p53 and BLC2 Immunohistochemical Expression Across Molecular Subtypes in 1099 Early Breast Cancer Patients With Long-Term Follow-up: An Observational Study.
Adult
Aged
Aged, 80 and over
Antineoplastic Agents, Hormonal
/ therapeutic use
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Biomarkers, Tumor
/ analysis
Breast
/ pathology
Breast Neoplasms
/ diagnosis
Chemotherapy, Adjuvant
/ methods
Disease-Free Survival
Female
Follow-Up Studies
Humans
Immunohistochemistry
Kaplan-Meier Estimate
Mastectomy
Middle Aged
Neoplasm Recurrence, Local
/ epidemiology
Prognosis
Proto-Oncogene Proteins c-bcl-2
/ analysis
Receptors, Progesterone
Tumor Suppressor Protein p53
/ analysis
Young Adult
Immunohistochemistry
Individualized medicine
Prognosis
Prognostic factors
TP53
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
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-e770Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.