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    To investigate the expression of receptor-tyrosine-kinase-like orphan receptor 1 (ROR1) and its role in cell growth in human colorectal carcinoma (CRC). Real-time quantitative PCR (qRT-PCR) and immunohistochemistry (IHC) were used to detect the expression of ROR1 in CRC (n=60) and matched tumor-adjacent tissues. The relationship between the expression of ROR1 and clinical features was analyzed by Pearson chi-square test. siRNA was used to down-regulate the expression of ROR1 in SW480 cells in vitro. The qRT-PCR and Western blotting were performed to confirm the down-regulation of ROR1 expression. The effects of down-regulated ROR1 on cell proliferation and apoptosis were measured by MTT assay and flow cytometry combined with annexin V-FITC/PI staining, respectively. Both the mRNA and protein expression of ROR1 were significantly up-regulated in CRC tissues than in tumor-adjacent tissues, and the expression of ROR1 was positively correlated with tumor size (≥5 cm), lymphatic metastasis and TNM stage (III and IV). siRNA could significantly down-regulate the expression of ROR1 in SW480 cells, then suppressed proliferation and enhanced apoptosis in SW480 cells. The expression of ROR1 was significantly higher in CRC tissues than in tumor-adjacent tissues. Down-regulation of ROR1 could play an anti-cancer role through inhibiting proliferation and inducing apoptosis in CRC.

    Citation

    Wenqi Ma, Xin He, Hongli Zhang, Ting Liu, Xiaolei Feng, Qi Zhou. Down-regulation of receptor-tyrosine-kinase-like orphan receptor 1 suppresses cell growth and enhances apoptosis in human colorectal carcinoma]. Xi bao yu fen zi mian yi xue za zhi = Chinese journal of cellular and molecular immunology. 2016 May;32(5):655-9, 665

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    PMID: 27126945

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