Scinovex
reviewTop 1% cited

Survivin: Key Regulator of Mitosis and Apoptosis and Novel Target for Cancer Therapeutics

Clinical Cancer Research · 2008 · Vol. 14(16) · pp. 5000–5005
Alain C. MitaMonica MitaSteffan T. NawrockiFrancis J. Giles

Abstract

Survivin, a member of the family of inhibitor of apoptosis proteins, functions as a key regulator of mitosis and programmed cell death. Initially, survivin was described as an inhibitor of caspase-9. However, over the last years, research studies have shown that the role of survivin in cancer pathogenesis is not limited to apoptosis inhibition but also involves the regulation of the mitotic spindle checkpoint and the promotion of angiogenesis and chemoresistance. Survivin gene expression is transcriptionally repressed by wild-type p53 and can be deregulated in cancer by several mechanisms, including gene amplification, hypomethylation, increased promoter activity, and loss of p53 function. This article reviews the multiple functions of survivin in the regulation of apoptosis, the promotion of tumorigenesis, and the development of survivin inhibitors as a novel anticancer therapeutic strategy.

Cell death mechanisms and regulationCancer-related Molecular PathwaysMicrotubule and mitosis dynamicsSurvivinCancer researchMitosisRegulatorApoptosisInhibitor of apoptosisCarcinogenesisBiologyCancer cellCancer

MeSH terms

SurvivinAnimalsAntineoplastic AgentsHumansMicrotubule-Associated ProteinsMitosisNeoplasm ProteinsNeoplasmsSignal TransductionApoptosisInhibitor of Apoptosis Proteins
Citations
779
FWCI
22.21
field-weighted impact
References
88
Percentile
100%
vs. same field & year
Citations per year
References
Life-or-death decisions by the Bcl-2 protein family
Trends in Biochemical Sciences · 2001 · 882 citations
The Hallmarks of Cancer
Cell · 2000 · 28,385 citations
BCL-2 family members and the mitochondria in apoptosis
Genes & Development · 1999 · 3,645 citations
IAP family proteins---suppressors of apoptosis
Genes & Development · 1999 · 2,549 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.