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Updated: May 10, 2026

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
Published on: May 14, 2016
Mitosis as an anti-cancer drug target
Anna-Leena Salmela1, Marko J Kallio
1VTT Biotechnology for Health and Wellbeing, VTT Technical Research Centre of Finland, Itäinen Pitkäkatu 4C, Pharmacity Bldg, 4th Floor, P.O. Box 106, 20521, Turku, Finland.
Abstract:
Suppression of cell proliferation by targeting mitosis is one potential cancer intervention. A number of existing chemotherapy drugs disrupt mitosis by targeting microtubule dynamics. While efficacious, these drugs have limitations, i.e. neuropathy, unpredictability and development of resistance. In order to overcome these issues, a great deal of effort has been spent exploring novel mitotic targets including Polo-like kinase 1, Aurora kinases, Mps1, Cenp-E and KSP/Eg5. Here we summarize the latest developments in the discovery and clinical evaluation of new mitotic drug targets.
Insights
Targeting cell division (mitosis) offers a cancer treatment strategy. Researchers are exploring new drugs that target mitotic proteins to overcome limitations of current therapies like neuropathy and resistance.
Area of Science:
- Oncology
- Cell Biology
- Pharmacology
Background:
- Targeting mitosis is a key strategy in cancer therapy.
- Current microtubule-targeting chemotherapy drugs have significant limitations, including neuropathy and drug resistance.
- Novel mitotic targets are needed to improve cancer treatment efficacy and safety.
Purpose of the Study:
- To review the latest advancements in novel mitotic drug targets for cancer intervention.
- To summarize the discovery and clinical evaluation of new therapeutic targets in mitosis.
Main Methods:
- Literature review of recent research on mitotic targets.
- Analysis of clinical trial data for novel mitotic inhibitors.
- Summary of drug discovery efforts for specific mitotic kinases and proteins.
Main Results:
- Several novel mitotic targets, including Polo-like kinase 1 (PLK1), Aurora kinases, Mps1, Cenp-E, and KSP/Eg5, are under investigation.
- Early clinical evaluations show promise for some of these new targets.
- Identification of potential biomarkers for patient stratification is ongoing.
Conclusions:
- Novel mitotic targets represent a promising avenue for developing more effective and less toxic cancer therapies.
- Continued research and clinical evaluation are crucial for translating these discoveries into clinical practice.
- Targeting specific mitotic pathways may overcome resistance mechanisms associated with traditional chemotherapy.
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