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Nectin-4 Expression Is an Independent Prognostic Biomarker and Associated With Better Survival in Triple-Negative Breast Cancer.

Authors :
Zeindler J
Soysal SD
Piscuoglio S
Ng CKY
Mechera R
Isaak A
Weber WP
Muenst S
Kurzeder C
Source :
Frontiers in medicine [Front Med (Lausanne)] 2019 Sep 13; Vol. 6, pp. 200. Date of Electronic Publication: 2019 Sep 13 (Print Publication: 2019).
Publication Year :
2019

Abstract

Background: Triple-negative breast cancer (TNBC) represents about 10-20% of all invasive breast cancers and is associated with a poor prognosis. The nectin cell adhesion protein 4 (Nectin-4) is a junction protein involved in the formation and maintenance of cell junctions. Nectin-4 has previously shown to be expressed in about 60% of TNBC as well as in TNBC metastases, but to be absent in normal breast tissue, which makes it a potential specific target for TNBC therapy. Previous studies have shown an association of Nectin-4 protein expression with worse prognosis in TNBC in a small patient cohort. The aim of our study was to explore the role of Nectin-4 in TNBC and confirm its impact on survival in a larger TNBC patient cohort. Material and Methods: We performed immunohistochemical staining for Nectin-4 on a tissue microarray encompassing 148 TNBC cases with detailed clinical annotation and outcomes data. Results: A high expression of Nectin-4 was present in 86 (58%) of the 148 TNBC cases. In multivariate survival analysis, high expression of Nectin-4 was associated with a significantly better overall survival when compared with low expression of Nectin-4 ( p < 0.001). Nectin-4-high expression was also significantly associated with a lower tumor stage ( p = 0.025) and pN0 lymph node stage ( p = 0.034). Conclusion: Our results confirm that expression of Nectin-4 serves as a potential prognostic marker in TNBC and is associated with a significantly better overall survival. In addition, Nectin-4 represents a potential target in TNBC, and its role in molecular defined breast cancer subtype should be investigated in larger patient cohorts.<br /> (Copyright © 2019 Zeindler, Soysal, Piscuoglio, Ng, Mechera, Isaak, Weber, Muenst and Kurzeder.)

Details

Language :
English
ISSN :
2296-858X
Volume :
6
Database :
MEDLINE
Journal :
Frontiers in medicine
Publication Type :
Academic Journal
Accession number :
31572728
Full Text :
https://doi.org/10.3389/fmed.2019.00200