The interplay of transition metals in ferroptosis and
pyroptosis

J 2024

The interplay of transition metals in ferroptosis and pyroptosis

VÁŇA, František, Zoltán SZABÓ, Michal MASAŘÍK and Monika KRATOCHVÍLOVÁ

Basic information

Original name

The interplay of transition metals in ferroptosis and pyroptosis

Authors

VÁŇA, František (203 Czech Republic, belonging to the institution), Zoltán SZABÓ (703 Slovakia, belonging to the institution), Michal MASAŘÍK (203 Czech Republic, belonging to the institution) and Monika KRATOCHVÍLOVÁ (203 Czech Republic, belonging to the institution)

Edition

Cell Division, London, BMC, 2024, 1747-1028

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10608 Biochemistry and molecular biology

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

URL

Impact factor

Impact factor: 2.300 in 2022

Organization unit

Faculty of Medicine

DOI

http://dx.doi.org/10.1186/s13008-024-00127-9

UT WoS

001282976300001

Keywords in English

ferroptosis; pyroptosis; transition metals; interplay

Abstract

V originále

Cell death is one of the most important mechanisms of maintaining homeostasis in our body. Ferroptosis and pyroptosis are forms of necrosis-like cell death. These cell death modalities play key roles in the pathophysiology of cancer, cardiovascular, neurological diseases, and other pathologies. Transition metals are abundant group of elements in all living organisms. This paper presents a summary of ferroptosis and pyroptosis pathways and their connection to significant transition metals, namely zinc (Zn), copper (Cu), molybdenum (Mo), lead (Pb), cobalt (Co), iron (Fe), cadmium (Cd), nickel (Ni), mercury (Hg), uranium (U), platinum (Pt), and one crucial element, selenium (Se). Authors aim to summarize the up-to-date knowledge of this topic. In this review, there are categorized and highlighted the most common patterns in the alterations of ferroptosis and pyroptosis by transition metals. Special attention is given to zinc since collected data support its dual nature of action in both ferroptosis and pyroptosis. All findings are presented together with a brief description of major biochemical pathways involving mentioned metals and are visualized in attached comprehensive figures. This work concludes that the majority of disruptions in the studied metals’ homeostasis impacts cell fate, influencing both death and survival of cells in the complex system of altered pathways. Therefore, this summary opens up the space for further research.

Links

MUNI/A/1547/2023, interní kód MU

Name: Analýza (dys)funkce: od molekul k živému organismu

Investor: Masaryk University, Analysis of (dys)function: from molecules to the living organism

MUNI/A/1587/2023, interní kód MU

Name: Patofyziologie vybraných komplexních nemocí od molekulární do systémovou úroveň

Investor: Masaryk University, Pathophysiology of selected complex diseases from molecular to systemic level

Citovat

VÁŇA, František, Zoltán SZABÓ, Michal MASAŘÍK and Monika KRATOCHVÍLOVÁ. The interplay of transition metals in ferroptosis and pyroptosis. Cell Division. London: BMC, 2024, vol. 19, No 1, p. 1-26. ISSN 1747-1028. Available from: https://dx.doi.org/10.1186/s13008-024-00127-9.

@article{2422317,
   author = {Váňa, František and Szabó, Zoltán and Masařík, Michal and Kratochvílová, Monika},
   article_location = {London},
   article_number = {1},
   doi = {http://dx.doi.org/10.1186/s13008-024-00127-9},
   keywords = {ferroptosis; pyroptosis; transition metals; interplay},
   language = {eng},
   issn = {1747-1028},
   journal = {Cell Division},
   title = {The interplay of transition metals in ferroptosis and pyroptosis},
   url = {https://celldiv.biomedcentral.com/articles/10.1186/s13008-024-00127-9},
   volume = {19},
   year = {2024}
}

TY  - JOUR
ID  - 2422317
AU  - Váňa, František - Szabó, Zoltán - Masařík, Michal - Kratochvílová, Monika
PY  - 2024
TI  - The interplay of transition metals in ferroptosis and pyroptosis
JF  - Cell Division
VL  - 19
IS  - 1
SP  - 1-26
EP  - 1-26
PB  - BMC
SN  - 17471028
KW  - ferroptosis
KW  - pyroptosis
KW  - transition metals
KW  - interplay
UR  - https://celldiv.biomedcentral.com/articles/10.1186/s13008-024-00127-9
N2  - Cell death is one of the most important mechanisms of maintaining homeostasis in our body. Ferroptosis and pyroptosis are forms of necrosis-like cell death. These cell death modalities play key roles in the pathophysiology of cancer, cardiovascular, neurological diseases, and other pathologies. Transition metals are abundant group of elements in all living organisms. This paper presents a summary of ferroptosis and pyroptosis pathways and their connection to significant transition metals, namely zinc (Zn), copper (Cu), molybdenum (Mo), lead (Pb), cobalt (Co), iron (Fe), cadmium (Cd), nickel (Ni), mercury (Hg), uranium (U), platinum (Pt), and one crucial element, selenium (Se). Authors aim to summarize the up-to-date knowledge of this topic. In this review, there are categorized and highlighted the most common patterns in the alterations of ferroptosis and pyroptosis by transition metals. Special attention is given to zinc since collected data support its dual nature of action in both ferroptosis and pyroptosis. All findings are presented together with a brief description of major biochemical pathways involving mentioned metals and are visualized in attached comprehensive figures. This work concludes that the majority of disruptions in the studied metals’ homeostasis impacts cell fate, influencing both death and survival of cells in the complex system of altered pathways. Therefore, this summary opens up the space for further research.
ER  -

VÁŇA, František, Zoltán SZABÓ, Michal MASAŘÍK and Monika KRATOCHVÍLOVÁ. The interplay of transition metals in ferroptosis and pyroptosis. \textit{Cell Division}. London: BMC, 2024, vol.~19, No~1, p.~1-26. ISSN~1747-1028. Available from: https://dx.doi.org/10.1186/s13008-024-00127-9.

Detailed Information on Publication Record