Litcius/Paper detail

Mitochondria-dependent ferroptosis plays a pivotal role in doxorubicin cardiotoxicity

Tomonori Tadokoro, Masataka Ikeda, Tomomi Ide, Hiroko Deguchi, Soichiro Ikeda, Kosuke Okabe, Akihito Ishikita, Shouji Matsushima, Tomoko Koumura, Ken‐ichi Yamada, Hirotaka Imai, Hiroyuki Tsutsui

2023JCI Insight80 citationsDOIOpen Access PDF

Abstract

The authors recently became aware that the Mito-FerroGreen (MFG) used in this study is not an Fe 2+ chelator, but instead reduces Fe 2+ via conversion to Fe 3+ .As MFG mediates reduction of Fe 2+ and suppresses ferroptosis, the overall conclusions are not affected.For clarity, the authors have removed references to MFG-mediated chelation throughout, updated the Graphical Abstract, and renumbered the reference list to refer to Hirayama et al. ( 1) when first describing the use of MFG in the Results section.The text and Graphical Abstract have been updated in the HTML version and PDF.The Journal has also published an online version of the original article with the incorrect statements crossed out and

Topics & Concepts

CardiotoxicityDoxorubicinMitochondrionCancer researchChemistryCell biologyPharmacologyMedicineInternal medicineBiologyBiochemistryChemotherapyFerroptosis and cancer prognosis
Mitochondria-dependent ferroptosis plays a pivotal role in doxorubicin cardiotoxicity | Litcius