miR-519d-3p suppresses tumorigenicity and metastasis by inhibiting Bcl-w and HIF-1α in NSCLCopen access
- Authors
- Choi, Jae Yeon; Seok, Hyun Jeong; Kim, Rae-Kwon; Choi, Mi Young; Lee, Su-Jae; Bae, In Hwa
- Issue Date
- Sep-2021
- Publisher
- Nature Publishing Group
- Keywords
- Bcl-w; HIF-1α; hypoxia; miR-519d-3p; NSCLC; solid tumor
- Citation
- Molecular Therapy - Oncolytics, v.22, pp 368 - 379
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Molecular Therapy - Oncolytics
- Volume
- 22
- Start Page
- 368
- End Page
- 379
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/194069
- DOI
- 10.1016/j.omto.2021.06.015
- ISSN
- 2372-7705
2372-7705
- Abstract
- Bcl-w, a member of the Bcl-2 family, is highly expressed in various solid tumor, including lung cancer, suggesting that it is involved in cancer cell survival and carcinogenesis. Solid cancer-induced hypoxia has been reported to increase angiogenesis, growth factor, gene instability, invasion, and metastasis. Despite many studies on the treatment of non-small cell lung cancer (NSCLC) with a high incidence rate, the survival rate of patients has not improved because the cancer cells acquired resistance to treatment. This study investigated the correlation between Bcl-w expression and hypoxia in tumor malignancy of NSCLC. Meanwhile, microRNAs (miRNAs) are involved in a variety of key signaling mechanisms associated with hypoxia. Therefore, we discovered miR-519d-3p, which inhibits the expression of Bcl-w and hypoxia-inducing factor (HIF)-1α, and found that it reduces hypoxia-induced tumorigenesis. Spearman's correlation analysis showed that the expression levels of miR-519d-3p and Bcl-w/HIF-1α were negatively correlated, respectively. This showed that miR-519d-3p can be used as a diagnostic biomarker and target therapy for NSCLC.
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