Cargando…

Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer

Nectins are Ca(2+)-independent immunoglobulin-like cell adhesion molecules that compose a family of four members that regulate several cellular activities such as movement, proliferation, survival, differentiation, polarization, and the entry of viruses. Nectin-4 has recently emerged as a metastatis...

Descripción completa

Detalles Bibliográficos
Autores principales: Lattanzio, R, Ghasemi, R, Brancati, F, Sorda, R L, Tinari, N, Perracchio, L, Iacobelli, S, Mottolese, M, Natali, P G, Piantelli, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183981/
https://www.ncbi.nlm.nih.gov/pubmed/25178039
http://dx.doi.org/10.1038/oncsis.2014.32
_version_ 1782337774380122112
author Lattanzio, R
Ghasemi, R
Brancati, F
Sorda, R L
Tinari, N
Perracchio, L
Iacobelli, S
Mottolese, M
Natali, P G
Piantelli, M
author_facet Lattanzio, R
Ghasemi, R
Brancati, F
Sorda, R L
Tinari, N
Perracchio, L
Iacobelli, S
Mottolese, M
Natali, P G
Piantelli, M
author_sort Lattanzio, R
collection PubMed
description Nectins are Ca(2+)-independent immunoglobulin-like cell adhesion molecules that compose a family of four members that regulate several cellular activities such as movement, proliferation, survival, differentiation, polarization, and the entry of viruses. Nectin-4 has recently emerged as a metastatis-associated protein in several cancers. Here, we have evaluated the association between the expression of Nectin-4 and the clinical outcome of patients with node-negative, T1/T2 breast cancers.The study group consisted of 197 patients presenting with primary unilateral breast carcinoma (T1/T2), with no evidence of nodal involvement and distant metastases. Nectin-4 protein expression was assessed by immunohistochemistry on tissue microarrays, and the results correlated with the clinical data using Kaplan–Meier curves and multivariate Cox regression analysis. Thirty-four out of 197 tumors (17.3%) exhibited Nectin-4 expression on cell membrane (m-Nectin-4) and 122 out of the 163m-Nectin-4 negative tumors (74.8%) showed high cytoplasmic expression of Nectin-4 (c-Nectin-4(High)). At Kaplan–Meier analysis, m-Nectin-4 positivity was significantly associated with a lower disease-free survival (DFS) and distant relapse-free survival (DRFS) rate in patients with a luminal-A phenotype (P=0.030 and P=0.002, respectively). Multivariate analysis showed that in luminal-A tumors m-Nectin-4 positivity is an independent prognostic factor for DFS (P=0.018) and DRFS (P=0.004), but not for local relapse-free survival (LRFS). On the other hand, c-Nectin-4(High) was significantly associated with higher rates of DFS and LRFS, but not DRFS, in the whole population (P=0.008 and P=0.004, respectively) and in patients with luminal-A tumors (P=0.022 and P=0.018, respectively). In patients with luminal-A tumors, multivariate analysis showed that the prognostic value of c-Nectin-4(Low/Negative) is limited to DFS (P=0.012) and LRFS (P=0.022). We suggest that Nectin-4 represents a prognostic factor and a therapeutic target in luminal-A early stage breast cancer.
format Online
Article
Text
id pubmed-4183981
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-41839812014-10-03 Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer Lattanzio, R Ghasemi, R Brancati, F Sorda, R L Tinari, N Perracchio, L Iacobelli, S Mottolese, M Natali, P G Piantelli, M Oncogenesis Original Article Nectins are Ca(2+)-independent immunoglobulin-like cell adhesion molecules that compose a family of four members that regulate several cellular activities such as movement, proliferation, survival, differentiation, polarization, and the entry of viruses. Nectin-4 has recently emerged as a metastatis-associated protein in several cancers. Here, we have evaluated the association between the expression of Nectin-4 and the clinical outcome of patients with node-negative, T1/T2 breast cancers.The study group consisted of 197 patients presenting with primary unilateral breast carcinoma (T1/T2), with no evidence of nodal involvement and distant metastases. Nectin-4 protein expression was assessed by immunohistochemistry on tissue microarrays, and the results correlated with the clinical data using Kaplan–Meier curves and multivariate Cox regression analysis. Thirty-four out of 197 tumors (17.3%) exhibited Nectin-4 expression on cell membrane (m-Nectin-4) and 122 out of the 163m-Nectin-4 negative tumors (74.8%) showed high cytoplasmic expression of Nectin-4 (c-Nectin-4(High)). At Kaplan–Meier analysis, m-Nectin-4 positivity was significantly associated with a lower disease-free survival (DFS) and distant relapse-free survival (DRFS) rate in patients with a luminal-A phenotype (P=0.030 and P=0.002, respectively). Multivariate analysis showed that in luminal-A tumors m-Nectin-4 positivity is an independent prognostic factor for DFS (P=0.018) and DRFS (P=0.004), but not for local relapse-free survival (LRFS). On the other hand, c-Nectin-4(High) was significantly associated with higher rates of DFS and LRFS, but not DRFS, in the whole population (P=0.008 and P=0.004, respectively) and in patients with luminal-A tumors (P=0.022 and P=0.018, respectively). In patients with luminal-A tumors, multivariate analysis showed that the prognostic value of c-Nectin-4(Low/Negative) is limited to DFS (P=0.012) and LRFS (P=0.022). We suggest that Nectin-4 represents a prognostic factor and a therapeutic target in luminal-A early stage breast cancer. Nature Publishing Group 2014-09 2014-09-01 /pmc/articles/PMC4183981/ /pubmed/25178039 http://dx.doi.org/10.1038/oncsis.2014.32 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Lattanzio, R
Ghasemi, R
Brancati, F
Sorda, R L
Tinari, N
Perracchio, L
Iacobelli, S
Mottolese, M
Natali, P G
Piantelli, M
Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer
title Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer
title_full Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer
title_fullStr Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer
title_full_unstemmed Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer
title_short Membranous Nectin-4 expression is a risk factor for distant relapse of T1-T2, N0 luminal-A early breast cancer
title_sort membranous nectin-4 expression is a risk factor for distant relapse of t1-t2, n0 luminal-a early breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183981/
https://www.ncbi.nlm.nih.gov/pubmed/25178039
http://dx.doi.org/10.1038/oncsis.2014.32
work_keys_str_mv AT lattanzior membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT ghasemir membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT brancatif membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT sordarl membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT tinarin membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT perracchiol membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT iacobellis membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT mottolesem membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT natalipg membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer
AT piantellim membranousnectin4expressionisariskfactorfordistantrelapseoft1t2n0luminalaearlybreastcancer