Epigenetic regulation of microRNA expression in colorectal cancer

被引:361
|
作者
Bandres, Eva [1 ]
Agirre, Xabier [2 ,3 ]
Bitarte, Nerea [1 ]
Ramirez, Natalia [1 ]
Zarate, Ruth [1 ]
Roman-Gomez, Jose [4 ]
Prosper, Felipe [2 ,3 ]
Garcia-Foncillas, Jesus [1 ]
机构
[1] Univ Navarra, Lab Pharmacogen, Div Oncol, Ctr Appl Med Res CIMA, Pamplona 31008, Navarra, Spain
[2] Univ Navarra, Div Oncol, Dept Hematol Serv, Ctr Appl Med Res CIMA, Navarra, Spain
[3] Univ Navarra, Area Cell Therapy, Ctr Appl Med Res CIMA, Navarra, Spain
[4] Reina Sofia Hosp, Dept Hematol, Cordoba, Spain
关键词
microrna; epigenetic; colon; metastasis; DNA METHYLATION; BREAST-CANCER; CELLS; HYPERMETHYLATION; DIFFERENTIATION; ACTIVATION; PROFILES; TARGETS; GENES; PCR;
D O I
10.1002/ijc.24638
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the last years, microRNAs (miRNA) have emerged as new molecular players involved in carcinogenesis. Deregulation of miRNAs expression has been shown in different human cancer but the molecular mechanism underlying the alteration of miRNA expression is unknown. To identify tumor-supressor miRNAs silenced through aberrant epigenetic events in colorectal cancer (CRC), we used a sequential approach. We first identified 5 miR-NAs down-regulated in patient with colorectal cancer samples and located around/on a CpG island. Treatment with a DNA methyltransferase inhibitor and a HDAC inhibitor restored expression of 3 of the 5 microRNAs (hsa-miR-9, hsa-miR-129 and hsa-miR-137) in 3 CRC cell lines. Expression of hsa-miR-9 was inversely correlated with methylation of their promoter regions as measure by MSP and bisulphate sequencing. Further, methylation of the hsa-miR-9-1, hsa-miR-129-2 and hsa-miR-137 CpG islands were frequently observed in CRC cell lines and in primary CRC tumors, but not in normal colonic mucosa. Finally, methylation of hsa-miR-9-1 was associated with the presence of lymph node metastasis. In summary, our results aid in the understanding of miRNA gene regulation showing that aberrant DNA methylation and histone modifications work together to induce silencing of miRNAs in CRC. (C) 2009 UICC
引用
收藏
页码:2737 / 2743
页数:7
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