Overexpression of yes‐associated protein contributes to progression and poor prognosis of non‐small‐cell lung cancer

Cancer Science - Tập 101 Số 5 - Trang 1279-1285 - 2010
Yang Wang1, Qianze Dong1, Qingfu Zhang1, Zixuan Li1, Enhua Wang1, Xueshan Qiu1
1Department of Pathology, First Affiliated Hospital of China Medical University and Department of Pathology, College of Basic Medical Sciences, China Medical University, Shenyang, China.

Tóm tắt

Yes‐associated protein (YAP), the nuclear effector of the Hippo pathway, is a key regulator of organ size and a candidate human oncogene. This study aimed to assess the clinical significance and biological functions of YAP in non‐small‐cell lung cancer (NSCLC). We investigated the expression of YAP in 92 cases of NSCLC tissue by immunohistochemistry and found that YAP was expressed in 66.3% (61/92) cases and predominantly presented in the nucleus. The expression of YAP in NSCLC was significantly correlated with p‐TNM stage (P = 0.0037) and lymph node metastasis (P = 0.0093). Importantly, YAP expression was associated with short overall survival. Further study in NSCLC cell lines in which YAP was either overexpressed or depleted confirmed that YAP markedly promoted cell proliferation and invasion. These results indicate that YAP plays an important role in NSCLC and might be a useful therapeutic target of NSCLC.

(Cancer Sci 2010; 101: 1279–1285)

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10.1016/S1535-6108(02)00027-2

10.3322/canjclin.57.1.43

10.1056/NEJMoa011954

10.1016/j.cell.2007.07.019

10.1016/j.cell.2005.06.007

10.1016/j.cell.2006.01.005

10.1093/emboj/18.9.2551

10.1016/j.molcel.2005.04.008

10.1074/jbc.M401070200

10.1038/sj.emboj.7600073

10.1074/jbc.M305597200

10.1074/jbc.M008568200

10.1074/jbc.M010484200

10.1128/MCB.26.1.77-87.2006

10.1016/j.cell.2006.05.030

10.1073/pnas.0605579103

10.1200/JCO.2006.06.3701

10.1016/j.humpath.2008.04.012

10.1002/cncr.24495

10.1101/gad.1602907

10.1016/j.cub.2007.10.039

10.1038/sj.cdd.4402226

10.1074/jbc.M400126200

10.1016/j.humpath.2008.06.023

10.1016/j.devcel.2008.01.007

10.1038/cdd.2008.108

10.1016/j.molcel.2007.08.008

10.1038/ncb1543