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JNK-mediated Ser27 phosphorylation and stabilization of SIRT1 promote growth and progression of colon cancer through deacetylation-dependent activation of Snail

Authors
 Yeon-Hwa Lee  ;  Su-Jung Kim  ;  Xizhu Fang  ;  Na-Young Song  ;  Do-Hee Kim  ;  Jinyoung Suh  ;  Hye-Kyung Na  ;  Kyung-Ok Kim  ;  Jeong-Heum Baek  ;  Young-Joon Surh 
Citation
 MOLECULAR ONCOLOGY, Vol.16(7) : 1555-1571, 2022-04 
Journal Title
MOLECULAR ONCOLOGY
ISSN
 1574-7891 
Issue Date
2022-04
MeSH
Animals ; Colonic Neoplasms* / metabolism ; Humans ; MAP Kinase Kinase 4 / metabolism* ; Mice ; Mice, Nude ; Oncogenes ; Phosphorylation ; Sirtuin 1* / genetics
Keywords
SIRT1 ; colon cancer ; deacetylation ; post-translational modification ; proinflammatory cytokines ; snail
Abstract
Sirtuin 1 (SIRT1), an NAD+ -dependent histone/protein deacetylase, has multifaceted functions in various biological events such as inflammation, aging, and energy metabolism. The role of SIRT1 in carcinogenesis, however, is still under debate. Recent studies have indicated that aberrant overexpression of SIRT1 is correlated with metastasis and poor prognosis in several types of malignancy, including colorectal cancer. In the present study, we found that both SIRT1 and SIRT1 phosphorylated on serine 27 were coordinately upregulated in colon cancer patients' tissues and human colon cancer cell lines. This prompted us to investigate a role of phospho-SIRT1 in the context of colon cancer progression. A phosphorylation-defective mutant form of SIRT1, in which serine 27 was substituted by alanine (SIRT1-S27A), exhibited lower protein stability compared to that of wild-type SIRT1. Notably, human colon cancer (HCT-116) cells harboring the SIRT1-S27A mutation showed decreased cell proliferation and reduced capability to form xenograft tumor in athymic nude mice, which was accompanied by diminished transcriptional activity of Snail. HCT-116 cells carrying SIRT1-S27A were less capable of deacetylating the Snail protein, with a concomitant decrease in the levels of interleukin (IL)-6 and IL-8 mRNA transcripts. Taken together, these observations suggest that SIRT1 stabilized through phosphorylation on serine 27 exerts oncogenic effects at least partly through deacetylation-dependent activation of Snail and subsequent transcription of IL-6 and IL-8 in human colon cancer cells.
Files in This Item:
T202201570.pdf Download
DOI
10.1002/1878-0261.13143
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
Yonsei Authors
Song, Na-Young(송나영) ORCID logo https://orcid.org/0000-0001-8658-7049
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188829
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