Activation of the LINC00242/miR-141/FOXC1 axis underpins the development of gastric cancer

• Published in: Cancer cell international Vol. 20; no. 1; pp. 272 - 11
• Main Authors: Zhong, Xiongdong, Yu, Xianchang, Wen, Xiaoyan, Chen, Lei, Gu, Ni
• Format: Journal Article
• Language: English
• Published: England BioMed Central 24.06.2020; BMC
• Subjects: Angiogenesis; Binding sites; Biotechnology; Cancer therapies; Carcinogenesis; Cell culture; Cell growth; Cell migration; Cell viability; Chemotherapy; Cholecystokinin; Endothelial cells; Fluorides; FOXC1; Gastric cancer; Gene expression; Immunoprecipitation; Laboratory animals; LINC00242; Localization; Metastasis; MicroRNA-141; MicroRNAs; Microvasculature; Non-coding RNA; Primary Research; Radiation therapy; Reporter gene; Ribonucleic acid; RNA; Xenografts; Beijing China; United States > US; China; FOXC1; LINC00242; MicroRNA-141; Gastric cancer
• ISSN: 1475-2867; 1475-2867
• DOI: 10.1186/s12935-020-01369-7

Long non-coding RNAs (LncRNAs) are a class of newly identified transcripts recognized as critical governors of gene expression during human carcinogenesis, whereas their tumor-suppressive or tumor-promoting effects on gastric cancer (GC) are required for further investigation. In the study, we identify the expression pattern of a novel lncRNA LINC00242 in GC and its possible permissive role in the development of GC. The study included 68 pairs of GC and adjacent normal gastric tissue samples. The viability, migration, and invasion of cultured human GC cells HGC27 were evaluated by CCK-8 and Transwell chamber assays. In vitro tube formation of human brain microvascular endothelial cells (HBMVECs) in HGC27 cell coculture was detected. The regulatory network of LINC00242/miR-141/FOXC1 was verified using dual luciferase reporter gene assay and RNA immunoprecipitation (RIP) assay. Subcutaneous xenografts of HGC27 cells were performed in nude mice. LINC00242 was highly expressed in GC tissues and cells and contributed to poor prognosis. LINC00242 knockdown inhibited HGC27 cell viability, migration and invasion, and tube formation of HBMVECs. LINC00242 interacted with miR-141 and positively regulated FOXC1, a target gene of miR-141. LINC00242 knockdown was partially lost in HGC27 cells upon miR-141 inhibition or FOXC1 overexpression. The tumor-promoting effect of LINC00242 on GC was demonstrated in nude mice. Taken together, the present study demonstrates the oncogenic role of the LINC00242/miR-141/FOXC1 axis in GC, highlighting a theoretical basis for GC treatment.