p53 and BLC2 Immunohistochemical Expression Across Molecular Subtypes in 1099 Early Breast Cancer Patients With Long-Term Follow-up: An Observational Study.


Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
12 2020
Historique:
received: 23 01 2020
revised: 03 04 2020
accepted: 06 05 2020
pubmed: 26 6 2020
medline: 12 10 2021
entrez: 26 6 2020
Statut: ppublish

Résumé

p53 and antiapoptotic B-cell leukemia/lymphoma 2 (BLC2) have been proposed as prognostic markers for early breast cancer (BC), although their relationship with conventional parameters and patient prognosis, as well as their distribution within the molecular BC subtypes remains uncertain. In this observational study, we analyzed the immunohistochemical expression of p53 and BLC2 in 1099 early BC patients surgically treated between 2000 and 2006 and followed for at least 5 years, also considering their association with pathologic factors and molecular subtypes, as well as their influence on disease-free survival. p53 and BLC2 are distributed differently across molecular subtypes (P < .0001); in particular, p53 positivity and BLC2 negativity seems to be associated with more aggressive conventional tumor phenotypes. Moreover, BLC2 negativity seems to be a significant discriminating factor for disease-free survival (P = .003) according to Kaplan-Meier analysis, while p53 seems to have no discriminating effect. Among patients with discordant p53/BLC2 phenotype, the combination p53 These two biomarkers, in addition to conventional pathologic factors and molecular subtype, could help define the risk and outcome of BC.

Identifiants

pubmed: 32580907
pii: S1526-8209(20)30107-5
doi: 10.1016/j.clbc.2020.05.005
pii:
doi:

Substances chimiques

Antineoplastic Agents, Hormonal 0
BCL2 protein, human 0
Biomarkers, Tumor 0
Proto-Oncogene Proteins c-bcl-2 0
Receptors, Progesterone 0
TP53 protein, human 0
Tumor Suppressor Protein p53 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e761-e770

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Alessandra Fabi (A)

Division of Medical Oncology 1, IRCCS, Regina Elena National Cancer Institute, Rome, Italy. Electronic address: alessandra.fabi@ifo.gov.it.

Marcella Mottolese (M)

Division of Pathology, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Anna Di Benedetto (A)

Division of Pathology, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Francesca Sperati (F)

San Gallicano Dermatological Institute, IRCCS, Rome, Italy.

Cristiana Ercolani (C)

Division of Pathology, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Simonetta Buglioni (S)

Division of Pathology, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Cecilia Nisticò (C)

Division of Medical Oncology 1, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Gianluigi Ferretti (G)

Division of Medical Oncology 1, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Patrizia Vici (P)

Division of Medical Oncology 2, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Letizia Perracchio (L)

Division of Pathology, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Paola Malaguti (P)

Division of Medical Oncology 1, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Michelangelo Russillo (M)

Division of Medical Oncology 1, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Claudio Botti (C)

Department of Surgery, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Edoardo Pescarmona (E)

Division of Pathology, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

Francesco Cognetti (F)

Division of Medical Oncology 1, IRCCS, Regina Elena National Cancer Institute, Rome, Italy; Department of Medical Oncology, Università di Roma "La Sapienza", Rome, Italy.

Irene Terrenato (I)

Biostatistics and Bioinformatic Unit, Scientific Direction, IRCCS, Regina Elena National Cancer Institute, Rome, Italy.

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Classifications MeSH