Long noncoding RNA KCNMA1-AS2 regulates the function of colorectal cancer cells and sponges miR-1227-5p

被引:0
作者
Miao, Xinzhi [1 ,2 ,3 ]
Wang, Fang [2 ,3 ,4 ]
Yunus, Muhammad Amir [2 ]
Ismail, Ida Shazrina [2 ]
Wang, Tianyun [3 ]
机构
[1] Xinxiang Med Univ, Sch Med Humanities, Xinxiang 453003, Henan, Peoples R China
[2] Univ Sains Malaysia, Adv Med & Dent Inst, Dept Biomed Sci, Kepala Batas 13200, Penang, Malaysia
[3] Xinxiang Med Univ, Henan Int Joint Lab Recombinant Pharmaceut Prot Ex, Xinxiang 453003, Henan, Peoples R China
[4] Xinxiang Med Univ, Dept Biochem & Mol Biol, Xinxiang 453003, Henan, Peoples R China
关键词
KCNMA1-AS2; Biomarker; Colorectal cancer; miR-1227-5p; Long noncoding RNA; HYPERMETHYLATION; PROLIFERATION; CYCLE;
D O I
10.1186/s12885-024-12608-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundMany long noncoding RNAs (lncRNAs) with altered expression significantly influence colorectal cancer (CRC) progression and behavior. The functions of many lncRNAs in CRC are not clear yet. This study aimed to discover novel lncRNA entities and comprehensively examine and validate their roles and underlying molecular mechanisms in CRC.MethodsTissue samples, both tumourous and non-tumourous, from three CRC patients were submitted for sequencing. Following expression validation in samples from ten patients and four CRC cell lines. The lncRNA KCNMA1-AS2 was synthesized by In-vitro transcription RNA synthesis and the lncRNA was directly transfected into CRC cell lines to overexpress. Functional assays including MTT proliferation assay, Annexin-V/propidium iodide apoptosis assay, wound healing migration assay and cell cycle assays were performed to evaluate the effect of overexpression of KCNMA1-AS2. Furthermore, the binding of KCNMA1-AS2 to miR-1227-5p was confirmed using dual luciferase reporter assays and qPCR analyses. Subsequent bioinformatics analyses identified 58 potential downstream targets of miR-1227-5p across three databases.ResultsIn this study, we identified the lncRNA KCNMA1-AS2, the expression of which was down-regulated consistently in cancer tissues and CRC cell lines compared to non-cancerous tissues. The overexpression of lncRNA KCNMA1-AS2 led to significant reduction in CRC cell proliferation and migration, increase in cell apoptosis, and more cells arrested in S phase. Additionally, the interaction between KCNMA1-AS2 and miR-1227-5p was confirmed through dual luciferase reporter assay and qPCR analysis. It is also putatively predicted that MTHFR and ST8SIA2 may be linked to CRC based on bioinformatics analyses.ConclusionsLncRNA KCNMA1-AS2 exhibited distinct gene expression patterns in both CRC tissue and cell lines, impacting various cellular functions while also acting as a sponge for miR-1227-5p.The findings spotlight lncRNA KCNMA1-AS2 as a potential marker for diagnosis and treatment of CRC.
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页数:12
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