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Updated: Jun 29, 2026

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
Published on: May 14, 2016
Cancer therapy: targeting cell cycle regulators
Martin Johansson1, Jenny Liao Persson
1Department of Laboratory Medicine, Lund University, Malmö University Hospital, 205 02, Malmö, Sweden.
Abstract:
Cyclins and CDKs play critical roles in DNA synthesis and cell division. Alterations in their function may lead to the disruption of normal cell growth and apoptosis, and subsequently, result in carcinogenesis. Elevated levels of cyclins and CDKs are frequently observed in a wide range of different types of human cancers. Understanding of molecular mechanisms underlying the cell cycle effects in response to the chemotherapeutic agents is of great importance for improving the efficacy of targeted therapeutics and overcoming resistance to chemotherapeutic agents. Despite the clinical applications of cell cycle specific chemotherapeutic agents, there is still an urgent need to develop novel drugs that can target multiple sites and pathways of the cell cycle while avoiding drug induced cytotoxicity. In this review article, we will summarize the development of novel agents that specifically target cell cycle pathways in human cancer. We will discuss drugs that can directly interfere with the mitotic process of tumor cells. Moreover, we tend to address the significance of using small molecule CDK inhibitors that are derived from natural products.
Insights
Novel agents targeting cell cycle pathways offer new hope for cancer treatment. This review explores drugs that interfere with tumor cell mitosis and highlights natural product-derived cyclin-dependent kinase (CDK) inhibitors.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Cyclins and cyclin-dependent kinases (CDKs) regulate DNA synthesis and cell division.
- Dysregulation of cell cycle control is a hallmark of cancer, often involving elevated cyclins and CDKs.
- Understanding cell cycle response to chemotherapy is crucial for enhancing treatment efficacy and overcoming resistance.
Purpose of the Study:
- To review the development of novel therapeutic agents targeting cell cycle pathways in human cancers.
- To discuss drugs that directly inhibit tumor cell mitosis.
- To highlight the potential of small molecule CDK inhibitors derived from natural products.
Main Methods:
- Literature review of recent advancements in cell cycle-targeted cancer therapeutics.
- Analysis of drug mechanisms interfering with mitotic processes.
- Exploration of natural product-derived compounds as CDK inhibitors.
Main Results:
- Elevated cyclins and CDKs are common in various human cancers.
- Novel agents are being developed to target specific cell cycle pathways.
- Natural products show promise as sources for small molecule CDK inhibitors.
Conclusions:
- Targeting cell cycle pathways presents a promising strategy for cancer therapy.
- Developing drugs that inhibit mitosis and utilize natural product-derived CDK inhibitors can improve treatment outcomes.
- Further research is needed to overcome drug-induced cytotoxicity and resistance.
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