Bad-deficient mice develop diffuse large B cell lymphoma.

Abstract:

:The proapoptotic activity of the "BH3-only" molecule BAD can be differentially regulated by survival factor signaling. Bad-deficient mice lacking both BAD long and BAD short proteins proved viable, and most cell types appeared to develop normally. BAD did not exclusively account for cell death after withdrawal of survival factors, but it was an intermediate for epidermal growth factor- or insulin-like growth factor I-countered apoptosis, consistent with a "sensitizing" BH3-only molecule. Lymphocytes developed normally with no premalignant hyperplasia, but they displayed subtle abnormalities in proliferation and IgG production. Despite the minimal phenotype, Bad-deficient mice progressed, with aging, to diffuse large B cell lymphoma of germinal center origin. Exposure of Bad-null mice to sublethal gamma-irradiation resulted in an increased incidence of pre-T cell and pro-/pre-B cell lymphoblastic leukemia/lymphoma. Thus, proapoptotic BAD suppresses tumorigenesis in the lymphocyte lineage.

authors

Ranger AM,Zha J,Harada H,Datta SR,Danial NN,Gilmore AP,Kutok JL,Le Beau MM,Greenberg ME,Korsmeyer SJ

doi

10.1073/pnas.1533446100

keywords:

subject

Has Abstract

pub_date

2003-08-05 00:00:00

pages

9324-9

issue

16

eissn

0027-8424

issn

1091-6490

pii

1533446100

journal_volume

100

pub_type

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