Xiao-ying, Z., Xiao-hong, Z., Lei, X. et al. Study on Taxol in inhibiting human leukemia cell proliferation and inducing apoptosis., Chin. J. Integr. Med. 10, 218–220 (2004). https://doi.org/10.1007/BF02836412
Zhao Xiao-ying, Zhang Xiao-hong, Xu Lei, et al. Study on Taxol in inhibiting human leukemia cell proliferation and inducing apoptosis[J]. Chinese Journal of Integrative Medicine, 2004,10(3):218-220.
Xiao-ying, Z., Xiao-hong, Z., Lei, X. et al. Study on Taxol in inhibiting human leukemia cell proliferation and inducing apoptosis., Chin. J. Integr. Med. 10, 218–220 (2004). https://doi.org/10.1007/BF02836412DOI:
Zhao Xiao-ying, Zhang Xiao-hong, Xu Lei, et al. Study on Taxol in inhibiting human leukemia cell proliferation and inducing apoptosis[J]. Chinese Journal of Integrative Medicine, 2004,10(3):218-220. DOI: 10.1007/BF02836412.
Study on Taxol in inhibiting human leukemia cell proliferation and inducing apoptosis
摘要
Objective: To explore the effects of Taxol in inhibiting human leukemia k562 cell proliferation and inducing apoptosis in vitro.Methods: Human leukemia K562 cells were treated with Taxol of different concentrations for 12–72 hrs. Cell proliferation was evaluated by MTT assay and morphological changes of apoptosis were examined by microscopy. Cell apoptosis was determined by flow cytometry (FCM) and DNA gel electrophoresis.Results: Growth of K562 cells was inhibited by Taxol with an IC50 value of 0. 84 ⧎g/ml. Typical nuclear condensation and apoptosis bodies were observed as early as 24 hrs after a 0.5 ⧎g/ml Taxol treatment; Apoptotic rate of the Taxol-treated K562 cells increased from 3.7% to 24.0% in 24 hrs. No DNA ladder was observed by DNA gel electrophoresis.Conclusion: Taxol could inhibit K562 cell growth and induce apoptosis in vitro.
Abstract
Objective: To explore the effects of Taxol in inhibiting human leukemia k562 cell proliferation and inducing apoptosis in vitro.Methods: Human leukemia K562 cells were treated with Taxol of different concentrations for 12–72 hrs. Cell proliferation was evaluated by MTT assay and morphological changes of apoptosis were examined by microscopy. Cell apoptosis was determined by flow cytometry (FCM) and DNA gel electrophoresis.Results: Growth of K562 cells was inhibited by Taxol with an IC50 value of 0. 84 ⧎g/ml. Typical nuclear condensation and apoptosis bodies were observed as early as 24 hrs after a 0.5 ⧎g/ml Taxol treatment; Apoptotic rate of the Taxol-treated K562 cells increased from 3.7% to 24.0% in 24 hrs. No DNA ladder was observed by DNA gel electrophoresis.Conclusion: Taxol could inhibit K562 cell growth and induce apoptosis in vitro.
关键词
TaxolLeukemiaK562 cell linecell apoptosis
Keywords
TaxolLeukemiaK562 cell linecell apoptosis
references
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相关机构
Department of Clinical Molecular Genetics, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences
National Therapeutic Center of Hematology of Traditional Chinese Medicine, Xiyuan Hospital, China Academy of Chinese Medical Sciences
Department of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences
Department of Nephrology, Second Affiliated Hospital of Medical School of Xi’an Jiaotong University
School of Public Health of Xi’an Jiaotong University