Micro-RNA profiling in kidney and bladder cancers

被引:789
作者
Gottardo, Fedra
Liu, Chang Gong
Ferracin, Manuela
Calin, George A.
Fassan, Mattect
Bassi, Pierfrancesco
Sevignani, Cinzia
Byrne, Dolores
Negrini, Massimo
Pagano, Francesco
Gomella, Leonard G. [1 ]
Croce, Carlo M.
Baffa, Raffaele
机构
[1] Thomas Jefferson Univ, Dept Urol, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Univ Padua, Dept Urol, VIMM, Padua, Italy
[3] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[5] Univ Ferrara, Microbiol Unit, Dept Expt & Diagnost Med, I-44100 Ferrara, Italy
[6] Univ Padua, Pathol Unit, Dept Diagnost Sci & Special Therapies, Padua, Italy
[7] Thomas Jefferson Univ, Kimmel Canc Ctr, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
关键词
micro-RNA; microarray; tumor marker; bladder cancer; renal cancer;
D O I
10.1016/j.urolonc.2007.01.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objectives: Micro-RNAs are a group of small noncoding RNAs with modulator activity of gene expression. Recently, micro-RNA genes were found abnormally expressed in several types of cancers. To study the role of the micro-RNAs in human kidney and bladder cancer, we analyzed the expression profile of 245 micro-RNAs in kidney and bladder primary tumors. Methods and materials: A total of 27 kidney specimens (20 carcinomas, 4 benign renal tumors, and 3 normal parenchyma) and 27 bladder specimens (25 urothelial carcinomas and 2 normal mucosa) were included in the study. Total RNA was used for hybridization on an oligonucleotide microchip for micro-RNA profiling developed in our laboratories. This microchip contains 368 probes in triplicate, corresponding to 245 human and mouse micro-RNA genes. Results: A set of 4 human micro-RNAs (miR-28, miR-185, miR-27, and let-7f-2) were found significantly up-regulated in renal cell carcinoma (P < 0.05) compared to normal kidney. Human micro-RNAs miR-223, miR-26b, miR-221, miR-103-1, miR-185, miR-23b, miR-203, miR-17-5p, miR-23a, and miR-205 were significantly up-regulated in bladder cancers (P < 0.05) compared to normal bladder mucosa. Of the kidney cancers studied, there was no differential micro-RNA expression across various stages, whereas with increasing tumor-nodes-metastasis staging in bladder cancer, miR-26b showed a moderate decreasing trend (P = 0.082). Conclusions: Our results show that different micro-RNAs are deregulated in kidney and bladder cancer, suggesting the involvement of these genes in the development and progression of these malignancies. Further studies are needed to clarify the role of micro-RNAs in neoplastic transformation and to test the potential clinical usefulness of micro-RNAs microarrays as diagnostic and prognostic tool. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:387 / 392
页数:6
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