Survivin and Tumorigenesis: Molecular Mechanisms and Therapeutic Strategies

Xun Chen1, Ning Duan1, Caiguo Zhang2

  • 11. Hong-Hui Hospital, Xi'an Jiaotong University, College of Medicine, Xi'an, Shaanxi, China, 710054.

Journal of Cancer
|February 27, 2016
PubMed

Insights

Survivin, a key protein in cell division and apoptosis, is highly expressed in cancers. Understanding its molecular basis and targeting it offers potential therapeutic strategies for various cancers.

Area of Science:

  • Molecular Biology
  • Cancer Biology
  • Biochemistry

Background:

  • Survivin is the smallest inhibitor of apoptosis protein (IAP), crucial for cell division and apoptosis inhibition by blocking caspase activation.
  • Elevated survivin expression is observed in numerous human cancers, including lung, pancreatic, and breast cancers, compared to normal tissues.
  • Aberrant survivin expression correlates with increased tumor cell proliferation, progression, angiogenesis, therapeutic resistance, and poorer patient prognosis.

Purpose of the Study:

  • To review recent advancements in understanding the molecular mechanisms of survivin.
  • To summarize preclinical therapeutic strategies targeting survivin.

Main Methods:

  • Literature review of studies on survivin's molecular basis.
  • Compilation of data on survivin's role in signaling pathways.
  • Summary of preclinical therapeutic approaches targeting survivin.

Main Results:

  • Survivin regulates cytokinesis and cell cycle progression.
  • Survivin interacts with multiple signaling pathways, including p53, Wnt, hypoxia, transforming growth factor, and Notch.
  • Preclinical studies show promise for survivin-targeted therapies.

Conclusions:

  • Survivin's multifaceted roles in cancer necessitate further investigation.
  • Targeting survivin presents a viable strategy for cancer therapy development.

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