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SLCO4A1‐AS1 promotes cell growth and induces resistance in lung adenocarcinoma by modulating miR‐4701‐5p/NFE2L1 axis to activate WNT pathway

Long noncoding RNAs (lncRNAs) possessed essential functions in the biological behaviors of various human cancers. SLCO4A1 antisense RNA 1 (SLCO4A1‐AS1) is a lncRNA that has been reported as a oncogenic regulator in colorectal cancer and bladder cancer. However, whether it exerted functions in the ge...

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Detalles Bibliográficos
Autores principales: Wei, Yuxuan, Wei, Li, Li, Jiwei, Ma, Zeheng, Zhang, Quan, Han, Zhijun, Li, Saisai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541149/
https://www.ncbi.nlm.nih.gov/pubmed/32762035
http://dx.doi.org/10.1002/cam4.3270
Descripción
Sumario:Long noncoding RNAs (lncRNAs) possessed essential functions in the biological behaviors of various human cancers. SLCO4A1 antisense RNA 1 (SLCO4A1‐AS1) is a lncRNA that has been reported as a oncogenic regulator in colorectal cancer and bladder cancer. However, whether it exerted functions in the gene expression and cellular processes in lung adenocarcinoma (LUAD) remains still obscure. In the present research, we unveiled the high level of SLCO4A1‐AS1 in LUAD tissues and cells. Moreover, functional assays indicated that SLCO4A‐AS1 facilitated LUAD cell proliferation, motility, and cisplatin‐resistance. Besides, mechanism investigation revealed that miR‐4701‐5p could interact with SLCO4A1‐AS1 and directly target to NFE2L1. The expression correlation between miR‐4701‐5p and SLCO4A1‐AS1 or NFE2L1 was found to be negative. Moreover, NFE2L1 was expressed at a same tendency with SLCO4A1‐AS1 in LUAD tissues and cells. In addition, it was confirmed that NFE2L1 was involved in SLCO4A1‐AS1‐mediated activation of WNT pathway. According to rescue assays, NFE2L1 could involve in SLCO4A1‐AS1‐mediated LUAD cell growth. Conclusively, our study demonstrated that SLCO4A1‐AS1 facilitated cell growth and enhanced the resistance of LUAD cells to chemotherapy via activating WNT pathway through miR‐4701‐5p/NFE2L1 axis.