Tumour-promoting role of SOCS1 in colorectal cancer cells

被引:30
作者
Tobelaim, William S. [1 ]
Beaurivage, Claudia [1 ]
Champagne, Audrey [1 ]
Pomerleau, Veronique [1 ]
Simoneau, Aline [1 ]
Chababi, Walid [1 ]
Yeganeh, Mehdi [2 ,3 ]
Thibault, Philippe [4 ]
Klinck, Roscoe [4 ]
Carrier, Julie C. [1 ]
Ferbeyre, Gerardo [5 ]
Ilangumaran, Subburaj [2 ,3 ]
Saucier, Caroline [1 ]
机构
[1] Univ Sherbrooke, Fac Med & Hlth Sci, Dept Anat & Cell Biol, Sherbrooke, PQ J1E 4K8, Canada
[2] Univ Sherbrooke, Fac Med & Hlth Sci, Dept Pediat, Sherbrooke, PQ J1E 4K8, Canada
[3] Univ Sherbrooke, Fac Med & Hlth Sci, Div Immunol, Sherbrooke, PQ J1E 4K8, Canada
[4] Univ Sherbrooke, Fac Med & Hlth Sci, Dept Microbiol & Infectiol, Sherbrooke, PQ J1E 4K8, Canada
[5] Univ Montreal, Dept Biochem, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
ISLAND METHYLATOR PHENOTYPE; MET RECEPTOR; NEGATIVE REGULATOR; ANTITUMOR-ACTIVITY; EPITHELIAL-CELLS; GENE-EXPRESSION; GROWTH; SUPPRESSION; PROGRESSION; STAT3;
D O I
10.1038/srep14301
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The SOCS1 (Suppressor Of Cytokine Signalling 1) protein is considered a tumour suppressor. Notably, the SOCS1 gene is frequently silenced in cancer by hypermethylation of its promoter. Besides blocking inflammation, SOCS1 tumour suppressor activity involves Met receptor inhibition and enhancement of p53 tumour suppressor activity. However, the role of SOCS1 in colorectal cancer (CRC) remains understudied and controversial. Here, we investigated SOCS1 relevance for CRC by querying gene expression datasets of human CRC specimens from The Cancer Genome Atlas (TCGA), and by SOCS1 gain/loss-of-function analyses in murine and human colon carcinoma cells. Our results show that SOCS1 mRNA levels in tumours were more often elevated than reduced with respect to matched adjacent normal tissue of CRC specimens (n = 41). The analysis of TCGA dataset of 431 CRC patients revealed no correlation between SOCS1 expression and overall survival. Overexpression of SOCS1 in CRC cells triggered cell growth enhancement, anchorage-independent growth and resistance to death stimuli, whereas knockdown of SOCS1 reduced these oncogenic features. Moreover, SOCS1 overexpression in mouse CT26 cells increased tumourigenesis in vivo. Biochemical analyses showed that SOCS1 pro-oncogenic activity correlated with the down-modulation of STAT1 expression. Collectively, these results suggest that SOCS1 may work as an oncogene in CRC.
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页数:13
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