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.

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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