TY - JOUR
T1 - High expression of TAZ serves as a novel prognostic biomarker and drives cancer progression in renal cancer
AU - Ruan, Hailong
AU - Bao, Lin
AU - Song, Zhengshuai
AU - Wang, Keshan
AU - Cao, Qi
AU - Tong, Junwei
AU - Cheng, Gong
AU - Xu, Tianbo
AU - Chen, Xuanyu
AU - Liu, Di
AU - Yang, Hongmei
AU - Chen, Ke
AU - Zhang, Xiaoping
N1 - Funding Information:
This study was supported by the National Natural Science Foundation of China (Grant No. 81874090 , 81702517 , 81672528 and 81672524 ) and Wuhan Union Hospital Scientific Research Fund (Free Innovation Pre-Research Fund, Grant no. 000005001 ).
Publisher Copyright:
© 2019
PY - 2019/3/15
Y1 - 2019/3/15
N2 - Renal cell carcinomas are a group of most common renal malignancies whose clinical intervention is complicated by the lack of early diagnosis and reliable prognosis biomarkers, insensitive radiotherapy and chemotherapy and expensive molecular-targeted drugs. Transcriptional coactivator TAZ has been implicated in the formation and development of various malignancies. However, the biological characteristics and function of TAZ in renal cell carcinoma are still unclear. We attempted to evaluate the potential of TAZ as a promising diagnostic and prognostic molecular marker for renal cell carcinoma. In our study, we confirmed that TAZ was frequently elevated in renal cancer tissues and cells, consistent with the results of the publicly available cancer database. Moreover, elevated TAZ expression was positively correlated with poor overall survival time, high Fuhrman grade and distant metastasis. Our receiver operating characteristic curves analysis showed that high TAZ expression could distinguish renal cancer patients from normal persons (p < 0.0001). Kaplan-Meier curves demonstrated that high TAZ expression predicted poor overall survival (p < 0.0001). Multivariate regression analysis indicated that TAZ expression could be an independent prognostic factor (p = 0.002) in patients with renal cancer. Finally, the functional roles of TAZ knockdown were examined in renal cancer cell lines and nude mice subcutaneous tumor models. In conclusion, our results suggest that TAZ may serve as a promising diagnostic and prognostic molecular marker for patients with renal cancer. Moreover, TAZ may represent a novel clinical therapeutic target.
AB - Renal cell carcinomas are a group of most common renal malignancies whose clinical intervention is complicated by the lack of early diagnosis and reliable prognosis biomarkers, insensitive radiotherapy and chemotherapy and expensive molecular-targeted drugs. Transcriptional coactivator TAZ has been implicated in the formation and development of various malignancies. However, the biological characteristics and function of TAZ in renal cell carcinoma are still unclear. We attempted to evaluate the potential of TAZ as a promising diagnostic and prognostic molecular marker for renal cell carcinoma. In our study, we confirmed that TAZ was frequently elevated in renal cancer tissues and cells, consistent with the results of the publicly available cancer database. Moreover, elevated TAZ expression was positively correlated with poor overall survival time, high Fuhrman grade and distant metastasis. Our receiver operating characteristic curves analysis showed that high TAZ expression could distinguish renal cancer patients from normal persons (p < 0.0001). Kaplan-Meier curves demonstrated that high TAZ expression predicted poor overall survival (p < 0.0001). Multivariate regression analysis indicated that TAZ expression could be an independent prognostic factor (p = 0.002) in patients with renal cancer. Finally, the functional roles of TAZ knockdown were examined in renal cancer cell lines and nude mice subcutaneous tumor models. In conclusion, our results suggest that TAZ may serve as a promising diagnostic and prognostic molecular marker for patients with renal cancer. Moreover, TAZ may represent a novel clinical therapeutic target.
KW - Clear cell renal cell carcinoma
KW - Diagnostic biomarker
KW - Prognostic biomarker
KW - TAZ
KW - Therapeutic target
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U2 - 10.1016/j.yexcr.2019.02.001
DO - 10.1016/j.yexcr.2019.02.001
M3 - Article
C2 - 30731073
AN - SCOPUS:85061395582
SN - 0014-4827
VL - 376
SP - 181
EP - 191
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 2
ER -