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Research on Regulation of Receptor Signalling Pathway of HeLa Cells by Clock Molecule DEC1

机译:时钟分子DEC1对HELA细胞受体信号通路调控的研究

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Objective: To make a study of the key factors from the Src to the nuclear transcription factor ERK signaling pathway as the target and to explore the role of DEC1 mediated ERK signaling pathway in cervical cancer and its mechanism. Methods: On the basis of screening DEC1 positive cells, the Hela cells with the highest positive rate of FRtt and the lowest DEC1 positive rate of MCF-7 cells were used as the experimental objects, and the growth of cervical cancer cells was detected by cell counting. Results: Src ERK1 and C Hela cells, Jun mRNA relative expression was significantly lower than that in MCF-7 cells, the differences were statistically significant (P<0.05): Hela and MCF-7 cells ERK2 and C - Fos mRNA relative expression was no significant difference (P>0.05). Conclusion: DEC1 can down regulate the expression of ERK upstream factor Src and protein in Hela cells of cervical cancer cell line mRNA, suggesting that DEC1 has other intermediate factors in the activation of ERK signaling pathway.
机译:目的:探讨SRC到核转录因子ERK信号通路的关键因素作为目标,探讨DEC1介导的ERK信号通路在宫颈癌及其机制中的作用。方法:在筛选DEC1阳性细胞的基础上,使用具有最高的FRTT阳性率和MCF-7细胞的最低DEC1阳性率的HELA细胞作为实验对象,细胞检测宫颈癌细胞的生长数数。结果:SRC ERK1和C HeLa细胞,Jun mRNA相对表达明显低于MCF-7细胞中,差异有统计学意义(P <0.05):HELA和MCF-7细胞ERK2和C - FOS mRNA相对表达是没有显着差异(p> 0.05)。结论:DEC1可以降低ERK上游因子SRC和蛋白在宫颈癌细胞系mRNA的HELA细胞中的表达,表明DEC1在ERK信号通路的激活中具有其他中间因素。

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