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Article: Hypocrellin B Enhances Ultrasound-Induced Cell Death of Nasopharyngeal Carcinoma Cells

TitleHypocrellin B Enhances Ultrasound-Induced Cell Death of Nasopharyngeal Carcinoma Cells
Authors
KeywordsApoptosis
Hypocrellin
Nasopharyngeal carcinoma
Necrosis
Sonodynamic therapy
Issue Date2010
Citation
Ultrasound in Medicine and Biology, 2010, v. 36, n. 2, p. 336-342 How to Cite?
AbstractHypocrellin B, a natural pigment from a traditional Chinese herb, has been attracting extensive attention. The present study aims to investigate whether hypocrellin B can enhance cell death induced by ultrasound sonification on nasopharyngeal carcinoma cells in vitro. The sonodynamic action of hypocrellin B was investigated on nasopharyngeal carcinoma cell line CNE2 cells as tumor model cells. In the experiments, the hypocrellin B concentration was kept constant at 2.5 μM and the cells were subject to ultrasound exposure for 15 s at an intensity of 0.65 W/cm2. Cytotoxicity was investigated 24 h after ultrasound sonification. Apoptosis was evaluated using flow cytometry with annexin V-FITC and propidium iodine staining and nuclear staining with Hoechst 33258. Cell ultrastructure morphology was observed using transmission electron microscopy (TEM). No significant dark cytotoxicity of hypocrellin B in the CNE2 cells was observed at the concentration of 2.5 μM. The cell death rate induced by ultrasound sonification was significantly higher in the presence of hypocrellin B than in the absence of hypocrellin B. Flow cytometry showed that ultrasound exposure in the presence of hypocrellin B significantly increased the early and late apoptotic rate, 18.64% and 22.57%, respectively, compared with the controls. Nuclear condensation was observed in the nuclear staining and swollen mitochondria and more vacuolar and broken cell membrane were found in TEM after the treatment of hypocrellin B and ultrasound. Our findings demonstrated that the presence of hypocrellin B significantly enhanced the cytotoxicity of ultrasound radiation in CNE2 cells, suggesting that hypocrellin B is a novel sonosensitizer and hypocrellin B-mediated sonodynamic therapy is a potential therapeutic modality in the management of malignant tumors. (E-mail: xcshan@163.com or awnleung@cuhk.edu.hk). © 2010 World Federation for Ultrasound in Medicine & Biology.
Persistent Identifierhttp://hdl.handle.net/10722/335741
ISSN
2021 Impact Factor: 3.694
2020 SCImago Journal Rankings: 0.893

 

DC FieldValueLanguage
dc.contributor.authorWang, Ping-
dc.contributor.authorXu, Chuan shan-
dc.contributor.authorXu, Jing-
dc.contributor.authorWang, Xinna-
dc.contributor.authorLeung, Albert Wingnang-
dc.date.accessioned2023-12-28T08:48:25Z-
dc.date.available2023-12-28T08:48:25Z-
dc.date.issued2010-
dc.identifier.citationUltrasound in Medicine and Biology, 2010, v. 36, n. 2, p. 336-342-
dc.identifier.issn0301-5629-
dc.identifier.urihttp://hdl.handle.net/10722/335741-
dc.description.abstractHypocrellin B, a natural pigment from a traditional Chinese herb, has been attracting extensive attention. The present study aims to investigate whether hypocrellin B can enhance cell death induced by ultrasound sonification on nasopharyngeal carcinoma cells in vitro. The sonodynamic action of hypocrellin B was investigated on nasopharyngeal carcinoma cell line CNE2 cells as tumor model cells. In the experiments, the hypocrellin B concentration was kept constant at 2.5 μM and the cells were subject to ultrasound exposure for 15 s at an intensity of 0.65 W/cm2. Cytotoxicity was investigated 24 h after ultrasound sonification. Apoptosis was evaluated using flow cytometry with annexin V-FITC and propidium iodine staining and nuclear staining with Hoechst 33258. Cell ultrastructure morphology was observed using transmission electron microscopy (TEM). No significant dark cytotoxicity of hypocrellin B in the CNE2 cells was observed at the concentration of 2.5 μM. The cell death rate induced by ultrasound sonification was significantly higher in the presence of hypocrellin B than in the absence of hypocrellin B. Flow cytometry showed that ultrasound exposure in the presence of hypocrellin B significantly increased the early and late apoptotic rate, 18.64% and 22.57%, respectively, compared with the controls. Nuclear condensation was observed in the nuclear staining and swollen mitochondria and more vacuolar and broken cell membrane were found in TEM after the treatment of hypocrellin B and ultrasound. Our findings demonstrated that the presence of hypocrellin B significantly enhanced the cytotoxicity of ultrasound radiation in CNE2 cells, suggesting that hypocrellin B is a novel sonosensitizer and hypocrellin B-mediated sonodynamic therapy is a potential therapeutic modality in the management of malignant tumors. (E-mail: xcshan@163.com or awnleung@cuhk.edu.hk). © 2010 World Federation for Ultrasound in Medicine & Biology.-
dc.languageeng-
dc.relation.ispartofUltrasound in Medicine and Biology-
dc.subjectApoptosis-
dc.subjectHypocrellin-
dc.subjectNasopharyngeal carcinoma-
dc.subjectNecrosis-
dc.subjectSonodynamic therapy-
dc.titleHypocrellin B Enhances Ultrasound-Induced Cell Death of Nasopharyngeal Carcinoma Cells-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ultrasmedbio.2009.09.007-
dc.identifier.pmid20018428-
dc.identifier.scopuseid_2-s2.0-74849123425-
dc.identifier.volume36-
dc.identifier.issue2-
dc.identifier.spage336-
dc.identifier.epage342-

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