Integrative Analysis of Sirtuins and Their Prognostic Significance in Clear Cell Renal Cell Carcinoma

被引:18
作者
Tan, Ying [1 ]
Li, Bijuan [1 ]
Peng, Fang [2 ]
Gong, Guanghui [3 ]
Li, Ning [1 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Blood Transfus, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Hosp, NHC Key Lab Canc Prote, Changsha, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Dept Pathol, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
sirtuins; epigenetics; TCGA; cancer; clear cell renal cell carcinoma; TUMOR-SUPPRESSOR; CANCER; EXPRESSION; SIRT6; SURVIVAL; PROLIFERATION; RESISTANCE; GROWTH;
D O I
10.3389/fonc.2020.00218
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sirtuins, class III histone deacetylases, are involved in multiple biological processes in cancer initiation and progression. However, the diverse expression patterns and prognostic values of sirtuins in cancers have yet to be elucidated. In this study, we first evaluated the expression and prognostic values of sirtuins in multiple cancer cohorts using publicly available TCGA pan-cancer datasets. Pan-cancer survival analysis indicated that 6 out of 7 sirtuin family members were significant associated with prognosis of clear cell renal cell carcinoma (KIRC) patients. SIRT1, SIRT3, SIRT4, and SIRT5 were associated with favorable prognosis of KIRC patients, while SIRT6 and SIRT7 were associated with unfavorable prognosis. The expression levels of SIRT4 and SIRT5 in KIRC tissues were lower than that in normal tissues, while SIRT6 and SIRT7 were higher in KIRC tissues. The expression levels of SIRT1, SIRT3, SIRT5, SIRT6, and SIRT7 were significantly correlated with tumor stage and histological grade. DNA methylation may contribute to the dysregulation of sirtuins. Finally, GSEA was conducted to predict the potential functions of sirtuins in KIRC. Our results may provide novel insights for the development of sirtuins-based cancer therapy in KIRC.
引用
收藏
页数:10
相关论文
共 50 条
[1]   SIRT6 expression is associated with poor prognosis and chemosensitivity in patients with non-small cell lung cancer [J].
Azuma, Yoko ;
Yokobori, Takehiko ;
Mogi, Akira ;
Altan, Bolag ;
Yajima, Toshiki ;
Kosaka, Takayuki ;
Onozato, Ryoichi ;
Yamaki, Ei ;
Asao, Takayuki ;
Nishiyama, Masahiko ;
Kuwano, Hiroyuki .
JOURNAL OF SURGICAL ONCOLOGY, 2015, 112 (02) :231-237
[2]   Upregulation of SIRT6 predicts poor prognosis and promotes metastasis of non-small cell lung cancer via the ERK1/2/MMP9 pathway [J].
Bai, Lihong ;
Lin, Gengpeng ;
Sun, Longhua ;
Liu, Yangli ;
Huang, Xinyan ;
Cao, Chuangjie ;
Guo, Yubiao ;
Xie, Canmao .
ONCOTARGET, 2016, 7 (26) :40377-40386
[3]   DNA methylation and gene silencing in cancer [J].
Baylin S.B. .
Nature Clinical Practice Oncology, 2005, 2 (Suppl 1) :S4-S11
[4]   RETRACTED: MicroRNA-9 inhibits the proliferation and migration of malignant melanoma cells via targeting sirituin 1 (Retracted article. See vol. 22, 2021) [J].
Bu, Pingyuan ;
Luo, Chengqun ;
He, Quanyong ;
Yang, Ping ;
Li, Xi ;
Xu, Dan .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2017, 14 (02) :931-938
[5]   Dual Tumor Suppressor and Tumor Promoter Action of Sirtuins in Determining Malignant Phenotype [J].
Carafa, Vincenzo ;
Altucci, Lucia ;
Nebbioso, Angela .
FRONTIERS IN PHARMACOLOGY, 2019, 10
[6]   The cBio Cancer Genomics Portal: An Open Platform for Exploring Multidimensional Cancer Genomics Data [J].
Cerami, Ethan ;
Gao, Jianjiong ;
Dogrusoz, Ugur ;
Gross, Benjamin E. ;
Sumer, Selcuk Onur ;
Aksoy, Buelent Arman ;
Jacobsen, Anders ;
Byrne, Caitlin J. ;
Heuer, Michael L. ;
Larsson, Erik ;
Antipin, Yevgeniy ;
Reva, Boris ;
Goldberg, Arthur P. ;
Sander, Chris ;
Schultz, Nikolaus .
CANCER DISCOVERY, 2012, 2 (05) :401-404
[7]   UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses [J].
Chandrashekar, Darshan S. ;
Bashel, Bhuwan ;
Balasubramanya, Sai Akshaya Hodigere ;
Creighton, Chad J. ;
Ponce-Rodriguez, Israel ;
Chakravarthi, Balabhadrapatruni V. S. K. ;
Varambally, Sooryanarayana .
NEOPLASIA, 2017, 19 (08) :649-658
[8]   SIRT5 downregulation is associated with poor prognosis in glioblastoma [J].
Chen, Xi ;
Xu, Zhijie ;
Zeng, Shuangshuang ;
Wang, Xiang ;
Liu, Wanli ;
Qian, Long ;
Wei, Jie ;
Yang, Xue ;
Shen, Qiuying ;
Gong, Zhicheng ;
Yan, Yuanliang .
CANCER BIOMARKERS, 2019, 24 (04) :449-459
[9]   SIRT1 downregulated FGB expression to inhibit RCC tumorigenesis by destabilizing STAT3 [J].
Chen, Yanbing ;
Zhu, Ying ;
Sheng, Yanling ;
Xiao, Juhua ;
Xiao, Yu ;
Cheng, Na ;
Chai, Yong ;
Wu, Xiaoping ;
Zhang, Shouhua ;
Xiang, Tianxin .
EXPERIMENTAL CELL RESEARCH, 2019, 382 (2-3)
[10]   Mitochondrial Sirt3 supports cell proliferation by regulating glutamine-dependent oxidation in renal cell carcinoma [J].
Choi, Jieun ;
Koh, Eunjin ;
Lee, Yu Shin ;
Lee, Hyun-Woo ;
Kang, Hyeok Gu ;
Yoon, Young Eun ;
Han, Woong Kyu ;
Choi, Kyung Hwa ;
Kim, Kyung-Sup .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 474 (03) :547-553