[No authors listed]
The aim of the present study was to investigate the role of miRâ203aâ3p in colorectal cancer (CRC) and identify the target gene of microRNA (miR)â203aâ3p. A total of 59 sets of cancer tissues and corresponding adjacent nonâtumor tissues were collected from CRC patients (aged 31â78 years) between October 2016 and May 2017. Total RNA extraction and reverse transcriptionâquantitative polymerase chain reaction analysis, transfection assay, and Transwell and apoptosis assays, western blot analysis, a luciferase reporter assay and immunohistochemistry were performed. miRâ203aâ3p was found to be significantly downregulated in CRC tissues compared with adjacent normal tissues. The overexpression of miRâ203aâ3p was shown to inhibit the invasion and migration of human CRC SW480 and HT29 cells, and increase their apoptosis rates. Furthermore, miRâ203aâ3p downregulated the expression of thrombospondin 2 (THBS2) in SW480 and HT29 cells. It was also experimentally demonstrated that miRâ203aâ3p binds to the 3'âuntranslated region of THBS2, downregulating THBS2 expression and thereby inhibiting CRC progression and metastasis. The expression of miRâ203aâ3p, which serves a tumorâsuppressive role, in CRC tissues was significantly downregulated. As miRâ203aâ3p was determined to target THBS2 to inhibit CRC progression and metastasis; thus, miRâ203aâ3p may be considered as a potential novel approach to treating CRC.
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