Repression of the antiapoptotic molecule galectin-3 by homeodomain-interacting protein kinase 2-activated p53 is required for p53-induced apoptosis

被引:87
作者
Cecchinelli, Barbara
Lavra, Luca
Rinaldo, Cinzia
Iacovelli, Stefano
Gurtner, Aymone
Gasbarri, Alessandra
Ulivieri, Alessandra
Del Prete, Fabrizio
Trovato, Maria
Piaggio, Giulia
Bartolazzi, Armando
Soddu, Silvia
Sciacchitano, Salvatore
机构
[1] Sant Andrea Hosp, Dept Pathol, I-00189 Rome, Italy
[2] Regina Elena Inst Canc Res, Dept Expt Oncol, I-00158 Rome, Italy
[3] S Pietro Fatebenefratelli Hosp Assoc Fatebenefrat, I-00189 Rome, Italy
[4] Univ Messina, Dept Human Pathol, I-98100 Messina, Italy
[5] Karolinska Hosp, Canc Ctr Karolinska, Cellular & Mol Tumor Pathol Lab, S-10401 Stockholm, Sweden
[6] Univ Roma La Sapienza, Fac Med 2, Dept Expt Med & Pathol, Rome, Italy
[7] CNR, Inst Neurobiol Expt & Mol Med, Rome, Italy
关键词
D O I
10.1128/MCB.00959-05
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Galectin 3 (Gal-3), a member of the beta-galactoside binding lectin family, exhibits antiapoptotic functions, and its aberrant expression is involved in various aspects of tumor progression. Here we show that p53-induced apoptosis is associated with transcriptional repression of Gal-3. Previously, it has been reported that phosphorylation of p53 at Ser46 is important for transcription of proapoptotic genes and induction of apoptosis and that homeodomain-interacting protein kinase 2 (HIPK2) is specifically involved in these functions. We show that HIPK2 cooperates with p53 in Gal-3 repression and that this cooperation requires HIPK2 kinase activity. Gene-specific RNA interference demonstrates that HIPK2 is essential for repression of Gal-3 upon induction of p53-dependent apoptosis. Furthermore, expression of a nonrepressible Gal-3 prevents HIPK2- and p53-induced apoptosis. These results reveal a new apoptotic pathway induced by HIPK2-activated p53 and requiring repression of the antiapoptotic factor Gal-3.
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收藏
页码:4746 / 4757
页数:12
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