CXC趋化因子受体4通过S期激酶相关蛋白2调控乳腺癌细胞周期的机制  被引量:5

CXC chemokine receptor 4 regulates breast cancer cell cycle through S phase kinase associated protein 2

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作  者:王海凤[1] 陈天天 王月月 李钰[1] 张凌宇[1] 丁勇兴[2] 陈素莲[3] 王文锐 杨清玲[3] 陈昌杰[3] 

机构地区:[1]蚌埠医学院临床检验诊断学实验中心,安徽蚌埠233000 [2]蚌埠市第三人民医院普外肿瘤科,安徽蚌埠233000 [3]蚌埠医学院生物化学与分子生物学教研室,安徽蚌埠233000 [4]蚌埠医学院生物技术教研室,安徽蚌埠233000

出  处:《浙江大学学报(医学版)》2017年第4期357-363,共7页Journal of Zhejiang University(Medical Sciences)

基  金:安徽省教育厅自然科学重大项目(KJ2015ZD29;KJ2016SD37);安徽省自然科学基金(1508085MH159);安徽省高校学科(专业)拔尖人才学术资助重点项目(gxbjZD2016069);安徽省蚌埠市科技计划项目(20150309);蚌埠医学院研究生创新项目(Byycxz1607)

摘  要:目的:探讨CXC趋化因子受体4(CXCR4)通过PI3K/Akt和ERK信号通路调控S期激酶相关蛋白2(Skp2)的表达,进而影响乳腺癌细胞周期的机制。方法:利用干扰及过表达技术下调或上调CXCR4的表达后,通过实时定量PCR和蛋白质印迹法检测CXCR4与Skp2调控的关联性;蛋白质印迹法检测CXCR4干扰及过表达后对信号蛋白及Skp2下游相关基因表达的影响;通过碘化丙啶(PI)染色法检测CXCR4、PI3K/Akt通路抑制剂LY294002及ERK通路抑制剂U0126对乳腺癌细胞周期的影响。结果:干扰CXCR4后,Skp2表达下调;过表达CXCR4后,Skp2表达上调。CXCR4可通过对信号蛋白的调控影响Skp2及Skp2下游相关基因的表达。干扰CXCR4后,G_0/G_1期细胞比例增加,S期细胞比例相应减少,CXCR4与LY294002及U0126联合作用对细胞周期的阻断更加明显。结论:CXCR4能够通过对信号蛋白PI3K/Akt及ERK的调控,影响Skp2及Skp2下游相关基因的表达,阻断CXCR4/Akt/Skp2或CXCR4/ERK/Skp2信号通路后可有效诱导细胞周期阻滞,从而抑制乳腺癌细胞的增殖。Objective: To investigate the effect of CXC chemokine receptor 4 (CXCR4) on cell cycle of breast cancer and its molecular mechanisms. Methods: The expression of CXCR4 and S phase kinase associated protein 2 (Skp2) was detected by real-time fluorescence quantitative PCR (fqRT-PCR) and Western blot in breast cancer cells. The expression of signal proteins and the downstream genes of Skp2 was detected by Western blot. The effect of CXCR4, PI3K/Akt pathway inhibitor LY294002 and ERK pathway inhibitor U0126 on cell cycle of breast cancer was detected by propidium iodide staining. Results: Skp2 was significantly down-regulated in CXCR4-downregulated cells and up-regulated in CXCR4-upregnlated cells. CXCR4 also regulated the expression of Skp2 and other downstream genes by signaling protein. The proportion of cells in G0/G1 phase increased and that in S phase declined in CXCR4-downregulated cell, and the effect was more significant when combined with the use of LY294002 or U0126. Conclusion: CXCR4 can affect cell cycle and inhibit the proliferation of breast cancer cells by regulating Skp2 gene expression through PI3K/Akt and ERK signaling pathway.

关 键 词:乳腺肿瘤/病理生理学 受体 CXCR4/生物合成 受体 CXCR4/遗传学 S期激酶相关蛋白质类/代谢 细胞系 肿瘤/代谢 细胞增殖 细胞周期 

分 类 号:R737.9[医药卫生—肿瘤]

 

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