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Expression of Bcl-2 Family Member Bid in Normal and Malignant Tissues

Authors :
Maryla Krajewska
Juan M. Zapata
Ivo Meinhold-Heerlein
Hirad Hedayat
Anne Monks
Herta Bettendorf
Ahmed Shabaik
Lukas Bubendorf
Olli-P. Kallioniemi
Hoguen Kim
Guido Reifenberger
John C. Reed
Stanislaw Krajewski
Source :
Neoplasia: An International Journal for Oncology Research, Vol 4, Iss 2, Pp 129-140 (2002)
Publication Year :
2002
Publisher :
Elsevier, 2002.

Abstract

Bid is the only known Bcl-2 family member that can function as an agonist of proapoptotic Bcl-2-related proteins such as Bax and Bak. Expression of the proapoptotic Bcl-2 family protein Bid was assessed by immunoblotting and immunohistochemical methods in normal murine and human tissues, and in several types of human cancers and tumor cell lines. Bid expression in normal tissues varied widely, with prominent Bid immunostaining occurring in several types of short-lived cells (e.g., germinal center B cells, peripheral blood granulocytes, differentiated keratinocytes) and in apoptosissensitive cells (e.g., adult neurons). Analysis of Bid expression by immunostaining of 100 colon, 95 ovarian, and 254 prostate cancers, as well as 59 brain tumors and 50 lymphomas, revealed evidence of altered Bid regulation in sometypes of cancers. Correlations with clinical outcome data revealed association of higher levels of Bid with longer recurrence-free survival in men with locally advanced (T3 stage) prostate cancer (P=0.04). Immunoblot analysis of Bid protein levels in the NCI's panel of 60 human tumor cell lines revealed a correlation between higher levels of Bid and sensitivity to ribonucleotide reductase (RR)-inhibiting drugs (P

Details

Language :
English
ISSN :
14765586 and 15228002
Volume :
4
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Neoplasia: An International Journal for Oncology Research
Publication Type :
Academic Journal
Accession number :
edsdoj.7937338c9d354259a347e2221fa7ac1a
Document Type :
article
Full Text :
https://doi.org/10.1038/sj.neo.7900222