TY - JOUR
T1 - Lysosomal lipid peroxidation contributes to ferroptosis induction via lysosomal membrane permeabilization
AU - Saimoto, Yuma
AU - Kusakabe, Daiki
AU - Morimoto, Kazushi
AU - Matsuoka, Yuta
AU - Kozakura, Eisho
AU - Kato, Nao
AU - Tsunematsu, Kayoko
AU - Umeno, Tomohiro
AU - Kiyotani, Tamiko
AU - Matsumoto, Shota
AU - Tsuji, Mieko
AU - Hirayama, Tasuku
AU - Nagasawa, Hideko
AU - Uchida, Koji
AU - Karasawa, Satoru
AU - Jutanom, Mirinthorn
AU - Yamada, Ken Ichi
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Ferroptosis, a form of cell death instigated by iron-dependent lipid peroxidation reactions (LPO), is emerging as a promising therapeutic target for cancer. While the mechanisms governing LPO induction and suppression have gradually been unveiled, questions persist regarding the specific cellular location of LPO and the utilization of iron in driving cell death. A comprehensive understanding of these aspects holds significant potential for advancing therapeutic applications in disease management. Here, we show lysosomal LPO in the initiation of ferroptosis, leveraging the hidden abilities of fluorescent detection probes. Intra-lysosomal LPO triggers iron leakage, fostering cell-wide LPO by augmenting lysosomal membrane permeabilization (LMP). Conversely, cell lines with low susceptibility to ferroptosis do not exhibit LMP. This deficiency is rectified by the concurrent administration of chloroquine, leading to LMP induction and subsequent cell death. These findings underscore enhancing LMP induction efficacy as a strategic approach to surmount resistance to therapies in cancer.
AB - Ferroptosis, a form of cell death instigated by iron-dependent lipid peroxidation reactions (LPO), is emerging as a promising therapeutic target for cancer. While the mechanisms governing LPO induction and suppression have gradually been unveiled, questions persist regarding the specific cellular location of LPO and the utilization of iron in driving cell death. A comprehensive understanding of these aspects holds significant potential for advancing therapeutic applications in disease management. Here, we show lysosomal LPO in the initiation of ferroptosis, leveraging the hidden abilities of fluorescent detection probes. Intra-lysosomal LPO triggers iron leakage, fostering cell-wide LPO by augmenting lysosomal membrane permeabilization (LMP). Conversely, cell lines with low susceptibility to ferroptosis do not exhibit LMP. This deficiency is rectified by the concurrent administration of chloroquine, leading to LMP induction and subsequent cell death. These findings underscore enhancing LMP induction efficacy as a strategic approach to surmount resistance to therapies in cancer.
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U2 - 10.1038/s41467-025-58909-w
DO - 10.1038/s41467-025-58909-w
M3 - Article
C2 - 40229298
AN - SCOPUS:105002983957
SN - 2041-1723
VL - 16
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 3554
ER -