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Updated: May 13, 2026

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
Published on: May 14, 2016
Treat cancers by targeting survivin: just a dream or future reality?
Mohane Selvaraj Coumar1, Fang-Ying Tsai, Jagat Rakesh Kanwar
1Centre for Bioinformatics, School of Life Sciences, Pondicherry University, Kalapet, Puducherry, India.
Abstract:
Since the discovery of survivin (BIRC5) as a cancer-related molecule by Grazia Ambrosini and Dario C. Altieri at 1997, our knowledge related to the function of this molecule has been extended from simple apoptosis inhibition to complicated, interlinked processes that involve interference of mitosis, apoptosis, autophagy, and even DNA repair recently. However, despite the growing amount of knowledge related to survivin in the last ten years, the development of survivin inhibitors or survivin-related molecular therapies is surprisingly and relatively slow as compared to other therapeutic inhibitors for cancer treatment. Here, the molecular functions of survivin and the progress of development of survivin-targeting therapies are discussed in detail. Functional differences between different survivin-specific inhibitors are discussed from both structural and biochemical point of views. This review also reveals different challenges that scientists are currently facing in the development of survivin inhibitors for clinical application. Finally, future directions for the development of survivin-targeted therapies are discussed in this review.
Insights
Survivin (BIRC5) is a key cancer molecule involved in cell division and death. Despite its known functions, developing survivin inhibitors for cancer therapy has been slow, facing significant challenges.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Survivin (BIRC5) discovered in 1997, initially known for apoptosis inhibition.
- Its functions now encompass mitosis, autophagy, and DNA repair, highlighting complex roles in cancer.
Purpose of the Study:
- To review the molecular functions of survivin.
- To discuss the progress and challenges in developing survivin-targeting therapies.
- To explore future directions for survivin inhibitor development.
Main Methods:
- Literature review of survivin's molecular functions.
- Analysis of survivin inhibitor development progress.
- Discussion of structural and biochemical differences between inhibitors.
- Identification of challenges in clinical application.
Main Results:
- Survivin's functions are more complex than initially understood, involving multiple cellular processes.
- Survivin inhibitor development has lagged behind other cancer therapies.
- Various survivin inhibitors exhibit distinct structural and biochemical properties.
Conclusions:
- Despite extensive knowledge of survivin's roles, clinical translation of survivin inhibitors remains a challenge.
- Further research is needed to overcome hurdles in developing effective survivin-targeted therapies.
- Future strategies may focus on novel inhibitor designs and overcoming resistance mechanisms.
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