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下调STYK1基因表达可抑制结直肠癌细胞生长与侵袭
引用本文:唐佳佳,叶林.下调STYK1基因表达可抑制结直肠癌细胞生长与侵袭[J].第三军医大学学报,2017(17).
作者姓名:唐佳佳  叶林
作者单位:重庆医科大学附属第一医院重症医学科,重庆,400016
摘    要:目的 探讨STYK1基因下调对结直肠癌细胞HCT-15增殖、凋亡和迁移以及MEK/ERK和PI3 K/AKT信号通路的影响.方法 采用基因干扰技术抑制结直肠癌细胞HCT-15中STYK1的表达,Western blot检测抑制效果,CCK-8检测STYK1表达下调对HC-T15细胞增殖的影响,流式细胞仪检测STYK1表达下调对HC-T15细胞凋亡的影响,Transwell小室实验检测STYK1表达下调对HCT-15细胞侵袭的影响,通过Western blot检测STYK1表达下调对HCT-15细胞MEK/ERK和PI3 K/AKT信号通路活性的影响.结果 与干扰对照组相比,STYK1表达下调明显抑制HCT-15细胞增殖活性(P<0.01)和侵袭能力(P<0.01),并诱导细胞凋亡(P<0.01);同时,STYK1表达下调明显抑制HCT-15细胞ERK1/2和AKT蛋白的磷酸水平.结论 STYK1基因干扰可以抑制结直肠癌细胞的增殖和侵袭,并诱导凋亡,其机制可能与抑制MEK/ERK和PI3K/AKT信号通路活性有关.

关 键 词:miR-671  直肠癌  增殖  迁移

STYK1 down-regulation suppresses colorectal cancer cell growth and invasion in vitro
TANG Jiajia,YE Lin.STYK1 down-regulation suppresses colorectal cancer cell growth and invasion in vitro[J].Acta Academiae Medicinae Militaris Tertiae,2017(17).
Authors:TANG Jiajia  YE Lin
Abstract:Objective To determine the effects of down-regulating serine/threonine/tyrosine kinase 1 (STYK1) on the proliferation,apoptosis and invasion and on MEK/ERK and PI3K/AKT signaling pathways in human colorectal cancer cell line HCT-15.Methods The expression of STYK1 protein was downregulated by RNA interference technique in HCT-15 cells.Then,the STYK1 protein expression was detected by Western blotting.CCK-8 assay was used to measure the effect of STYK1 down-regulation on the proliferation of the cells,flow cytometry was employed to detect the cell apoptosis,and Transwell chamber assay was adopted for cell invasion ability.The expression levels of p-ERK1/2 and p-AKT were detected by Western blotting.Results Compared with the siRNA NC group,STYK1 down-regulation significantly inhibited the proliferation (P < 0.01) and invasion (P < 0.01),induced cell apoptosis (P < 0.01),and suppressed the expression levels of p-ERK1/2 and p-AKT in the HCT cells transfected with STYK1 siRNA (P <0.01).Conclusion STYK1 down-regulation inhibits the proliferation and invasion and induces the apoptosis in colorectal cancer cells,which may be related to its inhibition on the MEK/ERK and PI3K/AKT signaling pathways.
Keywords:serine/threonine/tyrosine kinase 1  colorectal cancer  proliferation  invasion
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