Isaria cicadae conidia possess antiproliferative and inducing apoptosis properties in gynaecological carcinoma cells

Isaria cicadae is an entomogenous fungus that has been used as a traditional Chinese medicinal materials to treat different diseases, including cancer. However, Isaria cicadae conidia for inhibitory activity against breast cancer cells growth are still not systematically studied. The present aim was...

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Published inMycology Vol. 8; no. 4; pp. 327 - 334
Main Authors Sun, Yan-fang, Sun, Yang, Wang, Zhi-an, Han, Rui-lian, Lu, Hong-fei, Zhang, Jia-lei, Liu, Hong-tao, Wang, Shi-xian, Wang, Pan, Dian, Lu-lu, Liang, Zong-suo
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 02.10.2017
Taylor & Francis Ltd
Taylor & Francis Group
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Summary:Isaria cicadae is an entomogenous fungus that has been used as a traditional Chinese medicinal materials to treat different diseases, including cancer. However, Isaria cicadae conidia for inhibitory activity against breast cancer cells growth are still not systematically studied. The present aim was to elucidate the phytochemical composition of Isaria cicadae conidia and to explore relevant anti-cancer potential in gynaecological carcinoma MCF-7 and Hela cells. Isaria cicadae conidia were identified by UPLC-ESI-Q-TOF-MS: high performance liquid chromatography-electrospray/quadrupole time of flight tandem mass spectrometry technology. Eight main compounds were identified which are nucleosides, cordycepic acid, cordycepin, beauvericin and myriocin by MS fragmentation ions. The nuclear morphology indicated the typical characteristics of apoptosis by Hoechst staining. Annexin V/PI staining revealed that the number of apoptotic cells was increased by Isaria cicadae conidia treatment. Furthermore, Isaria cicadae conidia also induced the caspase-mediated mitochondrial apoptosis pathway. The findings suggest that the full-scale active ingredients highlight the significance of Isaria cicadae conidia as potential anti-cancer agent in China.
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These authors contributed equally to this work.
ISSN:2150-1203
2150-1211
DOI:10.1080/21501203.2017.1386243