The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Bim is a suppressor of Myc-induced mouse B cell leukemia
Open accessAbstract
Impaired apoptosis is now recognized to be central to tumor development. Bcl2, activated by chromosomal translocation in human follicular lymphoma, promotes oncogenesis by inhibiting apoptosis. Bim, a distant proapoptotic relative, is emerging as a major physiologic antagonist of Bcl2. Here, we show that loss of Bim is oncogenic. Bim protein levels were elevated in the apoptosis-prone B lymphoid cells of Eμ- Myc -transgenic mice, and Bim -mutant Eμ- Myc mice had increased numbers of IgM-bearing B cells. Eμ- Myc -expressing B lymphoid cells deficient in Bim were refractory to apoptosis induced in vitro by cytokine deprivation or antigen receptor cross-linking. Thus, Bim is induced by Myc in B cells and mediates apoptosis. Remarkably, inactivation of even a single allele of Bim accelerated Myc-induced development of tumors, particularly acute B cell leukemia. None of the primary tumors from Bim +/- Eμ- Myc mice displayed loss of the second allele of Bim . These findings indicate that Bim is a tumor suppressor, at least in B lymphocytes, and is haploinsufficient. Whereas the p19Arf/p53 pathway is frequently mutated in tumors arising in Bim + / + Eμ- Myc mice, it was unaffected in most Bim-deficient tumors, indicating that Bim reduction is an effective alternative to loss of p53 function.
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Cites
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Metadata
- Authors
- Egle, A., Harris, A. W., Bouillet, P., & Cory, S.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2004-04-12
- Volume
- 101
- Issue
- 16
- Pages
- 6164-6169
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2013194319
- Cited by
- 488
- References
- 7
- FWCI
- 10.50
- Type
- journal article
- Language
- en
- Open access
- bronze
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