Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway
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Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway
Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway
中国结合医学杂志(英文版)2012年18卷第12期 页码:934-941
Affiliations:
1. Department of Hematology, Qilu Hospital of Shandong University,Jinan,China
2. Research Center, Xiyuan Hospital of China Academy of Chinese Medical Sciences,Beijing,China
3. Department of Scientific Research, Qilu Hospital of Shandong University,Jinan,China
4. Department of Health Care, Qilu Hospital of Shandong University,Jinan,China
Author bio:
Funds:
Supported by the National Natural Science Foundation of China (No. 81102710)
Wang, R., Cong, Wh., Guo, G. et al. Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway., Chin. J. Integr. Med. 18, 934–941 (2012). https://doi.org/10.1007/s11655-012-1297-z
Ran Wang, Wei-hong Cong, Gang Guo, et al. Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway[J]. Chinese Journal of Integrative Medicine, 2012,18(12):934-941.
Wang, R., Cong, Wh., Guo, G. et al. Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway., Chin. J. Integr. Med. 18, 934–941 (2012). https://doi.org/10.1007/s11655-012-1297-zDOI:
Ran Wang, Wei-hong Cong, Gang Guo, et al. Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway[J]. Chinese Journal of Integrative Medicine, 2012,18(12):934-941. DOI: 10.1007/s11655-012-1297-z.
Synergism between carnosic acid and arsenic trioxide on induction of acute myeloid leukemia cell apoptosis is associated with modulation of PTEN/Akt signaling pathway
摘要
To investigate the synergistic effects of carnosic acid (CA) with arsenic trioxide (As2O3) on proliferation and apoptosis in HL-60 human myeloid leukemia cells
and the major cellular signaling pathway involved in these effects. HL-60 cellular proliferation was measured by 3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide (MTT) analysis. Cell cycle distribution and apoptosis were monitored by flow cytometry. The activation of casepase-9
Bcl-2-associated agonist of cell death (BAD)
p-BAD
p27
phosphatase and tensin homolog deleted on chromosome ten (PTEN)
Akt
p-Akt was assessed by Western blot analysis. The expression of PTEN mRNA was tested by reverse transcription polymerase chain reaction (RT-PCR) analysis. CA reduced HL-60 cell viability in a dose- and time-dependent manner
and induced G1 arrest and apoptosis. Moreover
CA upregulated PTEN expression
blocked the Akt signaling pathway
subsequently inhibited phosphorylation of BAD
reactivated caspase-9
and elevated levels of p27. CA also augmented these effects of As2O3. CA might be a novel candidate of the combination therapy for leukemia treatment; these effects were apparently associated with the modulation of PTEN/Akt signaling pathway.
Abstract
To investigate the synergistic effects of carnosic acid (CA) with arsenic trioxide (As2O3) on proliferation and apoptosis in HL-60 human myeloid leukemia cells
and the major cellular signaling pathway involved in these effects. HL-60 cellular proliferation was measured by 3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide (MTT) analysis. Cell cycle distribution and apoptosis were monitored by flow cytometry. The activation of casepase-9
Bcl-2-associated agonist of cell death (BAD)
p-BAD
p27
phosphatase and tensin homolog deleted on chromosome ten (PTEN)
Akt
p-Akt was assessed by Western blot analysis. The expression of PTEN mRNA was tested by reverse transcription polymerase chain reaction (RT-PCR) analysis. CA reduced HL-60 cell viability in a dose- and time-dependent manner
and induced G1 arrest and apoptosis. Moreover
CA upregulated PTEN expression
blocked the Akt signaling pathway
subsequently inhibited phosphorylation of BAD
reactivated caspase-9
and elevated levels of p27. CA also augmented these effects of As2O3. CA might be a novel candidate of the combination therapy for leukemia treatment; these effects were apparently associated with the modulation of PTEN/Akt signaling pathway.
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