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Usage Information

Reawakening the cellular death program in neoplasia through the therapeutic blockade of IAP function
Casey W. Wright, Colin S. Duckett
Casey W. Wright, Colin S. Duckett
Published October 3, 2005
Citation Information: J Clin Invest. 2005;115(10):2673-2678. https://doi.org/10.1172/JCI26251.
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Review Series

Reawakening the cellular death program in neoplasia through the therapeutic blockade of IAP function

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Abstract

Recent studies have shown that members of the inhibitor of apoptosis (IAP) protein family are highly expressed in several classes of cancer. The primary implication of these findings is that the elevated expression of IAPs is not coincidental but actually participates in oncogenesis by helping to allow the malignant cell to avoid apoptotic cell death. This concept, together with the discovery of several IAP-regulatory proteins that use a conserved mode of action, has stimulated a major effort by many research groups to devise IAP-targeting strategies as a means of developing novel antineoplastic drugs. In this Review, we consider the evidence both for and against the IAPs being valid therapeutic targets, and we describe the types of strategies being used to neutralize their functions.

Authors

Casey W. Wright, Colin S. Duckett

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Usage data is cumulative from May 2024 through May 2025.

Usage JCI PMC
Text version 752 20
PDF 65 20
Figure 175 6
Citation downloads 72 0
Totals 1,064 46
Total Views 1,110
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Usage information is collected from two different sources: this site (JCI) and Pubmed Central (PMC). JCI information (compiled daily) shows human readership based on methods we employ to screen out robotic usage. PMC information (aggregated monthly) is also similarly screened of robotic usage.

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