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Changes of expression of miR-155 in colitis-associated colonic carcinogenesis / 中华肿瘤杂志
Chinese Journal of Oncology ; (12): 257-262, 2014.
Article in Chinese | WPRIM | ID: wpr-328958
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the changes of miR-155 and its target genes in colitis-associated carcinogenesis.</p><p><b>METHODS</b>Colitis-associated colon cancer was induced by azoxymethane (AOM) and dextran sulfate sodium (DSS) in C57BL/6 mice. Mice of three different stages during the development of colon cancer were obtained, named AD1, AD2 and AD3, respectively. A control group of mice without any treatment and a DSS only group representing chronic inflammation without cancer were set up as well. Colon tissue was collected and expression of miR-155 in the colon tissues was measured by real-time fluorescent quantitative PCR. TargetScan and PicTar were used to predict potential target genes of miR-155, which were then preliminarily screened with our gene expression microarray database of AOM-DSS mouse model. Regular PCR was used to confirm the changes of the expression of these potential target genes in AOM-DSS mouse model.</p><p><b>RESULTS</b>Colitis-associated colon cancer was effectively induced by azoxymethane and dextran sulfate sodium in C57BL/6 mice. Histological examination revealed that the evolution process was sequentially from normal, mild dysplasia, moderate dysplasia, and severe dysplasia to adenocarcinoma in the AOM-DSS mouse model. The level of miR-155 was gradually elevated with the formation of colitis-associated colon cancer. There was no significant difference between the levels of miR-155 expression in the DSS group (0.005 6 ± 0.003 7) and control group (0.012 0 ± 0.005 1) (P > 0.05), but the level of miR-155 in the AD3 group (0.054 4 ± 0.027 0) was significantly higher than that of the DSS group (0.005 6 ± 0.003 7)(P < 0.01). No significant change of miR-155 expression was found in the DSS only group. The relative expression levels of miR-155 in the control group, DSS only group and AD3 group were 0.012 0 ± 0.005 1, 0.005 6 ± 0.003 7, 0.054 4 ± 0.027 0, respectively. Data analysis with the gene expression microarray showed that Tle4, Kcna1, Itk, Bcorl1, Cacna1c, Rspo2 and Foxo3 were potential target genes of miR-155 in the AOM-DSS mouse model. Changes of Kcna1 and Cacna1c in the AOM-DSS mouse model were validated to be consistent with the changes obtained with the gene expression microarray.</p><p><b>CONCLUSION</b>The up-regulation of miR-155 is related to colitis-associated carcinogenesis, but is irrelevant to chronic inflammation in the mouse model.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Precancerous Conditions / Azoxymethane / Carcinogens / Adenocarcinoma / Up-Regulation / Dextran Sulfate / Cocarcinogenesis / Colitis / Colon / Colonic Neoplasms Type of study: Prognostic study Limits: Animals Language: Chinese Journal: Chinese Journal of Oncology Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Precancerous Conditions / Azoxymethane / Carcinogens / Adenocarcinoma / Up-Regulation / Dextran Sulfate / Cocarcinogenesis / Colitis / Colon / Colonic Neoplasms Type of study: Prognostic study Limits: Animals Language: Chinese Journal: Chinese Journal of Oncology Year: 2014 Type: Article