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miR-124 regulates radiosensitivity of colorectal cancer cells by targeting PRRX1 / 南方医科大学学报
Article in Zh | WPRIM | ID: wpr-286838
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To detect the expression of miR-124 in colorectal carcinoma (CRC) cells and tissue specimens and analyze its association with the radiosensitivity of the cells.</p><p><b>METHODS</b>The expression of miR-124 in CRC cell lines and tissues were detected using qRT-PCR. The effect of miR-124 in modulating cell radiosensitivity was assessed in CRC cells with miRNA-124 overexpression and miRNA-124 knockdown, and bioinformatics prediction and dual luciferase reporter system were employed to identify the direct target of miR-124.</p><p><b>RESULTS</b>s miR-124 expression was down-regulated in CRC cell lines and tissues. CRC cells over-expressing miR-124 showed an obviously enhanced radiosensitivity, whereas miR-124 knockdown resulted in a reduced radiosensitivity of the cells. Bioinformatics prediction and dual luciferase reporter system verified PRRX1 as a direct target of miR-124, which regulated the radiosensitivity of CRC cells by directly inhibiting PRRX1.</p><p><b>CONCLUSION</b>miR-124 can enhance the radiosensitivity of CRC cells by directly targeting PRRX1, which provides a target for improving the therapeutic effect of radiotherapy of CRC.</p>
Subject(s)
Full text: 1 Database: WPRIM Main subject: Pathology / Radiation Tolerance / Radiotherapy / Colorectal Neoplasms / Down-Regulation / Gene Expression Regulation, Neoplastic / Homeodomain Proteins / MicroRNAs / Cell Line, Tumor / Genetics Limits: Humans Language: Zh Journal: Journal of Southern Medical University Year: 2016 Document type: Article
Full text: 1 Database: WPRIM Main subject: Pathology / Radiation Tolerance / Radiotherapy / Colorectal Neoplasms / Down-Regulation / Gene Expression Regulation, Neoplastic / Homeodomain Proteins / MicroRNAs / Cell Line, Tumor / Genetics Limits: Humans Language: Zh Journal: Journal of Southern Medical University Year: 2016 Document type: Article