| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Reviews |
1 Children's Cancer Institute Australia for Medical Research and 2 Centre for Children's Cancer and Blood Disorders, Sydney Children's Hospital, Randwick, Sydney, New South Wales, Australia
Requests for reprints: Glenn M. Marshall, Centre for Children's Cancer and Blood Disorders, Sydney Children's Hospital, High Street, Randwick, Sydney, NSW 2031, Australia. Phone: 61-2-93821721; Fax: 61-2-93821789; E-mail: g.marshall{at}unsw.edu.au.
Key Words: SIRT1 deacetylation methylation tumorigenesis experimental therapy
Gene expression and deacetylase activity of the class III histone deacetylase SIRT1 are up-regulated in cancer cells due to oncogene overexpression or loss of function of tumor suppressor genes. SIRT1 induces histone deacetylation and methylation, promoter CpG island methylation, transcriptional repression, and deacetylation of tumor suppressor proteins. SIRT1 may play a critical role in tumor initiation, progression, and drug resistance by blocking senescence and apoptosis, and promoting cell growth and angiogenesis. SIRT1 inhibitors have shown promising anticancer effects in animal models of cancer. Further screening for more potent SIRT1 inhibitors may lead to compounds suitable for clinical trials in patients. [Cancer Res 2009;69(5):1702–5]
This article has been cited by other articles:
![]() |
N. VALERI, C. M. CROCE, and M. FABBRI Pathogenetic and Clinical Relevance of MicroRNAs in Colorectal Cancer Cancer Genomics Proteomics, July 1, 2009; 6(4): 195 - 204. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. S. Schrump Cytotoxicity Mediated by Histone Deacetylase Inhibitors in Cancer Cells: Mechanisms and Potential Clinical Implications Clin. Cancer Res., June 15, 2009; 15(12): 3947 - 3957. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |