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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao The Prostatearrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
The Prostate
Article . 2002 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
The Prostate
Article . 2002
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Inhibitors of apoptosis proteins in prostate cancer cell lines

Authors: Kevin R, McEleny; R William G, Watson; Ronan N T, Coffey; Amanda J, O'Neill; John M, Fitzpatrick;

Inhibitors of apoptosis proteins in prostate cancer cell lines

Abstract

AbstractBACKGROUNDThe caspases are the central executioners of apoptosis. The inhibitors of apoptosis proteins (IAPs) are a family of recently described caspase inhibitors. We hypothesised that tumor resistance to apoptosis could be due in part to IAP expression.METHODSThe expression of NAIP, cIAP‐1, cIAP‐2, XIAP, and survivin was investigated in the prostate cancer cell lines LNCaP, PC3, and DU145. RNase protection assays and Western blotting were used to assess RNA and protein expression. Apoptotic susceptibility was determined using etoposide and assessed by propidium iodide (PI) DNA incorporation using flow cytometry.RESULTSDU145 and PC3 cells were more resistant to apoptosis than LNCaP cells. All the IAPs were identified in the cell lines with variation in IAP expression between different cell types. Immunohistochemistry demonstrated cIAP‐1 expression in PC3 cells was nuclear, while the expression of cIAP‐2 and XIAP was perinuclear. Growing LNCaP cells in charcoal‐stripped or androgen‐supplemented medium resulted in no alteration in IAP expression.CONCLUSIONSThis study characterises the expression of IAP in three of the most commonly used prostate cancer cells. IAP may make an important contribution to apoptotic resistance in patients with prostate cancer. Prostate 51: 133–140, 2002. © 2002 Wiley‐Liss, Inc.

Keywords

Male, Chromosomal Proteins, Non-Histone, Survivin, Prostatic Neoplasms, Proteins, Apoptosis, Nerve Tissue Proteins, X-Linked Inhibitor of Apoptosis Protein, Cysteine Proteinase Inhibitors, Immunohistochemistry, Neuronal Apoptosis-Inhibitory Protein, Inhibitor of Apoptosis Proteins, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, Protein Biosynthesis, Tumor Cells, Cultured, Humans, Enzyme Inhibitors, Microtubule-Associated Proteins

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
103
Top 10%
Top 10%
Top 1%
Related to Research communities
Cancer Research
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