YAP1 在结直肠癌中的表达通过其靶基因赋予侵袭性表型。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-01-01 Epub Date: 2024-01-23 DOI:10.1080/15384101.2024.2309017
Haoyuan Chen, Yangyang Shang, Xia Li, Rongquan Wang
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引用次数: 0

摘要

是相关蛋白1(YAP1)是Hippo通路的下游效应因子,在多种恶性肿瘤中过度表达。我们回顾性分析了 TCGA 数据库中的 447 个结直肠癌(CRC)样本,以确定 YAP1 表达水平与 CRC 患者预后之间的相关性。使用含有 YAP1 插入物的慢病毒颗粒构建了强化表达 YAP1 的 CRC 细胞系。YAP1在CRC癌组织中高表达,并与CRC患者的远处转移有关。Kaplan - Meier分析表明,YAP1表达较高组(n = 104)的CRC患者的无病生存期(DFS)和总生存期(OS)比YAP1表达较低组(n = 343)更差(p = 0.008和p = 0.022)。单变量和多变量分析表明,YAP1表达升高可预测侵袭性表型,是影响CRC患者OS和DFS的独立指标。YAP1在CRC细胞中过度表达会显著增强其迁移和侵袭能力,而AXL、CTGF或CYR61干扰可逆转这种能力。研究表明,YAP1会影响CRC患者的预后,并通过其靶基因AXL、CTGF和CYR61控制CRC细胞的侵袭和迁移能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
YAP1 expression in colorectal cancer confers the aggressive phenotypes via its target genes.

Yes-associated protein1 (YAP1), a downstream effector of the Hippo pathway, is over-expressed in several types of malignancies. We analyzed retrospectively the TCGA database using 447 colorectal cancer (CRC) samples to determine the correlation between YAP1 expression level and CRC patient prognosis. YAP1-enforced expressed CRC cell lines were constructed using the lentivirus particles containing a YAP1 insert. YAP1 was highly expressed in CRC cancerous tissues and is associated with distant metastasis of CRC patients. Kaplan - Meier analysis indicated that CRC patients with a higher YAP1 expression group (n = 104) had worse disease-free survival (DFS) and overall survival (OS) than lower YAP1 expression group (n = 343) (p = 0.008 and p = 0.022). Univariate and multivariate analysis indicated that the elevated YAP1 expression predicted the aggressive phenotype and was an independent indicator for OS and DFS of CRC patients. YAP1 over-expression in CRC cells enhanced their migration and invasion significantly which can be reversed by AXL, CTGF, or CYR61 interference. The study suggested that YAP1 affected the prognosis of CRC patients and controlled the abilities of invasion and migration of CRC cells via its target genes AXL, CTGF, and CYR61.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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