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DOI 10.3109/15376516.2015.1045656

Медицинская библиотека · Toxicology mechanisms and methods · 2015

Cell cycle arrest and apoptogenic properties of opium alkaloids noscapine and papaverine on breast cancer stem cells.

Sajadian Saharolsadat, Vatankhah Melody, Majdzadeh Maryam, Kouhsari Shide Montaser, Ghahremani Mohammad Hossein, Ostad Seyed Nasser

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Previous report of the vast effectiveness of opium derivatives in cancer therapy is leading us to see possible effects of these derivatives on cancer stem cells in order to find new agent for cancer therapy. In this study, cells were stained for CSC markers and sorted by magnetic beads. CSCs exhibit the characteristic CD44(+)/CD24(-/low)/ESA(+) phenotype. Noscapine and papaverine (alkaloids) showed anti-proliferative activity on MCF-7 and MDA-MB-231 cell lines. It was observed that noscapine has more cytotoxic effect on CSC derived from both cell lines compared with their parental cells. Papaverine has more cytotoxic effect on MCF-7 CSCs in comparison with parental cells, while CSCs population of MDA-MB-231 is more resistant to papaverine compared with MDA-MB-231 cells. Noscapine enhances apoptosis in MDA-MB-231 CSCs more than parent cells, while in MCF-7 CSCs the apoptosis is less than parent cells. Our results show that papverine is less active in terms of apoptotic effect on CSCs in both cell lines. Moreover, noscapine arrests MCF-7 and MDA-MB-231 CSCs cell cycle at G2/M phase, while papverine arrests cell cycle at G0/G1 phase. It was suggested different mechanism for apoptotic cytotoxicity. The results of this study show possible specific effects of noscapine on these breast cell lines CSCs.

Для цитирования: Sajadian Saharolsadat, Vatankhah Melody, Majdzadeh Maryam, Kouhsari Shide Montaser, Ghahremani Mohammad Hossein, Ostad Seyed Nasser. Cell cycle arrest and apoptogenic properties of opium alkaloids noscapine and papaverine on breast cancer stem cells.. Toxicology mechanisms and methods. 2015. DOI: 10.3109/15376516.2015.1045656.

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