O 2 ⋅− and H 2 O 2 -Mediated Disruption of Fe Metabolism Causes the Differential Susceptibility of NSCLC and GBM Cancer Cells to Pharmacological Ascorbate
2017; Cell Press; Volume: 31; Issue: 4 Linguagem: Inglês
10.1016/j.ccell.2017.02.018
ISSN1878-3686
AutoresJoshua D. Schoenfeld, Zita A. Sibenaller, Kranti A. Mapuskar, Brett A. Wagner, Kimberly Cramer-Morales, Muhammad Furqan, Sonia Sandhu, Thomas Carlisle, Mark C. Smith, Taher Abu Hejleh, Daniel Berg, Jun Zhang, John Keech, Kalpaj R. Parekh, Sudershan K. Bhatia, Varun Monga, Kellie L. Bodeker, Logan Ahmann, Sandy Vollstedt, Heather A. Brown, Erin P. Shanahan Kauffman, Mary E. Schall, R.J. Hohl, Gerald H. Clamon, Jeremy D.W. Greenlee, Matthew A. Howard, Michael K. Schultz, Bruce A. Smith, Dennis P. Riley, Frederick E. Domann, Joseph J. Cullen, Garry R. Buettner, John M. Buatti, Douglas R. Spitz, Bryan G. Allen,
Tópico(s)Vitamin D Research Studies
ResumoPharmacological ascorbate has been proposed as a potential anti-cancer agent when combined with radiation and chemotherapy. The anti-cancer effects of ascorbate are hypothesized to involve the autoxidation of ascorbate leading to increased steady-state levels of H
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