Literature DB >> 14646536

BAG-1 inhibits p53-induced but not apoptin-induced apoptosis.

A A Danen-van Oorschot1, A I den Hollander, S Takayama, J C Reed, A J van der Eb, M H Noteborn.   

Abstract

BAG-1 has been identified as a Bcl-2-binding protein that inhibits apoptosis, either alone or in co-operation with Bcl-2. Here we show that BAG-1 inhibits p53- induced apoptosis in the human tumour cell line Saos-2. In contrast, BAG-1 was unable to inhibit the p53-independent pathway induced by apoptin, an apoptosis-inducing protein derived from chicken anaemia virus. Whereas BAG-1 seemed to co-operate with Bcl-2 to repress p53-induced apoptosis, co-expression of these proteins had no inhibitory effect on apoptin-induced apoptosis. Moreover, Bcl-2, and to some extent also BAG-1, paradoxically enhanced the apoptotic activity of apoptin. These results demonstrate that p53 and apoptin induce apoptosis through independent pathways, which are differentially regulated by BAG-1 and Bcl-2.

Entities:  

Year:  1997        PMID: 14646536     DOI: 10.1023/a:1026409808732

Source DB:  PubMed          Journal:  Apoptosis        ISSN: 1360-8185            Impact factor:   4.677


  3 in total

1.  The chicken anemia virus-derived protein apoptin requires activation of caspases for induction of apoptosis in human tumor cells.

Authors:  A A Danen-van Oorschot; A J van Der Eb; M H Noteborn
Journal:  J Virol       Date:  2000-08       Impact factor: 5.103

2.  The BAG-1 cochaperone is a negative regulator of p73-dependent transcription.

Authors:  X-H Wang; D O'Connor; M Brimmell; G Packham
Journal:  Br J Cancer       Date:  2009-03-17       Impact factor: 7.640

3.  λ Phage nanobioparticle expressing apoptin efficiently suppress human breast carcinoma tumor growth in vivo.

Authors:  Alireza Shoae-Hassani; Peyman Keyhanvar; Alexander Marcus Seifalian; Seyed Abdolreza Mortazavi-Tabatabaei; Narmin Ghaderi; Khosro Issazadeh; Nour Amirmozafari; Javad Verdi
Journal:  PLoS One       Date:  2013-11-22       Impact factor: 3.240

  3 in total

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