要 目的探讨二甲双胍联合紫杉醇对人乳腺癌MCF-7细胞增殖的抑制作用。方法对人乳腺癌细胞MCF-7进行体外培养,分别以二甲双胍、紫杉醇、二甲双胍联合紫杉醇进行干预,通过CCK-8试剂盒测定干预48小时对人乳腺癌MCF-7细胞增殖的抑制情况。结果联合组细胞抑制率显著高于紫杉醇组和二甲双胍组(P_均<0.05)。联合组G1期细胞比例和Bax蛋白表达水平均显著高于二甲双胍组和紫杉醇组(P_均<0.05),S期、G2期细胞比例及磷酸化细胞外信号调节激酶、细胞外信号调节激酶、B细胞淋巴瘤/白血病-2蛋白表达水平均显著低于紫杉醇组和二甲双胍组(P_均<0.05)。结论二甲双胍联合紫杉醇可抑制人乳腺癌MCF-7细胞增殖,其机制可能与细胞丝裂原激活蛋白激酶通路调节有关。 Objective To investigate the inhibitory effect of Metformin combined with Paclitaxel on the proliferation of human breast cancer MCF-7 cells. Method Human breast cancer MCF-7 cells was cultured, Metformin, Paclitaxel, Metformin and Paclitaxel were used for intervention. The proliferation inhibition of MCF-7 cells was observed by CCK-8 kit for 48 hours. Result The cell inhibition rate of combined group was significantly higher thin1 that of Paclitaxel group and Metformin group (Pall 〈 0.05). The proportion of G1 cells and Bax protein in combined group were significantly higher than that of Metformin group mid Paclitaxel group (Pall 〈0.05), and the proportion of cells in S phase and G2 phase, the expression level of phosphorylation extracellulaJc signal-regulated kinase (p-ERK), extracel-lular regulated protein (ERK), and B cell lymphoma/leukemia-2 (Bcl-2) proteins were significantly lower than Paclitaxel group and Metformin group (Pall 〈 0.05). Conclusion Metformin combined with Paclitaxel can inhibit the proliferation of human breast cancer MCF-7 cells, and its mechanism may be related to the regulation of mitogen-activation protein kinase pathway.
作者 梁君伟 吕喜英 方志华 LIANG Jun-wei;LYU Xi-ying;FANG Zhi-hua(Department of Oncology,Affiliated Hospital of Chengde Medical College,Hebei,Chengde 067000,China)
出处 《中国医学前沿杂志(电子版)》 2018年第11期70-73,共4页 Chinese Journal of the Frontiers of Medical Science(Electronic Version)
基金 河北省医学科学研究重点课题计划(ZL20140246)
关键词 乳腺肿瘤 MCF-7细胞 二甲双胍 紫杉醇 Breast neoplasms MCF-7 cells Metformin Paclitaxel
作者简介 通讯作者:吕喜英E-mail:79818794@qq.com
  • 相关文献

参考文献17

二级参考文献197

  • 1何静松,林茂芳,蔡真,钱文斌.野生型p53基因蛋白在氨肽酶抑制剂诱导人白血病细胞株K562细胞凋亡的实验研究[J].实用肿瘤杂志,2005,20(3):204-206. 被引量:6
  • 2汪进,何放亭,曾志雄,方宏勋,肖培根,韩锐,杨梦甦.紫杉醇诱导人乳腺癌M CF-7细胞周期阻断及凋亡的基因表达谱分析(英文)[J].药学学报,2005,40(12):1099-1104. 被引量:7
  • 3Reinhardt HC,Schumacher B.The P53 network:cellular and systemic DNA damage responses in aging and cancer [J].Trends Genet,2012,28(3):128-136.
  • 4Idogawa M,Sasaki Y,Suzuki H,et al.A single recombinant adenovirus exprssing p53 and p21-targeting artificial microRNAs efficiently induces apoptosis in human cancer cells[J].Clin Cancer Res,2009,15(11):3725-3732.
  • 5Ren SP,Wang L,Wang H,et al.Gene therapy for human nasopharyngeal carcinoma by adenovirus-mediated transfer of human p53,GM-CSF,and B7-1 genes in a mouse xenograft tumor model [J].Cancer Biother Radiopharm,2008,23(5):591-602.
  • 6Schramek D,Leibbrandt A,Sigl V,et al.Osteoclast differentiation factor RANKL controls development of progestin-driven mammary cancer [J].Nature,2010,468(7320):98-102.
  • 7Bourdon JC,Laurenzi VD,Melino G,et al.p53:25 years of research and more questions to answer [J].Cell Death Differenti,2003,10(4):397-399.
  • 8Kastan MB.Wild-type p53:tumors can' t stand it [J].Cell,2007,128(5):837-840.
  • 9Jin X,Burke W,Rottunan K,et al.Resistance to p53-mediated growth suppression in human ovarian cancer cells retain endogenous wild-type p53.Anticancer Research,2002,22(7):659-664.
  • 10Inoue K,Kurabayashi A,Shuin T,et al.Overexpression of p53 protein in human tumors [J].Med Mol M orphol,2012,45(3):115-123.

共引文献478

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部