Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues

被引:713
作者
Bandres, E. [1 ]
Cubedo, E.
Agirre, X.
Malumbres, R.
Zarate, R.
Ramirez, N.
Abajo, A.
Navarro, A.
Moreno, I.
Monzo, M.
Garcia-Foncillas, J.
机构
[1] Univ Navarra, Lab Pharmacogenom, Canc Res Program, Ctr Appl Med Res, Navarra, Spain
[2] Univ Navarra, Div Canc & Area Cell Therapy, Navarra, Spain
[3] Univ Navarra, Hematol Serv, Ctr Appl Med Res, Navarra, Spain
[4] Univ Barcelona, Fac Med, Dept Human Anat, Barcelona, Spain
[5] Hosp Municipal Badalona, Dept Med Oncol, Badalona, Spain
关键词
D O I
10.1186/1476-4598-5-29
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs ( miRNAs) are short non-coding RNA molecules playing regulatory roles by repressing translation or cleaving RNA transcripts. Although the number of verified human miRNA is still expanding, only few have been functionally described. However, emerging evidences suggest the potential involvement of altered regulation of miRNA in pathogenesis of cancers and these genes are thought to function as both tumours suppressor and oncogenes. In our study, we examined by Real-Time PCR the expression of 156 mature miRNA in colorectal cancer. The analysis by several bioinformatics algorithms of colorectal tumours and adjacent nonneoplastic tissues from patients and colorectal cancer cell lines allowed identifying a group of 13 miRNA whose expression is significantly altered in this tumor. The most significantly deregulated miRNA being miR-31, miR-96, miR-133b, miR-135b, miR-145, and miR-183. In addition, the expression level of miR-31 was correlated with the stage of CRC tumor. Our results suggest that miRNA expression profile could have relevance to the biological and clinical behavior of colorectal neoplasia.
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