Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0134496
Title: The A allele at rs13419896 of EPAS1 is associated with enhanced expression and poor prognosis for non-small cell lung cancer
Authors: Putra A.C.
Eguchi H.
Lee K.L. 
Yamane Y.
Gustine E.
Isobe T.
Nishiyama M.
Hiyama K.
Poellinger L. 
Tanimoto K.
Issue Date: 2015
Publisher: Public Library of Science
Citation: Putra A.C., Eguchi H., Lee K.L., Yamane Y., Gustine E., Isobe T., Nishiyama M., Hiyama K., Poellinger L., Tanimoto K. (2015). The A allele at rs13419896 of EPAS1 is associated with enhanced expression and poor prognosis for non-small cell lung cancer. PLoS ONE 10 (8) : e0134496. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0134496
Abstract: Hypoxia-inducible factor-2α (HIF-2α, or EPAS1) is important for cancer progression, and is a putative biomarker for poor prognosis for non-small cell lung cancer (NSCLC). However, molecular mechanisms underlying the EPAS1 overexpression are not still fully understood. We explored a role of a single nucleotide polymorphism (SNP), rs13419896 located within intron 1 of the EPAS1 gene in regulation of its expression. Bioinformatic analyses suggested that a region including the rs13419896 SNP plays a role in regulation of the EPAS1 gene expression and the SNP alters the binding activity of transcription factors. In vitro analyses demonstrated that a fragment containing the SNP locus function as a regulatory region and that a fragment with A allele showed higher transactivation activity than one with G, especially in the presence of overexpressed c-Fos or c-Jun. Moreover, NSCLC patients with the A allele showed poorer prognosis than those with G at the SNP even after adjustment with various variables. In conclusion, the genetic polymorphism of the EPAS1 gene may lead to variation of its gene expression levels to drive progression of the cancer and serve as a prognostic marker for NSCLC. © 2015 Putra et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/164152
ISSN: 19326203
DOI: 10.1371/journal.pone.0134496
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