Journal of Southern Medical University ›› 2013, Vol. 33 ›› Issue (12): 1787-.
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Abstract: Objective To screen and identity genes related to CD133 +CD200 + colorectal cancer stem cells. Methods The twosubpopulations of colorectal cancer cells, namely CD133 +CD200 + and CD133-CD200- cells, were sorted and verified by flowcytometry. The gene expression profiles of CD133 + CD200 + and CD133-CD200- colorectal cancer cells were examined usingAffymetrix Human U133 Plus2.0 genome-wide genechip. The differentially expressed genes between the two cellsubpopulations were analyzed to identify the genes responsible for the main effect in association with colorectal cancer stemcells. Real-time quantitative PCR was performed to confirm some of the differentially expressed genes identified by genechip.Results The genechip result showed that 655 genes were differentially expressed in CD133+CD200+ colorectal cancer stem cellsby at least 3 folds, including 290 up-regulated and 365 down-regulated ones. Bioinformatics analysis and gene co-expressionnetwork building identified 3 genes (MDM2, PRKACG, and CACNA1G) with specific expression in CD133+CD200+ colorectalcancer stem cells, and this result was confirmed by real-time quantitative PCR analysis. Conclusion A specific gene expressionprofile of colorectal cancer stem cells has been established through screening and identifying genes related to CD133+CD200+colorectal cancer stem cells by gene genechip technique, which provides a basis for further study of gene targeting therapy ofcolorectal cancer.
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https://www.j-smu.com/EN/Y2013/V33/I12/1787