[No authors listed]
Colorectal cancer (CRC) currently leads to many deaths worldwide. The regulatory mechanism, however, remains largely unclear. In the present study, bioinformatics methods were used to identify genes associated with CRC prognosis and to detect the molecular signals regulating the cell cycle in two CRC cell lines. It was revealed that BNIPLâ2 expression was higher in CRC tissues than in adjacent tissue samples. Upregulation of BNIPLâ2 was correlated with poor prognosis and the adverse malignant stages T and M. BNIPLâ2 was also associated with signaling pathways involved in cancer cell growth. BNIPLâ2 overexpression promoted cell proliferation and increased the proportion of cells in the G2/M phase. Knockdown of BNIPLâ2 inhibited cell proliferation. CD44 was regulated by BNIPLâ2 and promoted cell proliferation. Downregulation of CD44 suppressed cell proliferation and rescued the cell proliferation promoted by BNIPLâ2. Overexpression of CD44 restored the cell proliferation suppressed by BNIPLâ2 knockdown. The present study not only suggested that BNIPLâ2 may be a potential biomarker of CRC but also indicated that BNIPLâ2 regulates CRC cancer proliferation via CD44, which could be a diagnostic and clinical treatment target.
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