MicroRNA expression signatures of stage, grade, and progression in clear cell RCC

被引:78
作者
Gowrishankar, Banumathy [1 ]
Ibragimova, Ilsiya [1 ]
Zhou, Yan [2 ]
Slifker, Michael J. [2 ]
Devarajan, Karthik [2 ]
Al-Saleem, Tahseen [3 ,4 ]
Uzzo, Robert G. [3 ,5 ]
Cairns, Paul [1 ,3 ]
机构
[1] Fox Chase Canc Ctr, Canc Epigenet Program, Philadelphia, PA 19111 USA
[2] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[3] Fox Chase Canc Ctr, Kidney Canc Keystone Program, Philadelphia, PA 19111 USA
[4] Fox Chase Canc Ctr, Dept Pathol, Philadelphia, PA 19111 USA
[5] Fox Chase Canc Ctr, Dept Surg, Philadelphia, PA 19111 USA
关键词
stage; microRNA; RCC; signatures; progression; expression; grade; clear cell RCC; miRNA; GENE-EXPRESSION; STEM-CELLS; CARCINOMA; DIFFERENTIATION; CANCER; IDENTIFICATION; NEPHRECTOMY; PATHWAYS; SURVIVAL; TARGETS;
D O I
10.4161/cbt.27314
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clear cell RCC is the most common, and more likely to metastasize, of the three main histological types of RCC. Pathologic stage is the most important prognostic indicator and nuclear grade can predict outcome within stages of localized RCC. Epithelial tumors are thought to accumulate a series of genetic and epigenetic changes as they progress through well-defined clinical and histopathological changes. MicroRNAs (miRNAs) are involved in the regulation of mRNA expression from many human genes and miRNA expression is dysregulated in cancer. To better understand the contribution of dysregulated miRNA expression to the progression and biology of ccRCC, we examined the differences in expression levels of 723 human miRNAs through a series of analyses by stage, grade, and disease progression status in a large series of 94 ccRCC. We found a consistent signature that included significant upregulation of miR-21-5p, 142-3p, let-7g-5p, let-7i-5p and 424-5p, as well as downregulation of miR-204-5p, to be associated with ccRCC of high stage, or high grade, or progression. Discrete signatures associated with each of stage, grade, or progression were also identified. The let-7 family was significantly downregulated in ccRCC compared with normal renal parenchyma. Expression of the 6 most significantly differentially expressed miRNAs between ccRCC was verified by stem-loop qRT-PCR. Pathways predicted as targets of the most significantly dysregulated miRNAs included signaling, epithelial cancers, metabolism, and epithelial to mesenchymal transition. Our studies help to further elucidate the biology underlying the progression of ccRCC and identify miRNAs for potential translational application.
引用
收藏
页码:329 / 341
页数:13
相关论文
共 53 条
[41]   SnapShot: MicroRNAs in Cancer [J].
Spizzo, Riccardo ;
Nicoloso, Milena S. ;
Croce, Carlo M. ;
Calin, George A. .
CELL, 2009, 137 (03) :586-U204
[42]   miR-99 Family of MicroRNAs Suppresses the Expression of Prostate-Specific Antigen and Prostate Cancer Cell Proliferation [J].
Sun, Dandan ;
Lee, Yong Sun ;
Malhotra, Ankit ;
Kim, Hak Kyun ;
Matecic, Mirela ;
Evans, Clive ;
Jensen, Roderick V. ;
Moskaluk, Christopher A. ;
Dutta, Anindya .
CANCER RESEARCH, 2011, 71 (04) :1313-1324
[43]   Mir193b-365 is essential for brown fat differentiation [J].
Sun, Lei ;
Xie, Huangming ;
Mori, Marcelo A. ;
Alexander, Ryan ;
Yuan, Bingbing ;
Hattangadi, Shilpa M. ;
Liu, Qingqing ;
Kahn, C. Ronald ;
Lodish, Harvey F. .
NATURE CELL BIOLOGY, 2011, 13 (08) :958-U198
[44]   An autoregulatory loop mediated by miR-21 and PDCD4 controls the AP-1 activity in RAS transformation [J].
Talotta, F. ;
Cimmino, A. ;
Matarazzo, M. R. ;
Casalino, L. ;
De Vita, G. ;
D'Esposito, M. ;
Di Lauro, R. ;
Verde, P. .
ONCOGENE, 2009, 28 (01) :73-84
[45]  
Tissot C, ANAL MIRNA CONTENT T
[46]   DIANA miRPath v.2.0: investigating the combinatorial effect of microRNAs in pathways [J].
Vlachos, Ioannis S. ;
Kostoulas, Nikos ;
Vergoulis, Thanasis ;
Georgakilas, Georgios ;
Reczko, Martin ;
Maragkakis, Manolis ;
Paraskevopoulou, Maria D. ;
Prionidis, Kostantinos ;
Dalamagas, Theodore ;
Hatzigeorgiou, Artemis G. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (W1) :W498-W504
[47]   Direct and sensitive miRNA profiling from low-input total RNA [J].
Wang, Hui ;
Ach, Robert A. ;
Curry, Bo .
RNA, 2007, 13 (01) :151-159
[48]   MicroRNA profiling of clear cell renal cell carcinoma by whole-genome small RNA deep sequencing of paired frozen and formalin-fixed, paraffin-embedded tissue specimens [J].
Weng, Lihong ;
Wu, Xiwei ;
Gao, Hanlin ;
Mu, Bing ;
Li, Xuejun ;
Wang, Jin-Hui ;
Guo, Chao ;
Jin, Jennifer M. ;
Chen, Zhuo ;
Covarrubias, Maricela ;
Yuan, Yate-Ching ;
Weiss, Lawrence M. ;
Wu, Huiqing .
JOURNAL OF PATHOLOGY, 2010, 222 (01) :41-50
[49]   miRNA profiling in metastatic renal cell carcinoma reveals a tumour-suppressor effect for miR-215 [J].
White, N. M. A. ;
Khella, H. W. Z. ;
Grigull, J. ;
Adzovic, S. ;
Youssef, Y. M. ;
Honey, R. J. ;
Stewart, R. ;
Pace, K. T. ;
Bjarnason, G. A. ;
Jewett, M. A. S. ;
Evans, A. J. ;
Gabril, M. ;
Yousef, G. M. .
BRITISH JOURNAL OF CANCER, 2011, 105 (11) :1741-1749
[50]   Identification of a 4-microRNA Signature for Clear Cell Renal Cell Carcinoma Metastasis and Prognosis [J].
Wu, Xiwei ;
Weng, Lihong ;
Li, Xuejun ;
Guo, Chao ;
Pal, Sumanta K. ;
Jin, Jennifer M. ;
Li, Yuping ;
Nelson, Rebecca A. ;
Mu, Bing ;
Onami, Susan H. ;
Wu, Jeffrey J. ;
Ruel, Nora H. ;
Wilczynski, Sharon P. ;
Gao, Hanlin ;
Covarrubias, Maricela ;
Figlin, Robert A. ;
Weiss, Lawrence M. ;
Wu, Huiqing .
PLOS ONE, 2012, 7 (05)