MOLECULAR MECHANISMS REGULATING THE CELL CYCLE AND THEIR SIGNIFICANCE IN PATHOLOGICAL PROCESSES

The cell cycle is a tightly coordinated sequence of events that enables cellular growth, DNA replication, chromosome segregation, and division. Its fidelity depends on cyclin-dependent kinases (CDKs), cyclins, checkpoint proteins, ubiquitin-mediated proteolysis, and DNA-damage response pathways. This narrative review synthesizes established molecular mechanisms governing the G1/S, intra-S, and G2/M transitions and examines their disruption in cancer, developmental disorders, and tissue degeneration. Particular attention is paid to the RB–E2F axis, p53–p21 signaling, ATM/ATR checkpoint pathways, and the anaphase-promoting complex/cyclosome. Understanding these interconnected mechanisms helps explain uncontrolled proliferation, genomic instability, and cellular senescence, while identifying potential therapeutic targets. The review is based on published scientific literature and does not report original experimental results.

Authors

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-10-30
DOI
https://doi.org/10.5281/zenodo.23784378
Primary Topic
Cancer-related Molecular Pathways
Type
article
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article

MOLECULAR MECHANISMS REGULATING THE CELL CYCLE AND THEIR SIGNIFICANCE IN PATHOLOGICAL PROCESSES

Dadajonov Sa'dulla Rafiqjon oʻgʻli
2 links
Zenodo (CERN European Organization for Nuclear Research)
Cancer-related Molecular Pathways
article

MOLECULAR MECHANISMS REGULATING THE CELL CYCLE AND THEIR SIGNIFICANCE IN PATHOLOGICAL PROCESSES

Dadajonov Sa'dulla Rafiqjon oʻgʻli
article en

Abstract

The cell cycle is a tightly coordinated sequence of events that enables cellular growth, DNA replication, chromosome segregation, and division. Its fidelity depends on cyclin-dependent kinases (CDKs), cyclins, checkpoint proteins, ubiquitin-mediated proteolysis, and DNA-damage response pathways. This narrative review synthesizes established molecular mechanisms governing the G1/S, intra-S, and G2/M transitions and examines their disruption in cancer, developmental disorders, and tissue degeneration. Particular attention is paid to the RB–E2F axis, p53–p21 signaling, ATM/ATR checkpoint pathways, and the anaphase-promoting complex/cyclosome. Understanding these interconnected mechanisms helps explain uncontrolled proliferation, genomic instability, and cellular senescence, while identifying potential therapeutic targets. The review is based on published scientific literature and does not report original experimental results.

Zenodo (CERN European Organization for Nuclear Research)
Openalex Percentile: Top 16%
Cancer-related Molecular Pathways
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