TY - JOUR
T1 - Specific requirement for Bax, not Bak, in Myc-induced apoptosis and tumor suppression in vivo
AU - Dansen, Tobias B.
AU - Whitfield, Jonathan
AU - Rostker, Fanya
AU - Brown-Swigart, Lamorna
AU - Evan, Gerard I.
PY - 2006/4/21
Y1 - 2006/4/21
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=33646348235&partnerID=8YFLogxK
U2 - 10.1074/jbc.M513655200
DO - 10.1074/jbc.M513655200
M3 - Article
C2 - 16464852
AN - SCOPUS:33646348235
SN - 0021-9258
VL - 281
SP - 10890
EP - 10895
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 16
ER -