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首页> 外文期刊>Oncology letters >Expression and potential correlation among Forkhead box protein M1, Caveolin-1 and E-cadherin in colorectal cancer
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Expression and potential correlation among Forkhead box protein M1, Caveolin-1 and E-cadherin in colorectal cancer

机译:前叉箱蛋白M1,Caveolin-1和E-cadherin在结直肠癌中的表达及潜在相关性

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摘要

The aim of the present study was to investigate the expression and functions of Forkhead box protein M1 (FoxM1), Caveolin-1 (Cav-1) and E-cadherin in colorectal cancer (CRC), and to determine the correlations among these proteins in CRC development and progression. The protein expression of FoxM1, Cav-1 and E-cadherin was identified using a human CRC and normal tissue microarray. A standard immunohistochemistry assay was performed employing anti-FoxM1, anti-Cav-1 and anti-E-cadherin antibodies. The clinicopathological significance of FoxM1, Cav-1 and E-cadherin in CRC was determined, and correlations were investigated between FoxM1 and Cav-1, FoxM1 and E-cadherin, Cav-1 and E-cadherin, respectively. The level of FoxM1, Cav-1 and E-Cadherin protein expression in CRC was found to be associated with pathological grade, tumor clinical stages and the presence of metastasis, respectively. Elevated expression of FoxM1 and Cav-1 was observed in the CRC tissues, and a significant correlation was found between the two proteins in CRC. However, it was also observed that FoxM1 was overexpressed while E-cadherin expression was low, indicating that there was a negative correlation between FoxM1 expression and E-cadherin expression. Moreover, there was also a negative correlation between Cav-1 and E-cadherin expression. Overall, the elevated expression of FoxM1 and Cav-1 in a human CRC microarray provided novel clinical evidence to elucidate the fact that they may play a critical role in the development and progression of CRC by negatively regulating E-cadherin expression. Furthermore, the positive correlation between FoxM1 and Cav-1 suggested that the proteins may constitute a novel signaling pathway in human CRC.
机译:本研究的目的是研究叉头盒蛋白M1(FoxM1),小窝蛋白1(Cav-1)和E-钙粘蛋白在结直肠癌(CRC)中的表达和功能,并确定这些蛋白之间的相关性。 CRC的发展和进程。 FoxM1,Cav-1和E-cadherin的蛋白表达使用人CRC和正常组织微阵列鉴定。使用抗FoxM1,抗Cav-1和抗E-钙粘蛋白抗体进行了标准的免疫组织化学测定。确定了FoxM1,Cav-1和E-cadherin在CRC中的临床病理学意义,并研究了FoxM1和Cav-1,FoxM1和E-cadherin,Cav-1和E-cadherin之间的相关性。发现CRC中FoxM1,Cav-1和E-Cadherin蛋白的表达水平分别与病理分级,肿瘤临床分期和转移的发生有关。在CRC组织中观察到FoxM1和Cav-1的表达升高,并且在CRC中的两种蛋白之间发现了显着的相关性。但是,还观察到FoxM1过表达而E-cadherin表达低,表明FoxM1表达与E-cadherin表达呈负相关。此外,Cav-1与E-cadherin表达之间也呈负相关。总体而言,FoxM1和Cav-1在人CRC芯片中的表达升高提供了新的临床证据,阐明了它们可能通过负调控E-钙黏着蛋白的表达而在CRC的发生和发展中发挥关键作用。此外,FoxM1和Cav-1之间的正相关性表明该蛋白可能构成人类CRC中的新型信号通路。

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