Upregulated osteoprotegerin expression promotes lung cancer cell invasion by increasing miR-20a expression

xlomafota13 shared this article with you from Inoreader Upregulated osteoprotegerin expression promotes lung cancer cell invasion by increasing miR-20a expression Via Experimental and therapeutic medicine Exp Ther Med. 2021 Aug;22(2):846. doi: 10.3892/etm.2021.10278. Epub 2021 Jun 7. ABSTRACT Osteoprotegerin (OPG) is a member of the tumor necrosis factor receptor superfamily and a major regulatory factor in osteoclast development. OPG has been previously associated with the malignant behavior of various types of cancer, particularly that of cancer metastasis. However, information on the link between the expression profile of OPG and lung cancer metastasis remained elusive. In the present study, the expression levels of OPG in the serum samples of patients with non-small cell lung cancer (NSCLC) was measured using ELISA. The expression of miRNAs was assessed using reverse transcription-quantitative PCR. A549 or H3122 cell invasion was assessed using Transwell invasion assays. The effect of OPG on the invasiveness of lung cancer cells was evaluated using an experimental mouse lung metastasis model. OPG expression was found to be upregulat ed in the serum of patients with NSCLC compared with that in healthy individuals. The serum levels of OPG in patients with distant metastasis were observably higher compared with those in patients without metastasis. Functionally, overexpression of OPG in NSCLC cells markedly promoted cell invasion. Mechanistically, increased expression of OPG resulted in upregulation of microRNA (miR)-20a in NSCLC cells. Furthermore, miR-20a promoted NSCLC cell invasion, whilst miR-20a inhibition partially abrogated the effect of OPG on NSCLC cell invasion. Taken together, the present results demonstrated that the OPG/miR-20a axis serve an important role in lung cancer metastasis, which potentially provide an additional novel target for lung cancer treatment. PMID:34149892 | PMC:PMC8210324 | DOI:10.3892/etm.2021.10278 View on the web Inoreader. Take back control of your news feed. Follow us on Twitter and Facebook.