Role of discoidin domain receptor 2 (DDR2) and microRNA-182 in survival of women with high-grade serous ovarian cancer.
Aged
Discoidin Domain Receptor 2
/ genetics
Disease Progression
Disease-Free Survival
Female
Humans
Immunohistochemistry
/ methods
MicroRNAs
/ genetics
Middle Aged
Neoplasm Staging
/ methods
Neoplasm, Residual
/ drug therapy
Organoplatinum Compounds
/ therapeutic use
Ovarian Neoplasms
/ drug therapy
Retrospective Studies
Epithelial ovarian cancer
biomarkers
drug resistance
prognosis
survival
Journal
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
ISSN: 1423-0380
Titre abrégé: Tumour Biol
Pays: Netherlands
ID NLM: 8409922
Informations de publication
Date de publication:
Jan 2019
Jan 2019
Historique:
entrez:
28
2
2019
pubmed:
28
2
2019
medline:
2
3
2019
Statut:
ppublish
Résumé
The objective of this study is to evaluate the relationship between discoidin domain receptor 2 (DDR2) and miR-182 expression with response to platinum-based chemotherapy and survival in women with high-grade serous ovarian cancer (HGSOC). We evaluated 78 women with HGSOC stages I-IV, diagnosed between 1996 and 2013, and followed up until 2016. DDR2 expression was assessed using immunohistochemistry on tissue microarray slides. The microRNAs were evaluated by qRT-PCR. DDR2 expression was high in 11 (14.1%) women. PFS was significantly lower in women with FIGO stage I/II - versus III/IV, post-surgery residual disease and high expression of DDR2. Women with postsurgery residual disease, FIGO stage I/II - versus III/IV and DDR2 expression had worse OS, but only post-surgery residual disease remained an independent prognostic factor for worse OS in multivariable analysis. miR-182 expression levels were significantly lower in patients harboring tumors with higher expression of DDR2 (p < 0.001). In this relatively large cohort of women with HSGOC, higher DDR2 expression was associated with lower miR-182 levels and worse PFS, suggesting that these molecules may be associated with mechanisms of HGSOC progression.
Identifiants
pubmed: 30810094
doi: 10.1177/1010428318823988
doi:
Substances chimiques
MicroRNAs
0
Mirn182 microRNA, human
0
Organoplatinum Compounds
0
DDR2 protein, human
EC 2.7.10.1
Discoidin Domain Receptor 2
EC 2.7.10.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM