Department of Molecular Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University,Bunkyo-ku, Tokyo 113-8510, Japan.
Carcinogenesis. 2011 Mar;32(3):389-98. doi: 10.1093/carcin/bgq254. Epub 2010 Nov 26.
Yes-associated protein (YAP), the nuclear effector of the Hippo pathway, is a key regulator of organ size and a candidate human oncogene located at chromosome 11q22. Since we previously reported amplification of 11q22 region in esophageal squamous cell carcinoma (ESCC), in this study we focused on the clinical significance and biological functions of YAP in this tumor. Frequent overexpression of YAP protein was observed in ESCC cells including those with a robust amplicon at position 11q22. Overexpression of the YAP protein was frequently detected in primary tumors of ESCC as well. Patients with YAP-overexpressing tumors had a worse overall rate of survival than those with non-expressing tumors, and YAP positivity was independently associated with a worse outcome in the multivariate analysis. Further analyses in cells in which YAP was either overexpressed or depleted confirmed that cell proliferation was promoted in a YAP isoform-independent but YAP expression level-dependent manner. YAP depletion inhibited cell proliferation mainly in the G(0)-G(1) phase and induced an increase in CDKN1A/p21 transcription but a decrease in BIRC5/survivin transcription. Our results indicate that YAP is a putative oncogene in ESCC and it represents a potential diagnostic and therapeutic target.
Yes 相关蛋白 (YAP) 是 Hippo 通路的核效应物,是调节器官大小的关键因子,也是位于染色体 11q22 的人类候选癌基因。由于我们之前报道了食管鳞状细胞癌 (ESCC) 中 11q22 区域的扩增,因此在这项研究中,我们专注于 YAP 在这种肿瘤中的临床意义和生物学功能。YAP 蛋白在 ESCC 细胞中频繁过表达,包括在位置 11q22 处具有强扩增子的细胞。YAP 蛋白的过表达也经常在 ESCC 的原发性肿瘤中检测到。YAP 过表达肿瘤患者的总生存率明显低于非表达肿瘤患者,并且 YAP 阳性在多变量分析中与不良预后独立相关。对 YAP 过表达或耗竭的细胞进行的进一步分析证实,细胞增殖以 YAP 同工型非依赖性但 YAP 表达水平依赖性的方式促进。YAP 耗竭主要在 G0-G1 期抑制细胞增殖,并诱导 CDKN1A/p21 转录增加,但 BIRC5/survivin 转录减少。我们的结果表明,YAP 是 ESCC 中的一个推定癌基因,它代表了一个潜在的诊断和治疗靶标。