TY - JOUR
T1 - Glucocorticoids, oxysterols, and cAMP with glucocorticoids each cause apoptosis of CEM cells and suppress c-myc
AU - Thompson, E. Brad
AU - Medh, Rheem D.
AU - Zhou, Feng
AU - Ayala-Torres, Sylvette
AU - Ansari, Naseem
AU - Zhang, Weiping
AU - Johnson, Betty H.
N1 - Funding Information:
The authors wish to thank G. Marcano for technical assistance and M. ElNaghy for the cloning of M10R5 cells. This work was supported in part by 2RO1CA1407 grant from the National Institutes of Health, National Cancer Institute and The Wall Medical Research Foundation.
PY - 1999/4
Y1 - 1999/4
N2 - In clones of the CEM human acute lymphoblastic leukemic cell line, glucocorticoids, oxysterols and activators of the cAMP pathway acting synergistically with glucocorticoids, each can cause apoptotic cell death. Morphologically and kinetically, these deaths resemble one another. The kinetics are striking: in each case, after addition of the lethal compound(s), an interval of approximately 24 h follows, during which cell growth continues unabated. During this 'prodromal' period, removal of the apoptotic agent leaves the cells fully viable. We hypothesize that a sequence of biochemical events occurs during the prodrome which eventually results in the triggering of the full apoptotic response as evidenced by the activation of caspases and DNA fragmentation. At some point, the process is irreversible and proceeds relatively rapidly to cell death. Suppression of c-Myc seems a universal early event evoked by each of these lethal compounds or combinations, and we conclude that the negative regulation of this proto- oncogene is an important aspect of the critical pre-apoptotic events in these cells.
AB - In clones of the CEM human acute lymphoblastic leukemic cell line, glucocorticoids, oxysterols and activators of the cAMP pathway acting synergistically with glucocorticoids, each can cause apoptotic cell death. Morphologically and kinetically, these deaths resemble one another. The kinetics are striking: in each case, after addition of the lethal compound(s), an interval of approximately 24 h follows, during which cell growth continues unabated. During this 'prodromal' period, removal of the apoptotic agent leaves the cells fully viable. We hypothesize that a sequence of biochemical events occurs during the prodrome which eventually results in the triggering of the full apoptotic response as evidenced by the activation of caspases and DNA fragmentation. At some point, the process is irreversible and proceeds relatively rapidly to cell death. Suppression of c-Myc seems a universal early event evoked by each of these lethal compounds or combinations, and we conclude that the negative regulation of this proto- oncogene is an important aspect of the critical pre-apoptotic events in these cells.
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U2 - 10.1016/S0960-0760(99)00063-1
DO - 10.1016/S0960-0760(99)00063-1
M3 - Article
C2 - 10419025
AN - SCOPUS:0033015171
SN - 0960-0760
VL - 69
SP - 453
EP - 461
JO - Journal of Steroid Biochemistry and Molecular Biology
JF - Journal of Steroid Biochemistry and Molecular Biology
IS - 1-6
ER -