Applied Microbiology Research Center, System Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
DNA Repair (Amst). 2021 Jun;102:103103. doi: 10.1016/j.dnarep.2021.103103. Epub 2021 Mar 26.
At the cellular level, DNA repair mechanisms are crucial in maintaining both genomic integrity and stability. DNA damage appears to be a central culprit in tumor onset and progression. Cyclin-dependent kinases (CDKs) and their regulatory partners coordinate the cell cycle progression. Aberrant CDK activity has been linked to a variety of cancers through deregulation of cell-cycle control. Besides DNA damaging agents and chromosome instability (CIN), disruptions in the levels of cell cycle regulators including cyclin-dependent kinase inhibitors (CDKIs) would result in unscheduled proliferation and cell division. The INK4 and Cip/Kip (CDK interacting protein/kinase inhibitor protein) family of CDKI proteins are involved in cell cycle regulation, transcription regulation, apoptosis, and cell migration. A thorough understanding of how these CDKIs regulate the DNA damage response through multiple signaling pathways may provide an opportunity to design efficient treatment strategies to inhibit carcinogenesis.
在细胞水平上,DNA 修复机制对于维持基因组的完整性和稳定性至关重要。DNA 损伤似乎是肿瘤发生和进展的核心罪魁祸首。细胞周期蛋白依赖性激酶(CDKs)及其调节伙伴协调细胞周期的进展。通过细胞周期控制的失调,异常的 CDK 活性与多种癌症有关。除了 DNA 损伤剂和染色体不稳定性(CIN)外,细胞周期调节剂水平的破坏,包括细胞周期蛋白依赖性激酶抑制剂(CDKIs),会导致细胞无计划增殖和分裂。INK4 和 Cip/Kip(CDK 相互作用蛋白/激酶抑制剂蛋白)家族的 CDKIs 蛋白参与细胞周期调控、转录调控、细胞凋亡和细胞迁移。深入了解这些 CDKIs 如何通过多种信号通路调节 DNA 损伤反应,可能为设计有效的治疗策略抑制致癌作用提供机会。