SIRT1 and the Clock Gene Machinery in Colorectal Cancer

被引:17
|
作者
Pazienza, Valerio [3 ,4 ]
Piepoli, Ada [3 ,4 ]
Panza, Anna [3 ,4 ]
Valvano, Maria Rosa [3 ,4 ]
Benegiamo, Giorgia [3 ,4 ]
Vinciguerra, Manlio [5 ,6 ]
Andriulli, Angelo [3 ,4 ]
Mazzoccoli, Gianluigi [1 ,2 ]
机构
[1] Res Hosp, Div Internal Med, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, FG, Italy
[2] Res Hosp, Chronobiol Unit, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, FG, Italy
[3] Res Hosp, Div Gastroenterol, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, FG, Italy
[4] Res Hosp, Lab Gastroenterol, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, FG, Italy
[5] Ist EuroMEditerraneo Sci & Tecnol, Palermo, Italy
[6] Univ London Birkbeck Coll, Inst Hepatol, London WC1E 7HX, England
关键词
SIRT1; Clock genes; Colorectal cancer; CIRCADIAN CLOCK; TUMOR SUPPRESSION; COLON-CANCER; CHK2; ACTIVATION; GROWTH; EXPRESSION; INHIBITOR; P53; PROLIFERATION; SENESCENCE;
D O I
10.3109/07357907.2011.640650
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
SIRT1 and the clock genes are involved in carcinogenesis. We evaluated SIRT1 expression in 19 human colorectal cancer (CRC) specimens and clock gene expression in SIRT1-overexpressing CaCo2 and SW480 cells. In CRC, SIRT1 mean expression level was decreased. Compared to CaCo2 cells, SW480 cells displayed lower levels of SIRT1 and PER3 and higher levels of ARNTL1, CLOCK, PER1, PER2, CRY1, TIPIN, and CSNKIE. SIRT1 overexpression induced PER1 upregulation in CaCo2 and downregulation in SW480 cells. SIRT1 expression was heterogeneous in human CRC and in CRC cell lines. These results might have relevant implications for a better understanding of colorectal carcinogenesis.
引用
收藏
页码:98 / 105
页数:8
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