期刊论文详细信息
BMC Complementary and Alternative Medicine
Antiproliferative activity and induction of apoptotic by ethanolic extract of Alpinia galanga rhizhome in human breast carcinoma cell line
Mohadeseh Hosseini2  Jalil Tavakkol Afshari4  Mousa-Al-Reza Hadjzadeh1  Saeed Samarghandian3 
[1] Department of Physiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran;Department of Biology, Payame Nour University of Tehran, Tehran, Iran;Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran;Immunogentics and Cell Culture Department, Immunology Research Center, Bu-Ali Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran
关键词: MTT;    MRC-5;    MCF-7;    Cytotoxicity;    Alpinia galanga L;   
Others  :  1220092
DOI  :  10.1186/1472-6882-14-192
 received in 2013-06-18, accepted in 2014-05-08,  发布年份 2014
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【 摘 要 】

Background

We investigated the potential of galangal rhizomes to induce cytotoxic and apoptotic effects in the cultured human breast carcinoma cell line, (MCF-7) in compare with the non-malignant (MRC-5) cells.

Methods

Both cells were cultured in DMEM medium and treated with galangal rhizomes for three consecutive days. The percentage of apoptotic cells was determined by flow cytometry using Annexin-V fluorescein isothiocyanate.

Results

The results showed that the ethanolic extract of galangal rhizomes decreased cell viability in the malignant cells as a concentration- and time- dependent manner. The IC50 values against MCF-7 were determined at 400.0 ± 11.7 and 170.0 ± 5.9 μg/ml after 48 and 72 h respectively. The morphology of MCF-7 cells treated with the ethanolic extract confirmed the cell proliferation assay results. Alpinia galanga induced apoptosis in MCF-7 cells, as determined by flow cytometry.

Conclusions

We concluded that the extract of Alpinia galanga exerts pro-apoptotic effects in a breast cancer-derived cell line and could be considered as a potential chemotherapeutic agent in breast cancer.

【 授权许可】

   
2014 Samarghandian et al.; licensee BioMed Central Ltd.

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