LINC00294/miR-620/MKRN2 axis provides biomarkers and negatively regulates malignant progression in colorectal carcinoma

• Published in: Human & experimental toxicology 2023-03, Vol.42, p.9603271231167577-9603271231167577
• Main Authors: Qi, Puliang, Yexie, Zhihua, Xue, Chen, Huang, Guoqiang, Zhao, Zhanxue, Zhang, Xikun
• Format: Article
• Language: English
• Subjects: Bioinformatics; Biomarkers; Cell Line, Tumor; Cell migration; Cell Movement - genetics; Cell proliferation; Cell Proliferation - genetics; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - metabolism; Comparative analysis; Gene Expression Regulation, Neoplastic; Humans; Malignancy; MicroRNAs - genetics; MicroRNAs - metabolism; Non-coding RNA; Prognosis; Rank tests; Ribonucleoproteins - genetics; Ribonucleoproteins - metabolism; Survival; Tumor suppressor genes; Zinc finger proteins
• ISSN: 0960-3271; 1477-0903
• DOI: 10.1177/09603271231167577

Background Colorectal carcinoma (CRC) ranks the third most frequent malignancy worldwide. Makorin RING zinc finger-2 (MKRN2) has been identified as a tumor suppressor in CRC, and the bioinformatics prediction indicated that some non-coding RNAs (ncRNAs) that directly or indirectly regulate MKRN2 might play critical roles in CRC progression. This study aimed to analyze the regulatory effect of LINC00294 on CRC progression, and to explore the underlying mechanisms by assessing miR-620 and MKRN2. The potential prognostic value of the ncRNAs and MKRN2 was also investigated. Methods The expression of LINC00294, MKRN2, miR-620 was examined by qRT-PCR. Cell counting kit-8 assay was used to assess the proliferation of CRC cells. Transwell assay was used to evaluate the migration, invasion of CRC cells. Kaplan-Meier method and log-rank test were used to perform comparative analysis of overall survival in CRC patients. Results Lower expression of LINC00294 was observed in both CRC tissues and cell lines. In CRC cells, LINC00294 overexpression inhibited cell proliferation, migration and invasion, but these effects were directly reversed by the overexpression of miR-620, which was demonstrated as a target of LINC00294. Additionally, MKRN2 was found to be a target gene of miR-620, and might mediate the regulatory function of LINC00294 in CRC progression. In CRC patients, low LINC00294, MKRN2 and high miR-620 expression was associated poor overall survival of CRC. Conclusions LINC00294/miR-620/MKRN2 axis had the potential to provide prognostic biomarkers for CRC patients, and negatively regulated the malignant progression of CRC cells, including proliferation, migration and invasion.