下调和上调
基因敲除
结直肠癌
CD44细胞
癌症研究
癌基因
生物
癌症
细胞周期
分子医学
细胞生长
癌症干细胞
细胞
转移
癌变
结直肠癌中缺失
免疫组织化学
细胞凋亡
医学
内科学
基因
遗传学
作者
Lei Gao,Hansong Liu,Ningwei Yin,Shanshan Zuo,Guangli Jin,Yang-Xi Hu,Desheng Hu,Ying Liu,Qibin Song,Xuejie Fei
标识
DOI:10.3892/mmr.2019.10633
摘要
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 BNIPL‑2 expression was higher in CRC tissues than in adjacent tissue samples. Upregulation of BNIPL‑2 was correlated with poor prognosis and the adverse malignant stages T and M. BNIPL‑2 was also associated with signaling pathways involved in cancer cell growth. BNIPL‑2 overexpression promoted cell proliferation and increased the proportion of cells in the G2/M phase. Knockdown of BNIPL‑2 inhibited cell proliferation. CD44 was regulated by BNIPL‑2 and promoted cell proliferation. Downregulation of CD44 suppressed cell proliferation and rescued the cell proliferation promoted by BNIPL‑2. Overexpression of CD44 restored the cell proliferation suppressed by BNIPL‑2 knockdown. The present study not only suggested that BNIPL‑2 may be a potential biomarker of CRC but also indicated that BNIPL‑2 regulates CRC cancer proliferation via CD44, which could be a diagnostic and clinical treatment target.
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