Literature DB >> 12628742

The ASPP family: deciding between life and death after DNA damage.

Elizabeth A Slee1, Xin Lu.   

Abstract

It is well established that p53 is a primary target for mutation in human cancer. p53 carries out the important task of ensuring that damaged DNA is not passed on during cell division, a duty that it performs by either inhibiting the cell cycle or inducing apoptosis. However, it is unclear how this decision is made. The recent identification of the ASPP family of proteins, which act to direct the cell away from cell cycle arrest and towards death following p53 upregulation, may explain how this dilemma is resolved. Furthermore, the observation that ASPP2 is in fact the full length form of the previously identified 53BP2/Bbp protein has clarified the ambiguous data that has been generated in relation to this molecule. The further characterisation of these proteins will enable us to gain further insights into the response of the cell to DNA damage and the progression of the cell towards malignancy.

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Year:  2003        PMID: 12628742     DOI: 10.1016/s0378-4274(02)00421-6

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  14 in total

1.  PP1 cooperates with ASPP2 to dephosphorylate and activate TAZ.

Authors:  Chen-Ying Liu; Xianbo Lv; Tingting Li; Yanping Xu; Xin Zhou; Shimin Zhao; Yue Xiong; Qun-Ying Lei; Kun-Liang Guan
Journal:  J Biol Chem       Date:  2010-12-28       Impact factor: 5.157

2.  RNA interference-mediated silencing of iASPP induces cell proliferation inhibition and G0/G1 cell cycle arrest in U251 human glioblastoma cells.

Authors:  Guilin Li; Renzhi Wang; Jun Gao; Kan Deng; Junji Wei; Yanping Wei
Journal:  Mol Cell Biochem       Date:  2010-12-24       Impact factor: 3.396

3.  Mechanisms of regulatory diversity within the p53 transcriptional network.

Authors:  J M Espinosa
Journal:  Oncogene       Date:  2008-02-18       Impact factor: 9.867

4.  Molecular basis of the interaction between the antiapoptotic Bcl-2 family proteins and the proapoptotic protein ASPP2.

Authors:  Chen Katz; Hadar Benyamini; Shahar Rotem; Mario Lebendiker; Tsafi Danieli; Anat Iosub; Hadar Refaely; Monica Dines; Vered Bronner; Tsafrir Bravman; Deborah E Shalev; Stefan Rüdiger; Assaf Friedler
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-21       Impact factor: 11.205

5.  Differential regulation of p53 target genes: it's (core promoter) elementary.

Authors:  Nathan P Gomes; Joaquín M Espinosa
Journal:  Genes Dev       Date:  2010-01-15       Impact factor: 11.361

6.  In vitro effect of iASPP on cell growth of oral tongue squamous cell carcinoma.

Authors:  Yu Chen; Wangxiang Yan; Shuqi He; Jiechun Chen; Dan Chen; Zhaoqiang Zhang; Zhiguo Liu; Xueqiang Ding; Anxun Wang
Journal:  Chin J Cancer Res       Date:  2014-08       Impact factor: 5.087

Review 7.  Restoring p53 tumor suppressor activity as an anticancer therapeutic strategy.

Authors:  Jesse D Martinez
Journal:  Future Oncol       Date:  2010-12       Impact factor: 3.404

8.  ASPP2 is a haploinsufficient tumor suppressor that cooperates with p53 to suppress tumor growth.

Authors:  Virginie Vives; Jian Su; Shan Zhong; Indrika Ratnayaka; Elizabeth Slee; Robert Goldin; Xin Lu
Journal:  Genes Dev       Date:  2006-05-15       Impact factor: 11.361

9.  p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels.

Authors:  N Gopalakrishna Iyer; Suet-Feung Chin; Hilal Ozdag; Yataro Daigo; De-En Hu; Massimiliano Cariati; Kevin Brindle; Samuel Aparicio; Carlos Caldas
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-27       Impact factor: 11.205

10.  A p53-derived apoptotic peptide derepresses p73 to cause tumor regression in vivo.

Authors:  Helen S Bell; Christine Dufes; Jim O'Prey; Diane Crighton; Daniele Bergamaschi; Xin Lu; Andreas G Schätzlein; Karen H Vousden; Kevin M Ryan
Journal:  J Clin Invest       Date:  2007-03-08       Impact factor: 14.808

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