Comprehensive silencing of target-sharing microRNAs is a mechanism for SIRT1 overexpression in cancer.

Autor: Kiga K; a Max-Planck-Institute of Immunobiology and Epigenetics ; Freiburg , Germany., Fukuda-Yuzawa Y, Tanabe M, Tsuji S, Sasakawa C, Fukao T
Jazyk: angličtina
Zdroj: RNA biology [RNA Biol] 2014; Vol. 11 (11), pp. 1347-54.
DOI: 10.4161/rna.32093
Abstrakt: Overexpression of SIRT1 is frequently observed in various types of cancers, suggesting its potential role in malignancies. However, the molecular basis of how SIRT1 is elevated in cancer is less understood. Here we show that cancer-related SIRT1 overexpression is due to evasion of Sirt1 mRNA from repression by a group of Sirt1-targeting microRNAs (miRNAs) that might be robustly silenced in cancer. Our comprehensive library-based screening and subsequent miRNA gene profiling revealed a housekeeping gene-like broad expression pattern and strong CpG island-association of the Sirt1-targeting miRNA genes. This suggests aberrant CpG DNA methylation as the mechanistic background for malignant SIRT1 elevation. Our work also provides an example where epigenetic mechanisms cause the group-wide regulation of miRNAs sharing a common key target.
Databáze: MEDLINE