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Specific requirement for Bax, not Bak, in Myc-induced apoptosis and tumor suppression in vivo.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2006 Apr 21; Vol. 281 (16), pp. 10890-5. Date of Electronic Publication: 2006 Feb 07. - Publication Year :
- 2006
-
Abstract
- Bax and Bak comprise the mitochondrial gateway for apoptosis induced by diverse stimuli. Loss of both bax and bak is necessary to block cell death induced by such stimuli, indicating a great degree of functional overlap between Bax and Bak. Apoptosis is the major intrinsic pathway that limits the oncogenic potential of Myc. Using a switchable mouse model of Myc-induced apoptosis in pancreatic beta cells, we have shown that Myc induces apoptosis in vivo exclusively through Bax but not Bak. Furthermore, blockade of Myc-induced apoptosis by the inactivation of Bax, but not Bak, eliminates all restraints to the oncogenic potential of Myc, allowing the rapid and synchronous progression of invasive, angiogenic tumors.
- Subjects :
- Animals
Antineoplastic Agents, Hormonal pharmacology
Cell Proliferation
Glucagon metabolism
Immunohistochemistry
In Situ Nick-End Labeling
Insulin-Secreting Cells metabolism
Mice
Mice, Transgenic
Microscopy, Confocal
Microscopy, Fluorescence
Neoplasm Invasiveness
Neoplasms, Experimental metabolism
Neovascularization, Pathologic
Pancreas metabolism
Tamoxifen pharmacology
Apoptosis
Gene Expression Regulation, Neoplastic
Neoplasms metabolism
Neoplasms, Experimental pathology
Proto-Oncogene Proteins c-myc metabolism
bcl-2 Homologous Antagonist-Killer Protein metabolism
bcl-2-Associated X Protein metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 281
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 16464852
- Full Text :
- https://doi.org/10.1074/jbc.M513655200