4.3 Review

Epigenetic regulation of kallikrein-related peptidases: there is a whole new world out there

Journal

BIOLOGICAL CHEMISTRY
Volume 393, Issue 5, Pages 319-330

Publisher

WALTER DE GRUYTER & CO
DOI: 10.1515/hsz-2011-0273

Keywords

cancer; epigenetic; histone; kallikrein; methylation; miRNA

Funding

  1. Canadian Cancer Society (CCS) [20185]
  2. Ministry of Research and Innovation of the Government of Ontario
  3. Kidney Foundation of Canada
  4. Canadian Institute of Health Research (CIHR MOP) [97733]
  5. University of Toronto
  6. Ontario Student Opportunity Trust

Ask authors/readers for more resources

The human kallikreins are a cluster of 15 kallikreins and kallikrein-related peptidases (KLKs). Evidence shows the involvement of KLKs in a wide range of pathophysiological processes, and underscores their potential contribution to cancer, skin and neurodegenerative disorders. The control of KLK expression is not fully elucidated. Understanding the mechanisms controlling KLK expression is an essential step towards exploring the pathogenesis of several diseases and the use of KLKs as disease biomarkers and/or therapeutic targets. Recently, epigenetic changes (including methylation, histone modification and microRNAs [miRNAs]) have drawn attention as a new dimension for controlling KLK expression. Reports showed the effect of methylation on the expression of KLK genes. This was also shown to have potential utility as a prognostic marker in cancer. miRNAs are small RNAs that control the expression of their targets at the post-transcriptional level. Target prediction showed that KLKs are potential targets of miRNAs that are dysregulated in tumors, including prostate, kidney and ovarian cancers, with downstream effect on tumor proliferation. Experimental validation remains an essential step to confirm the KLK-miRNA interaction. Epigenetic regulation of KLKs holds promise for an array of therapeutic applications in many diseases including cancer.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available