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miR-519d-3p suppresses tumorigenicity and metastasis by inhibiting Bcl-w and HIF-1α in NSCLCopen access

Authors
Choi, Jae YeonSeok, Hyun JeongKim, Rae-KwonChoi, Mi YoungLee, Su-JaeBae, 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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