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Original Research Article


Cryptotanshinone Induces Apoptosis of HL-60 Cells via Mitochondrial Pathway

 

Wanmao Ni, Wenbin Qian and Xiangmin Tong

Institute of Hematology, the First Affiliated Hospital, College of Medicine, Zhejiang University, 79# Qingchun Road, Hangzhou 310003, P. R. China

*For correspondence: Email: niwanmao@gmail.com

 

Received: 26 February 2013                                                                  Revised accepted: 12 February 2014

 

Tropical Journal of Pharmaceutical Research, April 2014; 13(4): 545-551

http://dx.doi.org/10.4314/tjpr.v13i4.9   

Abstract

 

Purpose: To test the effect of Cryptotanshinone (CPT), a natural compound isolated from the plant Salvia miltiorrhiza Bunge, on human leukemic cell lines (HL-60).

Methods: HL-60 cells were treated with CPT. Cell growth inhibition (%) was quantitated using MTT assay. Apoptosis detection with Annexin V-FITC/propidium iodide staining was followed by flow cytometry. Caspase-3, caspase-8, and caspase-9 colorimetric assay kit was used to determine caspase protease activity. Loss of mitochondrial membrane potential was examined by flow cytometry with JC-1 staining. Bax, PARP, p53, p21 and cytochrome C were determined using Western blot.

Results: Morphologic assessment, Annexin V-FITC/propidium iodide staining results and sub-G1 percentage indicate that the cytotoxic effect of CPT was mediated by induction of apoptosis. Furthermore, increased Bax expression, decreased Bcl-2 expression, loss of mitochondria membrane potential (MMP), release of cytochrome C, activation of caspase enzyme, cleavage of PARP and accumulation of p53 and p21 were detected during the apoptotic process. Caspase inhibitor partially abrogated CPT-induced apoptosis.

Conclusion: The results show that CPT induced apoptosis of HL-60 cell lines by mitochondria pathway, and suggest that CPT may serve as a potential therapy for leukemia.

 

Keywords: Cryptotanshinone, Salvia miltiorrhiza Bunge, Caspase, Membrane potential, Mitochondrial, Apoptosis, Leukemia, Cytochrome C, Cell cycle.

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