J 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:

URL

Organization

Lékařská fakulta – Repository – Repository

DOI

http://dx.doi.org/10.1080/13510002.2024.2371173

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.
Displayed: 18/7/2025 23:00