Expression and Clinical Significance of YAP, TAZ, and AREG in Hepatocellular Carcinoma

被引:44
作者
Han, Su-xia [1 ]
Bai, E. [2 ]
Jin, Gui-hua [1 ]
He, Chen-chen [1 ]
Guo, Xi-jing [1 ]
Wang, Li-juan [1 ]
Li, Meng [1 ]
Ying, Xia [1 ]
Zhu, Qing [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Coll Med, Dept Med Oncol, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Coll Med, Ctr Maternal & Child Hlth, Xian 710061, Shaanxi, Peoples R China
关键词
YES-ASSOCIATED PROTEIN; GROWTH-FACTOR; LIVER-CANCER; AMPHIREGULIN; ONCOGENE; PROLIFERATION; PATHWAY; SIZE;
D O I
10.1155/2014/261365
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose. Yes-associated protein (YAP) and PDZ-binding motif (TAZ) are two important effectors of Hippo pathway controlling the balance of organ size and carcinogenesis. Amphiregulin (AREG) is a member of the epidermal growth factor family, a direct target gene of YAP and TAZ. The role of these proteins in hepatocellular carcinoma (HCC) is unclear. Methods. The expression of YAP, TAZ, and AREG in HCC was analyzed by immunohistochemical staining. The level of secreted serum AREG was also assayed by enzyme-linked immunosorbent (ELISA) assay. Results. YAP, TAZ, and AREG were expressed in 69.2% (27/39), 66.7% (26/39), and 61.5% (24/39) of HCC patients. The expression of YAP was significantly correlated with Edmondson stage (P > 0.05), serum AFP level (P > 0.05), and HCC prognosis (P > 0.05). AREG expression was also significantly correlated with Edmondson stage (P > 0.05) and serum AFP level (P > 0.05). In addition, the expression of serum AREG was higher than serum AFP in HCC patients. Further multivariate analysis showed that YAP expression was an independent prognostic factor that significantly affected the overall survival of HCC patients. Conclusions. YAP maybe an independent prognostic indicator for HCC patients and serum AREG may be a serological biomarker of HCC.
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页数:10
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共 21 条
[1]   Yes-associated protein (YAP) increases chemosensitivity of hepatocellular carcinoma cells by modulation of p53 [J].
Bai, Nan ;
Zhang, Chunyan ;
Liang, Ning ;
Zhang, Zhuhong ;
Chang, Antao ;
Yin, Jing ;
Li, Zongjin ;
Li, Na ;
Tan, Xiaoyue ;
Luo, Na ;
Luo, Yunping ;
Xiang, Rong ;
Li, Xiru ;
Reisfeld, Ralph A. ;
Stupack, Dwayne ;
Lv, Dan ;
Liu, Chenghu .
CANCER BIOLOGY & THERAPY, 2013, 14 (06) :511-520
[2]   Amphiregulin:: A new growth factor in hepatocarcinogenesis [J].
Berasain, C. ;
Castillo, J. ;
Perugorria, M. J. ;
Prieto, J. ;
Avila, M. A. .
CANCER LETTERS, 2007, 254 (01) :30-41
[3]   The transcriptional coactivator TAZ regulates mesenchymal differentiation in malignant glioma [J].
Bhat, Krishna P. L. ;
Salazar, Katrina L. ;
Balasubramaniyan, Veerakumar ;
Wani, Khalida ;
Heathcock, Lindsey ;
Hollingsworth, Faith ;
James, Johanna D. ;
Gumin, Joy ;
Diefes, Kristin L. ;
Kim, Se Hoon ;
Turski, Alice ;
Azodi, Yasaman ;
Yang, Yuhui ;
Doucette, Tiffany ;
Colman, Howard ;
Sulman, Erik P. ;
Lang, Frederick F. ;
Rao, Ganesh ;
Copray, Sjef ;
Vaillant, Brian D. ;
Aldape, Kenneth D. .
GENES & DEVELOPMENT, 2011, 25 (24) :2594-2609
[4]   Amphiregulin contributes to the transformed phenotype of human hepatocellular carcinoma cells [J].
Castillo, Josefa ;
Erroba, Elena ;
Perugorria, Maria J. ;
Santamaria, Monica ;
Lee, David C. ;
Prieto, Jesus ;
Avila, Matias A. ;
Berasain, Carmen .
CANCER RESEARCH, 2006, 66 (12) :6129-6138
[5]   A role for TAZ in migration, invasion, and tumorigenesis of breast cancer cells [J].
Chan, Siew Wee ;
Lim, Chun Jye ;
Guo, Ke ;
Ng, Chee Peng ;
Lee, Ian ;
Hunziker, Walter ;
Zeng, Qi ;
Hong, Wanjin .
CANCER RESEARCH, 2008, 68 (08) :2592-2598
[6]   Elucidation of a universal size-control mechanism in Drosophila and mammals [J].
Dong, Jixin ;
Feldmann, Georg ;
Huang, Jianbin ;
Wu, Shian ;
Zhang, Nailing ;
Comerford, Sarah A. ;
Gayyed, Mariana F. ;
Anders, Robert A. ;
Maitra, Anirban ;
Pan, Duojia .
CELL, 2007, 130 (06) :1120-1133
[7]   Role of YAP/TAZ in mechanotransduction [J].
Dupont, Sirio ;
Morsut, Leonardo ;
Aragona, Mariaceleste ;
Enzo, Elena ;
Giulitti, Stefano ;
Cordenonsi, Michelangelo ;
Zanconato, Francesca ;
Le Digabel, Jimmy ;
Forcato, Mattia ;
Bicciato, Silvio ;
Elvassore, Nicola ;
Piccolo, Stefano .
NATURE, 2011, 474 (7350) :179-U212
[8]   The hippo pathway in human upper gastrointestinal dysplasia and carcinoma: A novel oncogenic pathway [J].
Lam-Himlin D.M. ;
Daniels J.A. ;
Gayyed M.F. ;
Dong J. ;
Maitra A. ;
Pan D. ;
Montgomery E.A. ;
Anders R.A. .
Journal of Gastrointestinal Cancer, 2006, 37 (4) :103-109
[9]   The Hippo-Salvador pathway restrains hepatic oval cell proliferation, liver size, and liver tumorigenesis [J].
Lee, Kwang-Pyo ;
Lee, Joo-Hyeon ;
Kim, Tae-Shin ;
Kim, Tack-Hoon ;
Park, Hee-Dong ;
Byun, Jin-Seok ;
Kim, Min-Chul ;
Jeong, Won-Il ;
Calvisi, Diego F. ;
Kim, Jin-Man ;
Lim, Dae-Sik .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (18) :8248-8253
[10]   Identification of a Tumor Suppressor Relay between the FOXP3 and the Hippo Pathways in Breast and Prostate Cancers [J].
Li, Weiquan ;
Wang, Lizhong ;
Katoh, Hiroto ;
Liu, Runhua ;
Zheng, Pan ;
Liu, Yang .
CANCER RESEARCH, 2011, 71 (06) :2162-2171