SIRT5 downregulation is associated with poor prognosis in glioblastoma

被引:27
作者
Chen, Xi [1 ,2 ]
Xu, Zhijie [3 ]
Zeng, Shuangshuang [1 ,2 ]
Wang, Xiang [1 ,2 ]
Liu, Wanli [1 ,2 ]
Qian, Long [1 ,2 ]
Wei, Jie [1 ,2 ]
Yang, Xue [1 ,2 ]
Shen, Qiuying [1 ,2 ]
Gong, Zhicheng [1 ,2 ]
Yan, Yuanliang [1 ,2 ]
机构
[1] Cent S Univ, Dept Pharm, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
[2] Cent S Univ, Inst Rat & Safe Medicat Practices, Natl Clin Res Ctr Geriatr Disorders, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
[3] Cent S Univ, Dept Pathol, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Glioblastoma; SIRT5; prognosis; overall survival; DNA methylation; EPITHELIAL-MESENCHYMAL TRANSITION; CELL-PROLIFERATION; GENE-EXPRESSION; DNA METHYLATION; HEPATOCELLULAR-CARCINOMA; GENOME STABILITY; TUMOR-SUPPRESSOR; CANCER; BRAIN; OVEREXPRESSION;
D O I
10.3233/CBM-182197
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
OBJECTIVE: Sirtuins (SIRT) are NAD(+)-dependent protein deacetylases that are involved in the regulation of cancer-associated pathways. However, the biological role of these deacetylases remains elusive in glioblastoma (GBM). Here, we evaluated the effects of 7 sirtuins regarding their occurrence and prognostic value for GBM. METHODS: In this research, the effects of SIRT5 on the occurrence and prognosis of GBM were evaluated using integrative bioinformatics analyses. RESULTS: Based on comprehensive analyses of data obtained from web-based bioinformatics platforms, the data demonstrate that only SIRT5 expression is statistically decreased in GBM tissues. The clinical relevance analysis shows that downregulation of SIRT5 is significantly correlated with a shorter survival time. Moreover, the expression levels of SIRT5 were confirmed to be negatively associated with DNA methylation status. In addition, a protein-protein interaction network was constructed to determine the relationship of genes coexpressed with SIRT5. Functional enrichment analysis revealed that SIRT5 was potentially involved in epithelial-mesenchymal transition and in regulating cell communications. CONCLUSIONS: Collectively, our results indicate that SIRT5 acts as a potential suppresser during tumorigenesis, and suggest that SIRT5 may be a promising prognostic biomarker of GBM.
引用
收藏
页码:449 / 459
页数:11
相关论文
共 37 条
[1]   Assessing sirtuin expression in endometrial carcinoma and non-neoplastic endometrium [J].
Bartosch, Carla ;
Monteiro-Reis, Sara ;
Almeida-Rios, Diogo ;
Vieira, Renata ;
Castro, Armando ;
Moutinho, Manuel ;
Rodrigues, Marta ;
Graca, Ines ;
Lopes, Jose Manuel ;
Jeronimo, Carmen .
ONCOTARGET, 2016, 7 (02) :1144-1154
[2]   GlioVis data portal for visualization and analysis of brain tumor expression datasets [J].
Bowman, Robert L. ;
Wang, Qianghu ;
Carro, Angel ;
Verhaak, Roel G. W. ;
Squatrito, Massimo .
NEURO-ONCOLOGY, 2017, 19 (01) :139-141
[3]   Emerging Roles for SIRT5 in Metabolism and Cancer [J].
Bringman-Rodenbarger, Lauren R. ;
Guo, Angela H. ;
Lyssiotis, Costas A. ;
Lombard, David B. .
ANTIOXIDANTS & REDOX SIGNALING, 2018, 28 (08) :677-690
[4]   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
[5]   SIRT5 promotes cell proliferation and invasion in hepatocellular carcinoma by targeting E2F1 [J].
Chang, Liang ;
Xi, Liang ;
Liu, Yubin ;
Liu, Rui ;
Wu, Zhongshi ;
Jian, Zhixiang .
MOLECULAR MEDICINE REPORTS, 2018, 17 (01) :342-349
[6]   SIRT2 overexpression in hepatocellular carcinoma mediates epithelial to mesenchymal transition by protein kinase B/glycogen synthase kinase-3/-catenin signaling [J].
Chen, Juan ;
Chan, Anthony W. H. ;
To, Ka-Fai ;
Chen, Weixian ;
Zhang, Zhenzhen ;
Ren, Jihua ;
Song, Chunli ;
Cheung, Yue-Sun ;
Lai, Paul B. S. ;
Cheng, Suk-Hang ;
Ng, Margaret H. L. ;
Huang, Ailong ;
Ko, Ben C. B. .
HEPATOLOGY, 2013, 57 (06) :2287-2298
[7]   The epithelial-mesenchymal transition (EMT) is regulated by oncoviruses in cancer [J].
Chen, Xue ;
Bode, Ann M. ;
Dong, Zigang ;
Cao, Ya .
FASEB JOURNAL, 2016, 30 (09) :3001-3010
[8]   SIRT1 promotes epithelial-mesenchymal transition and metastasis in colorectal cancer by regulating Fra-1 expression [J].
Cheng, Feifei ;
Su, Li ;
Yao, Chao ;
Liu, Limei ;
Shen, Junjie ;
Liu, Chungang ;
Chen, Xuejiao ;
Luo, Yongli ;
Jiang, Lupin ;
Shan, Juanjuan ;
Chen, Jun ;
Zhu, Wei ;
Shao, Jimin ;
Qian, Cheng .
CANCER LETTERS, 2016, 375 (02) :274-283
[9]   SCD1 Confers Temozolomide Resistance to Human Glioma Cells via the Akt/GSK3β/β-Catenin Signaling Axis [J].
Dai, Shuang ;
Yan, Yuanliang ;
Xu, Zhijie ;
Zeng, Shuangshuang ;
Qian, Long ;
Huo, Lei ;
Li, Xuejun ;
Sun, Lunquan ;
Gong, Zhicheng .
FRONTIERS IN PHARMACOLOGY, 2018, 8
[10]   Wanderer, an interactive viewer to explore DNA methylation and gene expression data in human cancer [J].
Diez-Villanueva, Anna ;
Mallona, Izaskun ;
Peinado, Miguel A. .
EPIGENETICS & CHROMATIN, 2015, 8