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Reduced expression of both Bax and Bcl‐2 is independently associated with lymph node metastasis in human breast carcinomas
Author(s) -
Bukholm Ida R. K.,
Bukholm Geir,
Nesland Jahn M.
Publication year - 2002
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1034/j.1600-0463.2002.100303.x
Subject(s) - univariate , immunohistochemistry , univariate analysis , oncology , lymph node , proportional hazards model , apoptosis , breast cancer , cancer research , multivariate analysis , pathology , medicine , biology , cancer , multivariate statistics , biochemistry , statistics , mathematics
Imbalance between pro‐apoptotic and anti‐apoptotic proteins, causing altered apoptosis, may lead to tumour development and tumour progression, and reduced response to adjuvant therapy. In this study, we evaluated the expression patterns of Bcl‐2, Bcl‐xL, and Bax protein in 126 primary invasive breast carcinomas, and the association with other clinicopathological parameters. We used immunohistochemical methods to evaluate protein expression. Reduced expression of both Bax and Bcl‐2 was associated with lymphnode metastases in univariate analyses (one‐way ANOVA) as well as in multivariate analysis (binary logistic regression) (Bcl‐2 p=0.003 univariate, p=0.01 multivariate, Bax p=0.05 univariate, p=0.03 multivariate). Bcl‐2 overexpression showed an inverse association with cyclin A (p=0.05), while expression of Bcl‐xL showed an association only with cyclin D3 (p=0.04). Bcl‐xL expression also showed a highly significant association with oestrogen receptor status (p=0.009). Bcl‐2 and Bcl‐xL showed an association with different D‐type cyclins, indicating different pathways of pathogenesis. Expression of Bcl‐2 was associated with better patient survival in univariate analysis (Kaplan meyer p=0.04), but lost its prognostic value in multivariate analysis (Cox regression p=0.2).