Science Letters:IGFBP7 plays a potential tumor suppressor role against colorectal carcinogenesis with its expression associated with DNA hypomethylation of exon 1

Insulin-like growth factor binding-protein-7 (IGFBP7) was obtained from our previous colonic adenocarcinoma (CRC) and normal mucosa suppression subtraction hybridization (SSH) cDNA libraries. By RT-PCR and immunohistochemistry, we found that IGFBP7 was overexpressed in CRC tissue compared to normal...

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Published inJournal of Zhejiang University. B. Science Vol. 7; no. 11; pp. 929 - 932
Main Author RUAN Wen-jing LIN Jie XU En-ping XU Fang-ying MA Yu DENG Hong HUANG Qiong LV Bing-jian HU Hu CUI Jing DI Mei-juan DONG Jian-kang LAI Mao-de
Format Journal Article
LanguageEnglish
Published Department of Pathology, School of Medicine, Zhejiang University, Hangzhou 310031, China%Department of Pathology, School of Medicine, Zhejiang University, Hangzhou 310031, China 2006
Department of Basic Medicine, Hangzhou Teachers College, Hangzhou 310036, China%Department of Pathology, the People's No.1 Hospital of Xiaoshan, Hangzhou 311201, China) People's No.1 Hospital of Xiaoshan, Hangzhou 311201, China%Center for Disease Control and Prevention of Xiaoshan, Hangzhou 311201, China)revention of Xiaoshan, Hangzhou 311201, China
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Summary:Insulin-like growth factor binding-protein-7 (IGFBP7) was obtained from our previous colonic adenocarcinoma (CRC) and normal mucosa suppression subtraction hybridization (SSH) cDNA libraries. By RT-PCR and immunohistochemistry, we found that IGFBP7 was overexpressed in CRC tissue compared to normal tissue. However, our in vitro experiments performed in 10 CRC cell lines showed that IGFBP7 expressed only in SW480 and Caco2 cell lines, which implied an underlying reversible regulatory mechanism. Using methylation-specific PCR (MSP) and bisulfite sodium PCR (BSP), we found that its expression was associated with DNA hypomethylation of exonl. This was further supported by the in vitro study which showed restored IGFBP7 expression after demethylation agent 5-aza-2'-deoxycytidine treatment. Correlation analysis between IGFBP7 expression and prognosis indicated that overexpression of IGFBP7 in CRC tissue correlated with favourable survival. Investigation of the functional role of IGFBP7 through transfection studies showed that IGFBP7 protein could inhibit growth rate, decrease colony formation activity, and induce apoptosis in RKO and SW620 cells, suggesting it a potential tumor suppressor protein in colorectal carcinogenesis. In conclusion, our study clearly demonstrated that IGFBP7 plays a potential tumor suppressor role against colorectal carcinogenesis and its expression is associated with DNA hypomethylation of exon 1.
Bibliography:R36
33-1356/Q
IGFBP7 (Insulin-like growth factor binding-protein-7), Colorectal cancer, Tumor suppressor protein, Methylation
ISSN:1673-1581
1862-1783