EP3 Is an Independent Prognostic Marker Only for Unifocal Breast Cancer Cases.
breast cancer
focality
multifocal
prognosis
prostaglandin E2 receptor 3 (EP3)
unifocal
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
22 Jun 2020
22 Jun 2020
Historique:
received:
27
05
2020
revised:
16
06
2020
accepted:
18
06
2020
entrez:
26
6
2020
pubmed:
26
6
2020
medline:
20
3
2021
Statut:
epublish
Résumé
The aim of this study was to evaluate the prognostic impact of prostaglandin E2 receptor 3 (EP3) receptor expression might have on the two different breast cancer entities: multifocal/multicentric versus unifocal. As the prognosis determining aspects, we investigated the overall- and disease-free survival by uni-and multivariate analysis. To underline the study's conclusion, we additionally considered the histopathological grading and the tumor node metastasis (TNM) staging system. A retrospective statistical analysis was performed on survival related events in a series of 289 sporadic breast cancer (BC) patients treated at the Department of Obstetrics and Gynecology at the Ludwig-Maximillian's University in Munich between 2000 and 2002. The EP3 receptor expression was analyzed by immunohistochemistry and showed to have a significantly positive association with breast cancer prognosis for both entities, although with major differences. Patients with unifocal BC with EP3 receptor expression showed a significant improved overall survival, in contrast to the patient cohort with multifocal/multicentric BC. In this group, EP3 expression revealed its positive impact merely five years after initial diagnosis. Underlining the positive influence of EP3 as a positive prognosticator notably for unifocal breast cancer, only this patient cohort showed favorable outcomes in staging and grading. Especially EP3 expression in unifocal breast cancer was identified as an independent prognostic marker for the overall survival, when adjusted for age, grading, and staging. Altogether, our results strengthen the need to further investigate the behavior of EP3 in breast cancer and understand why markers linked to inflammation show different effects on prognosis and clinicopathological parameters on each focality type.
Identifiants
pubmed: 32580276
pii: ijms21124418
doi: 10.3390/ijms21124418
pmc: PMC7352354
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
PTGER3 protein, human
0
Receptors, Estrogen
0
Receptors, Progesterone
0
Receptors, Prostaglandin E, EP3 Subtype
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
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