SirT1 is an inhibitor of proliferation and tumor formation in colon cancer.
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| Abstract |
The NAD-dependent deacetylase SirT1 regulates factors involved in stress response and cell survival and is a potential drug target of activators and inhibitors. Determination of SirT1 function in tumor cells is important for its targeting in cancer therapy. We found that SirT1 knockdown by short hairpin RNA accelerates tumor xenograft formation by HCT116 cells, whereas SirT1 overexpression inhibits tumor formation. Furthermore, pharmacological inhibition of SirT1 stimulates cell proliferation under conditions of growth factor deprivation. Paradoxically, SirT1 inhibition also sensitizes cells to apoptosis by chemotherapy drugs. Immunohistochemical staining revealed high level SirT1 in normal colon mucosa and benign adenomas. SirT1 overexpression was observed in approximately 25% of stage I/II/III colorectal adenocarcinomas but rarely found in advanced stage IV tumors. Furthermore, approximately 30% of carcinomas showed lower than normal SirT1 expression. This pattern is consistent with SirT1 having pleiotropic effects during cancer development (anti-proliferation and anti-apoptotic). These results suggest a rationale for the use of SirT1 activators and inhibitors in the prevention and treatment of colon cancer.
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| Authors | Neha Kabra, Zhenyu Li, Lihong Chen, Baozong Li, Xiaohong Zhang, Chuangui Wang, Timothy Yeatman, Domenico Coppola, Jiandong Chen |
| Journal | The Journal of biological chemistry (J Biol Chem) Vol. 284 Issue 27 Pg. 18210-7 (Jul 03 2009) ISSN: 1083-351X [Electronic] United States |
| PMID | 19433578 (Publication Type: Journal Article, Research Support, N.I.H., Extramural) |
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