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Rho GDP‐dissociation inhibitor α is a potential prognostic biomarker and controls telomere regulation in colorectal cancer

机译:Rho GDP解离抑制剂α是潜在的预后生物标志物,可控制结直肠癌中端粒的调控

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Rho GDP-dissociation inhibitor α (RhoGDIα) is an essential regulator for Rho GTPases. Although RhoGDI α may serve as an oncogene in colorectal cancer (CRC), the underlying mechanism is still unclear. We investigated the function, mechanism, and clinical significance of RhoGDIα in CRC progression. We founded that downregulation of RhoGDIα repressed CRC cell proliferation, motility, and invasion. Overexpression of RhoGDIα increased DNA damage response signals at telomeres, and led to telomere shortening in CRC cells, also being validated in 26 pairs of CRC tissues. Mechanistic studies revealed that RhoGDIα could promote telomeric repeat factor 1 (TRF1) expression through the phosphatidylinositol 3-kinase–protein kinase B signal pathway. Moreover, RhoGDIα protein levels were strongly correlated with TRF1 in CRC tissues. A cohort of 297 CRC samples validated the positive relationship between RhoGDIα and TRF1, and revealed that RhoGDIα and TRF1 levels were negatively associated with CRC patients' survival. Taken together, our results suggest that RhoGDIα regulate TRF1 and telomere length and may be novel prognostic biomarkers in colorectal cancer.
机译:Rho GDP离解抑制剂α(RhoGDIα)是Rho GTPases的重要调节剂。尽管RhoGDIα可能在结直肠癌(CRC)中作为致癌基因,但其潜在机制仍不清楚。我们调查了RhoGDIα在CRC进展中的功能,机制和临床意义。我们发现RhoGDIα的下调抑制了CRC细胞的增殖,运动和侵袭。 RhoGDIα的过表达增加了端粒的DNA损伤反应信号,并导致CRC细胞中的端粒缩短,这在26对CRC组织中也得到了验证。机理研究表明,RhoGDIα可以通过磷脂酰肌醇3激酶-蛋白激酶B信号通路促进端粒重复因子1(TRF1)的表达。此外,RhoGDIα蛋白水平与CRC组织中的TRF1密切相关。 297个CRC样本队列验证了RhoGDIα和TRF1之间的正相关关系,并揭示RhoGDIα和TRF1水平与CRC患者的生存负相关。两者合计,我们的结果表明RhoGDIα调节TRF1和端粒的长度,可能是结直肠癌的新型预后生物标志物。

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