Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71349
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dc.contributor.authorIsara Phiwchaien_US
dc.contributor.authorTitipun Thongtemen_US
dc.contributor.authorSomchai Thongtemen_US
dc.contributor.authorChalermchai Pilapongen_US
dc.date.accessioned2021-01-27T03:41:02Z-
dc.date.available2021-01-27T03:41:02Z-
dc.date.issued2020-01-01en_US
dc.identifier.issn15590283en_US
dc.identifier.issn10859195en_US
dc.identifier.other2-s2.0-85092550295en_US
dc.identifier.other10.1007/s12013-020-00951-0en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85092550295&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/71349-
dc.description.abstract© 2020, Springer Science+Business Media, LLC, part of Springer Nature. Herein, we studied the effect of labile iron (ferric chloride) on the progression of liver cancer cells (HepG2.2.15). The iron was found to induce cell proliferation, growth, and migration in both traditional two-dimensional (2D) and three-dimensional cell (3D) culture models. Biophysical and cell cycle determinations also showed the change in functional cellular biophysical features (cell morphology) and cell cycle kinetic during cancer cell growth induced by the labile iron. According to immunofluorescence and the iron uptake inhibition studies, L-type calcium channel was found to plays a role in the iron uptake in the liver cancer cells. This report gives new insights into iron-mediated cancer cell growth and will pave the new way to diagnosis and treatment of liver cancer.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleLiver Cancer Cells Uptake Labile Iron via L-type Calcium Channel to Facilitate the Cancer Cell Proliferationen_US
dc.typeJournalen_US
article.title.sourcetitleCell Biochemistry and Biophysicsen_US
article.stream.affiliationsChiang Mai Universityen_US
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