Specific requirement for Bax, not Bak, in Myc-induced apoptosis and tumor suppression in vivo

Tobias B. Dansen, Jonathan Whitfield, Fanya Rostker, Lamorna Brown-Swigart, Gerard I. Evan*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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 β 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.

Original languageEnglish
Pages (from-to)10890-10895
Number of pages6
JournalJournal of Biological Chemistry
Volume281
Issue number16
DOIs
Publication statusPublished - 21 Apr 2006
Externally publishedYes

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