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High TNFRSF12A level associated with MMP-9 overexpression is linked to poor prognosis in breast cancer: Gene set enrichment analysis and validation in large-scale cohortsopen access

Authors
Yang, JunghoMin, Kyueng-WhanKim, Dong-HoonSon, Byoung KwanMoon, Kyoung MinWi, Young ChanBang, Seong SikOh, Young HaDo, Sung-ImChae, Seoung WanOh, SukjoongKim, Young HwanKwon, Mi Jung
Issue Date
Aug-2018
Publisher
PUBLIC LIBRARY SCIENCE
Citation
PLOS ONE, v.13, no.8, pp.1 - 13
Indexed
SCIE
SCOPUS
Journal Title
PLOS ONE
Volume
13
Number
8
Start Page
1
End Page
13
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/149642
DOI
10.1371/journal.pone.0202113
ISSN
1932-6203
Abstract
Background Matrix metalloproteinase-9 (MMP-9) is associated with remodelling of the extracellular matrix and invasion in various cancers. Identifying proteins connected to high MMP-9 expression is important in explaining its mechanisms. Our study aims to shed light on genes associated with high MMP-9 expression and to discuss their clinical impact in breast cancer. Methods We evaluated 173 breast cancer cases from the Kangbuk Samsung Hospital, with 1964 cases from the Molecular Taxonomy of Breast Cancer International Consortium database serving as a validation cohort. We investigated relationships between MMP-9 expression and clinicopathological characteristics. We then used gene set enrichment analyses to detect the association of genes with MMP-9 overexpression, and performed survival analyses to determine the significance of the gene in three independent cohorts. Results High MMP-9 expression correlated with poor prognosis in univariate and multivariate analyses. Using gene set enrichment analysis, we found that tumour necrosis factor receptor superfamily member 12A (TNFRSF12A) was linked to high MMP-9 expression. In the survival analysis of three published data sets (METABRIC, GSE1456, GSE20685), high TNFRSF12A was relevant to a poor survival rate. Conclusions High levels of TNFRSF12A associated with MMP-9 overexpression may be important to explain the progression of breast cancer, and survival could be improved using therapy targeting TNFRSF12A.
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