Curcumin-induced apoptosis in human leukemia cell HL-60 is associated with inhibition of telomerase activity

S Mukherjee, U Ghosh, NP Bhattacharyya… - Molecular and Cellular …, 2007 - Springer
S Mukherjee, U Ghosh, NP Bhattacharyya, RK Bhattacharya, S Dey, M Roy
Molecular and Cellular Biochemistry, 2007Springer
Curcumin (diferuloylmethane), a natural cancer chemopreventive compound, has been
tested for its action in acute myeloblastic leukemia cell line HL-60. The results clearly show
that curcumin induces apoptosis in these cells as evidenced by the release of cytochrome c
from mitochondria to the cytosol and increase in the DNA content in sub G1 region as
observed in FACS analysis. Apoptosis is apparently mediated by up-regulation of apoptotic
gene bax and simultaneous down-regulation of anti-apoptotic gene bcl-2 followed by …
Abstract
Curcumin (diferuloylmethane), a natural cancer chemopreventive compound, has been tested for its action in acute myeloblastic leukemia cell line HL-60. The results clearly show that curcumin induces apoptosis in these cells as evidenced by the release of cytochrome c from mitochondria to the cytosol and increase in the DNA content in sub G1 region as observed in FACS analysis. Apoptosis is apparently mediated by up-regulation of apoptotic gene bax and simultaneous down-regulation of anti-apoptotic gene bcl-2 followed by activation of caspases 3 and 8 and degradation of PARP. Telomerase, a reverse transcriptase, has been found to be activated in more than 80% of human cancers and, therefore, can be considered as a potential marker for tumorigenesis. Certain natural compounds have the potential of inhibiting telomerase activity leading to suppression of cell viability and induction of apoptosis. The present study shows that curcumin-induced apoptosis coincides with the inhibition of telomerase activity in a dose dependent manner.
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