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001-es BibID:	BIBFORM083079
035-os BibID:	(cikkazonosító)860 (WoS)000497971600005 (Scopus)85074933970
Első szerző:	Molnár Tamás (molekuláris biológus)
Cím:	Current translational potential and underlying molecular mechanisms of necroptosis / Molnár Tamás, Mázló Anett, Tslaf Vera, Szöllősi Attila Gábor, Emri Gabriella, Koncz Gábor
Dátum:	2019
ISSN:	2041-4889
Megjegyzések:	Cell death has a fundamental impact on the evolution of degenerative disorders, autoimmune processes, inflammatory diseases, tumor formation and immune surveillance. Over the past couple of decades extensive studies have uncovered novel cell death pathways, which are independent of apoptosis. Among these is necroptosis, a tightly regulated, inflammatory form of cell death. Necroptosis contribute to the pathogenesis of many diseases and in this review, we will focus exclusively on necroptosis in humans. Necroptosis is considered a backup mechanism of apoptosis, but the in vivo appearance of necroptosis indicates that both caspase-mediated and caspase-independent mechanisms control necroptosis. Necroptosis is regulated on multiple levels, from the transcription, to the stability and posttranslational modifications of the necrosome components, to the availability of molecular interaction partners and the localization of receptor-interacting serine/threonine-protein kinase 1 (RIPK1), receptor-interacting serine/threonine-protein kinase 3 (RIPK3) and mixed lineage kinase domain-like protein (MLKL). Accordingly, we classified the role of more than seventy molecules in necroptotic signaling based on consistent in vitro or in vivo evidence to understand the molecular background of necroptosis and to find opportunities where regulating the intensity and the modality of cell death could be exploited in clinical interventions. Necroptosis specific inhibitors are under development, but >20 drugs, already used in the treatment of various diseases, have the potential to regulate necroptosis. By listing necroptosis-modulated human diseases and cataloging the currently available drug-repertoire to modify necroptosis intensity, we hope to kick-start approaches with immediate translational potential. We also indicate where necroptosis regulating capacity should be considered in the current applications of these drugs
Tárgyszavak:	Természettudományok Biológiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban folyóiratcikk
Megjelenés:	Cell Death & Disease. - 10 : 11 (2019), p. 1-21. -
További szerzők:	Türk-Mázló Anett (1989-) (molekuláris biológus) Tslaf Vera Szöllősi Attila Gábor (1982-) (élettanász) Emri Gabriella (1972-) (bőrgyógyász, allergológus, onkológus) Koncz Gábor (1970-) (biológus, immunológus)
Pályázati támogatás:	125224 OTKA 2.3.2-15-2016-00005 GINOP 128034 NKFIH 125224 NKIFH ÚNKP-18-3 Egyéb ÚNKP19-4-DE-142 Egyéb
Internet cím:	Szerző által megadott URL DOI Intézményi repozitóriumban (DEA) tárolt változat
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001-es BibID:	BIBFORM101734
035-os BibID:	(cikkazonosító)423 (WoS)000789850400001 (Scopus)85129238146
Első szerző:	Türk-Mázló Anett (molekuláris biológus)
Cím:	Types of necroinflammation, the effect of cell death modalities on sterile inflammation / Anett Mázló, Viktória Jenei, Sára Burai, Tamás Molnár, Attila Bácsi, Gábor Koncz
Dátum:	2022
Megjegyzések:	Distinct types of immune responses are activated by infections, which cause the development of type I, II, or III inflammation, regulated by Th1, Th2, Th17 helper T cells and ILC1, ILC2 and ILC3 cells, respectively. While the classification of immune responses to different groups of pathogens is widely accepted, subtypes of the immune response elicited by sterile inflammation have not yet been detailed. Necroinflammation is associated with the release of damage-associated molecular patterns (DAMP) from dying cells. In this review, we present that the distinct molecular mechanisms activated during apoptosis, necroptosis, pyroptosis, and ferroptosis lead to the release of different patterns of DAMPs and their suppressors, SAMPs. We summarize the currently available data on how regulated cell death pathways and released DAMPs and SAMPs direct the differentiation of T helper and ILC cells. Understanding the subtypes of necroinflammation can be crucial in developing strategies for the treatment of sterile inflammatory diseases caused by cell death processes.
Tárgyszavak:	Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban folyóiratcikk Inflammasome Necroptosis
Megjelenés:	Cell Death and Disease. - 13 : 5 (2022), p. 1-12. -
További szerzők:	Jenei Viktória (1997-) (biológus) Burai Sára (1998-) (immunológus) Molnár Tamás (1989-) (molekuláris biológus) Bácsi Attila (1967-) (immunológus) Koncz Gábor (1970-) (biológus, immunológus)
Internet cím:	Szerző által megadott URL DOI Intézményi repozitóriumban (DEA) tárolt változat
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