Selective inhibition of proteins regulating CDK/cyclin complexes: strategy against cancer--a review
P Sarita Rajender1, D Ramasree, K Bhargavi
1Department of Chemistry, Nizam College, Basheerbagh, Hyderabad, Andhra Pradesh, India.
Abstract:
Cancer prevention is a global priority, but history indicates that the journey towards achieving the goal is difficult. Various cyclin dependent kinase complexes (CDKs/cyclins) operate as major cell signaling components in all stages of cell cycle. CDK/cyclin protein complexes, regulating the cell cycle, are conserved during evolution. In cancer cells, cell division is uncontrolled and CDKs/cyclins become 'check-points' or targets. Keeping this in view the proteins cyclin C, cyclin D2, CDKN1C, and Growth Arrest and DNA Damage (GADD45alpha) which play a major role in regulating CDK/cyclin complexes and operate in the initial stages of cell cycle (G(0) phase-S phase), have been identified as promising targets. Targeting critical regulators of cell-cycle signaling components by applying modern computational techniques is projected to be a potential tool for future cancer research.
Insights
Targeting cell cycle regulators like cyclin C and CDKN1C offers a promising strategy for cancer prevention. Computational methods can identify critical targets in cell cycle signaling for future cancer research.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cancer prevention is a global health priority, yet achieving this goal remains challenging.
- Cyclin-dependent kinase (CDK)/cyclin complexes are crucial regulators of the cell cycle, conserved across evolution.
- Uncontrolled cell division in cancer cells highlights CDKs/cyclins as critical targets.
Purpose of the Study:
- To identify key proteins involved in regulating CDK/cyclin complexes at the G(0)-S phase transition.
- To explore the potential of targeting these regulators for cancer research and prevention.
Main Methods:
- Identification of specific proteins: cyclin C, cyclin D2, CDKN1C, and Growth Arrest and DNA Damage (GADD45alpha).
- Focus on proteins regulating CDK/cyclin complexes in early cell cycle stages.
- Application of modern computational techniques for target identification.
Main Results:
- Cyclin C, cyclin D2, CDKN1C, and GADD45alpha identified as significant regulators of CDK/cyclin complexes.
- These proteins play a major role in the G(0) to S phase transition of the cell cycle.
- Computational approaches are highlighted as valuable tools for discovering cancer targets.
Conclusions:
- Targeting specific CDK/cyclin regulators like cyclin C, cyclin D2, CDKN1C, and GADD45alpha presents a promising avenue for cancer prevention.
- Modern computational techniques are essential for identifying and validating critical targets in cell cycle signaling pathways.
- This research provides a foundation for developing novel therapeutic strategies against cancer.
Related Concept Videos
Inhibition of Cdk Activity
Inhibition of CDK Activity
M-Cdk Drives Transition Into Mitosis
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Positive Regulator Molecules
Positive Regulator Molecules
Targeted Cancer Therapies
There are several types of targeted therapies against specific...


