Immunogenic cell death-inducing Rh(i) and Ir(i) complexes with bis(imino)acenaphthene-derived ligands: insights into the role of the metal center and the ligands; Inorganic Chemistry Frontiers; Vol. 13, iss. 2

Bibliografiske detaljer
Parent link:Inorganic Chemistry Frontiers.— .— London: Royal Society of Chemistry
Vol. 13, iss. 2.— 2026.— P. 403-419
Andre forfattere: Chengnan Wu, Romashev N. F. Nikolai, Komlyagina V. Veronika, Petrović T. Tamara, Bakaev I. V. Ivan, Abramov P. A. Pavel Aleksandrovich, Yuan Wang, Ryadun A. A. Alexey, Fomenko I. S. Iakov, Taotao Zou, Gushchin A. L. Artem, Babak M. V. Maria
Summary:Title screen
While various metal complexes demonstrate immunogenic cell death (ICD)-inducing properties, there is a lack of studies comparing ICD properties in structurally similar complexes with different metal centers. In this study, we synthesized four structurally similar Rh(I) and Ir(I) complexes with redox-active 1,2-bis(arylimino)acenaphthene (Ar-bian) ligands and assessed their anticancer and ICD-inducing properties. Analysis of damage-associated molecular patterns (DAMPs), ROS localization and dying cell populations highlighted the distinct roles of the metal center and the ligands. Specifically, only Rh(I) complexes induced the release of the three essential DAMPs and high levels of late apoptotic cells, while the Ir(I) complexes failed to trigger crucial “eat-me” signals. This work offers valuable insights into structure–activity relationships in metal complexes in the context of ICD
Текстовый файл
AM_Agreement
Sprog:engelsk
Udgivet: 2026
Fag:
Online adgang:https://doi.org/10.1039/D5QI00868A
Format: Electronisk Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=685896

MARC

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330 |a While various metal complexes demonstrate immunogenic cell death (ICD)-inducing properties, there is a lack of studies comparing ICD properties in structurally similar complexes with different metal centers. In this study, we synthesized four structurally similar Rh(I) and Ir(I) complexes with redox-active 1,2-bis(arylimino)acenaphthene (Ar-bian) ligands and assessed their anticancer and ICD-inducing properties. Analysis of damage-associated molecular patterns (DAMPs), ROS localization and dying cell populations highlighted the distinct roles of the metal center and the ligands. Specifically, only Rh(I) complexes induced the release of the three essential DAMPs and high levels of late apoptotic cells, while the Ir(I) complexes failed to trigger crucial “eat-me” signals. This work offers valuable insights into structure–activity relationships in metal complexes in the context of ICD 
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