Přehled o publikaci
2024
Navigating the redox landscape: reactive oxygen species in regulation of cell cycle
MACKOVÁ, Viktória; Martina RAUDENSKÁ; Hana HOLCOVÁ POLANSKÁ; Milan JAKUBEK; Michal MASAŘÍK et. al.Basic information
Original name
Navigating the redox landscape: reactive oxygen species in regulation of cell cycle
Authors
MACKOVÁ, Viktória; Martina RAUDENSKÁ; Hana HOLCOVÁ POLANSKÁ; Milan JAKUBEK and Michal MASAŘÍK
Edition
Redox Report, ABINGDON, FRANCIS LTD, 2024, 1351-0002
Other information
Language
English
Type of outcome
Article in a journal
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
is not subject to a state or trade secret
References:
Organization
Lékařská fakulta – Repository – Repository
UT WoS
001263591500001
EID Scopus
2-s2.0-85197666848
Keywords in English
cell cycle; reactive oxygen species; oxidative stress; proliferation; redox state; redox-sensitive targets; cell cycle signaling
Links
LX22NPO5102, research and development project. MUNI/A/1587/2023, interní kód Repo.
Changed: 2/8/2024 00:50, RNDr. Daniel Jakubík
Abstract
V originále
Objectives: To advance our knowledge of disease mechanisms and therapeutic options, understanding cell cycle regulation is critical. Recent research has highlighted the importance of reactive oxygen species (ROS) in cell cycle regulation. Although excessive ROS levels can lead to age-related pathologies, ROS also play an essential role in normal cellular functions. Many cell cycle regulatory proteins are affected by their redox status, but the precise mechanisms and conditions under which ROS promote or inhibit cell proliferation are not fully understood. Methods: This review presents data from the scientific literature and publicly available databases on changes in redox state during the cell cycle and their effects on key regulatory proteins. Results: We identified redox-sensitive targets within the cell cycle machinery and analysed different effects of ROS (type, concentration, duration of exposure) on cell cycle phases. For example, moderate levels of ROS can promote cell proliferation by activating signalling pathways involved in cell cycle progression, whereas excessive ROS levels can induce DNA damage and trigger cell cycle arrest or cell death. Discussion: Our findings encourage future research focused on identifying redox-sensitive targets in the cell cycle machinery, potentially leading to new treatments for diseases with dysregulated cell proliferation.