Inactivation of miR-34a by aberrant CpG methylation in multiple types of cancer
Max Planck Institute of Biochemistry · Max Planck Society
Abstract
Recently, we and others identified the microRNA miR-34a as a target of the tumor suppressor gene product p53. Ectopic miR-34a induces a G(1) cell cycle arrest, senescence and apoptosis. Here we report that miR-34a expression is silenced in several types of cancer due to aberrant CpG methylation of its promoter. 19 out of 24 (79.1%) primary prostate carcinomas displayed CpG methylation of the miR-34a promoter and concomitant loss of miR-34a expression. CpG methylation of the miR-34a promoter was also detected in breast (6/24; 25%), lung (7/24; 29.1%), colon (3/23; 13%), kidney (3/14; 21.4%), bladder (2/6; 33.3%) and pancreatic (3/19; 15.7%) carcinoma cell lines, as well as in melanoma cell lines (19/44; 43.2%)…
Citation impact
- FWCI
- 23.86
- Percentile
- 100%
- References
- 30
Authors
9- DLDmitri LodyginCorresponding
Max Planck Institute of Biochemistry
- VTValery Tarasov
Max Planck Society, Max Planck Institute of Biochemistry
- AEAlexey Epanchintsev
Max Planck Society, Max Planck Institute of Biochemistry
- CBCarola Berking
- TKTatjana Knyazeva
Max Planck Society, Max Planck Institute of Biochemistry
Topics & keywords
- Biology
- Cancer research
- DNA methylation
- Gene silencing
- Ectopic expression
- CpG site
- Transactivation
- microRNA
- Good health and well-being