2020BioMed Research InternationalOpen access

Long Noncoding RNA MALAT1 Promotes Colorectal Cancer Progression by Acting as a ceRNA of miR‐508‐5p to Regulate RAB14 Expression

Chen Zhang, Kunhou Yao, Junjie Zhang, Chenyu Wang, Chaoyang Wang, Changjiang Qin

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Abstract

Accumulating evidence suggested that lncRNA MALAT1 plays critical roles in the commencement and progression of malignant cancers. Nevertheless, the function of MALAT1 in colorectal cancer (CRC) remains largely unknown. In the present study, we reported that MALAT1 expression is significantly upregulated in CRC and correlated with advanced TNM stage, lymph node metastasis, and worse prognosis in patients. Functional assays revealed that MALAT1 knockdown reduced CRC cell growth and invasion abilities in vitro. Mechanistically, we discovered that MALAT1 may serve as a competing endogenous RNA (ceRNA) to miR‐508‐5p in CRC progression. Bioinformatics analysis and luciferase assays confirmed that RAB14 acts as a target of miR‐508‐5p. In addition, downregulation of RAB14 reduced the progression of CRC. Collectively, our findings indicated that MALAT1 could promote CRC progress by sponging miR‐508‐5p and enhancing RAB14 expression, which provides a therapeutic target in CRC treatment.

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What this paper is about

Accumulating evidence suggested that lncRNA MALAT1 plays critical roles in the commencement and progression of malignant cancers. Nevertheless, the function of MALAT1 in colorectal cancer (CRC) remains largely unknown. In the present study, we reported that MALAT1 expression is significantly upregulated in CRC and correlated with advanced TNM stage, lymph node metastasis, and worse prognosis in patients. Functional assays revealed that MALAT1 knockdown reduced CRC cell growth and invasion abilities in vitro. Mechanistically, we discovered that MALAT1 may serve as a competing endogenous RNA (ceRNA) to miR‐508‐5p in CRC progression. Bioinformatics analysis and luciferase assays confirmed that RAB14 acts as a target of miR‐508‐5p. In addition, downregulation of RAB14 reduced the progression of CRC. Collectively, our findings indicated that MALAT1 could promote CRC progress by sponging miR‐508‐5p and enhancing RAB14 expression, which provides a therapeutic target in CRC treatment.

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Available abstract

Accumulating evidence suggested that lncRNA MALAT1 plays critical roles in the commencement and progression of malignant cancers. Nevertheless, the function of MALAT1 in colorectal cancer (CRC) remains largely unknown. In the present study, we reported that MALAT1 expression is significantly upregulated in CRC and correlated with advanced TNM stage, lymph node metastasis, and worse prognosis in patients. Functional assays revealed that MALAT1 knockdown reduced CRC cell growth and invasion abilities in vitro. Mechanistically, we discovered that MALAT1 may serve as a competing endogenous RNA (ceRNA) to miR‐508‐5p in CRC progression. Bioinformatics analysis and luciferase assays confirmed that RAB14 acts as a target of miR‐508‐5p. In addition, downregulation of RAB14 reduced the progression of CRC. Collectively, our findings indicated that MALAT1 could promote CRC progress by sponging miR‐508‐5p and enhancing RAB14 expression, which provides a therapeutic target in CRC treatment.

Key concepts: MALAT1, Competing endogenous RNA, Long non-coding RNA, microRNA, Biology, Colorectal cancer, Cancer research, RNA

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Long Noncoding RNA MALAT1 Promotes Colorectal Cancer Progression by Acting as a ceRNA of miR‐508‐5p to Regulate RAB14 Expression — Research Paper | ScholarLens