Yes-Associated Protein Contributes to the Development of Human Cutaneous Squamous Cell Carcinoma via Activation of RAS

被引:46
|
作者
Jia, Jinjing [1 ]
Li, Changji [1 ]
Luo, Suju [2 ]
Liu-Smith, Feng [3 ,4 ]
Yang, Jiao [1 ]
Wang, Xin [1 ]
Wang, Nanping [5 ]
Lai, Baochang [5 ]
Lei, Ting [5 ,6 ]
Wang, Qiongyu [1 ]
Xiao, Shengxiang [1 ]
Shao, Yongping [7 ,8 ]
Zheng, Yan [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Dermatol, Affiliated Hosp 2, Sch Med, 157 Xiwu Rd, Xian 710004, Peoples R China
[2] Tianjin Med Univ, Gen Hosp, Dept Dermatol, Tianjin, Peoples R China
[3] Univ Calif Irvine, Dept Epidemiol, Irvine, CA USA
[4] Univ Calif Irvine, Dept Med, Irvine, CA 92717 USA
[5] Xi An Jiao Tong Univ, Hlth Sci Ctr, Cardiovasc Res Ctr, Sch Basic Med Sci, Xian, Peoples R China
[6] Xi An Jiao Tong Univ, Hlth Sci Ctr, Dept Pathol, Sch Basic Med Sci, Xian, Peoples R China
[7] Xi An Jiao Tong Univ, Key Lab Biomed Informat Engn, Minist Educ, Sch Life Sci & Technol, Xian, Peoples R China
[8] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
PATHWAY TRANSCRIPTIONAL COACTIVATOR; ORGAN SIZE CONTROL; HIPPO PATHWAY; HEPATOCELLULAR-CARCINOMA; CONFERS RESISTANCE; CANCER DEVELOPMENT; LIVER-CANCER; HUMAN-SKIN; YAP; EXPRESSION;
D O I
10.1016/j.jid.2016.02.005
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Cutaneous squamous cell carcinoma (cSCC) is one of the most common skin malignant tumors with an increasing incidence. Studies have shown that Yes-associated protein (YAP) participates in the development of a variety of tumors as an oncogene, but to our knowledge its role in cSCC has not been reported. In this study, we used immunohistochemistry to show that YAP expression was elevated in cSCC samples of different stages versus in normal skin and that it was well correlated with the progression of the disease. Down-regulation of YAP in cSCC cell lines A431 and SCL-1 inhibited cell proliferation by inducing growth arrest during the G1/S phase transition, promoted apoptosis, and reduced invasion and migration abilities in vitro. Conversely, overexpression of YAP promoted cell proliferation and protected cells against basal and chemotherapy-induced apoptosis. These oncogenic effects of YAP were associated with activation of the RAS protein and its downstream AKT and ERK. Using a mouse xenograft model, we further showed that YAP depletion inhibited cSCC tumor growth in vivo. Our results suggested that YAP is involved in the carcinogenesis and development of cSCC and that it may serve as a biomarker or therapeutic target of this disease.
引用
收藏
页码:1267 / 1277
页数:11
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