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Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Proliferation-attenuating and apoptosis-inducing effects of tryptanthrin on human chronic myeloid leukemia K562 cell
Shan Miao1, Xiaopeng Shi, Hai Zhang
1Institute of Materia Medica, School of Pharmacy, Fourth Military Medical University, #17 West Changle Road, Xi'an 710032, China; E-Mails: miaoshan@fmmu.edu.cn (S.M.); sunjiy@fmmu.edu.cn (J.S.); miaoqing@fmmu.edu.cn (Q.M.).
Abstract:
Tryptanthrin, a kind of indole quinazoline alkaloid, has been shown to exhibit anti-microbial, anti-inflammation and anti-tumor effects both in vivo and in vitro. However, its biological activity on human chronic myeloid leukemia cell line K562 is not fully understood. In the present study, we investigated the proliferation-attenuating and apoptosis-inducing effects of tryptanthrin on leukemia K562 cells in vitro and explored the underlying mechanisms. The results showed that tryptanthrin could significantly inhibit K562 cells proliferation in a time- and dose-dependent manner as evidenced by MTT assay and flow cytometry analysis. We also observed pyknosis, chromatin margination and the formation of apoptotic bodies in the presence of tryptanthrin under the electron microscope. Nuclei fragmentation and condensation by Hoechst 33258 staining were detected as well. The amount of apoptotic cells significantly increased whereas the mitochondrial membrane potential decreased dramatically after tryptanthrin exposure. K562 cells in the tryptanthrin treated group exhibited an increase in cytosol cyt-c, Bax and activated caspase-3 expression while a decrease in Bcl-2, mito cyt-c and pro-caspase-3 contents. However, the changes of pro-caspase-3 and activated caspase-3 could be abolished by a pan-caspase inhibitor ZVAD-FMK. These results suggest that tryptanthrin has proliferation-attenuating and apoptosis-inducing effects on K562 cells. The underlying mechanism is probably attributed to the reduction in mitochondria membrane potential, the release of mito cyt-c and pro-caspase-3 activation.
Insights
Tryptanthrin significantly inhibits chronic myeloid leukemia K562 cell proliferation and induces apoptosis. This indole alkaloid affects mitochondrial membrane potential and caspase activation, offering potential therapeutic avenues.
Area of Science:
- Pharmacology
- Molecular Biology
- Oncology
Background:
- Tryptanthrin, an indole quinazoline alkaloid, possesses known antimicrobial, anti-inflammatory, and antitumor properties.
- The specific effects of tryptanthrin on human chronic myeloid leukemia (CML) K562 cells remain incompletely characterized.
Purpose of the Study:
- To investigate the antiproliferative and apoptosis-inducing effects of tryptanthrin on K562 cells.
- To elucidate the underlying molecular mechanisms of tryptanthrin's action on leukemia cells.
Main Methods:
- MTT assay and flow cytometry were used to assess cell proliferation and apoptosis.
- Electron microscopy and Hoechst 33258 staining were employed to observe morphological changes.
- Mitochondrial membrane potential, cytochrome c release, and caspase activation (caspase-3) were analyzed.
Main Results:
- Tryptanthrin demonstrated significant, time- and dose-dependent inhibition of K562 cell proliferation.
- Morphological analysis revealed apoptosis, including pyknosis and apoptotic body formation.
- Tryptanthrin induced a decrease in mitochondrial membrane potential, increased cytosolic cytochrome c, and promoted caspase-3 activation, which was reversible with a caspase inhibitor.
Conclusions:
- Tryptanthrin exhibits significant proliferation-attenuating and apoptosis-inducing effects on K562 leukemia cells.
- The mechanism involves mitochondrial dysfunction, cytochrome c release, and caspase-3 activation.
- Tryptanthrin shows potential as a therapeutic agent against chronic myeloid leukemia.
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