Citation

Graudenz MS, Uchoa DM, Cadore E, Giacomazzi J, Callegari-Jacques SM (2019) Αβ-Crystallin and Laminin-332 are Prognostic Markers for Triple Negative Breast Cancers in a Brazilian Series. Int J Cancer Clin Res 6:103. doi.org/10.23937/2378-3419/1410103

Copyright

© 2019 Graudenz MS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

RESEARCH ARTICLE | OPEN ACCESSDOI: 10.23937/2378-3419/1410103

Αβ-Crystallin and Laminin-332 are Prognostic Markers for Triple Negative Breast Cancers in a Brazilian Series

Marcia S Graudenz1,2*, Diego M Uchoa2, Ermani Cadore2, Juliana Giacomazzi3 and Sidia Maria Callegari-Jacques2,4

1Departmento de Patologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

2Programa de Pos Graduação Ciencias Médicas, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

3Instituto do Câncer, Hospital Tacchini, Bento Gonçalves, Brazil

4Departamento de Estatistica, Instituto de Matematica, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

Abstract

Purpose

Association between increased αβ-crystallin (ABC) and abnormal LN332 (LN332) expression in triple negative (TNBC) and basal-like (BLBC) breast cancers has been suggested recently. This study aims to evaluate ABC and LN332 immunohistochemical expression in a series of TN infiltrating ductal breast carcinomas and its association with clinical-pathological features and prognostic significance.

Methods

Microarrays of 69 cases of TNBC cases were scored for the expression of ABC, LN332, CK5/6 and EGFR by immunohistochemistry with linked clinical and pathological data (age, tumor size, lymph node metastases, histological grade and subtype, lymphovascular invasion). Tumors were scored as strong, moderate and weakly positive for these biomarkers.

Results

ABC was expressed in 72.7% (48/66) and LN332 in 63.8% (44/69) of cases. ABC immunostaining was predominantly cytoplasmic (73.5%) and LN332 was exclusively cytoplasmic (100%). ABC was expressed in 83% of BLBC, followed by the penta negative profile (17%). The 5-year survival was 0.67 and 0.75 for ABC negative and LN332 positive tumors, respectively. For the BLBC group this probability was 0.67, while in the penta negative group (ABC, LN332, CK5/6 and EGFR) it was only 0.37. ABC-/LN332+ profile was associated with longer probability of non-recurrence (10-years probability: 0.86 for ABC-/LN332+ tumors versus 0.36 for other profiles; P = 0.021) and longer cumulative survival (10-years probability: 1.0 for ABC-/LN332+ tumors versus 0.53 for other profiles; P = 0.031). There was no association between the ABC-negative/LN332-positive profile and BLBC.

Conclusions

ABC and LN332 are commonly expressed in TNBC, especially in BLBC. TNBC with ABC-/LN332+ profile showed better clinical outcome.