Repression of the Antiapoptotic Molecule Galectin-3 by Homeodomain-Interacting Protein Kinase 2-Activated p53 Is Required for p53-Induced Apoptosis

Author:

Cecchinelli Barbara1,Lavra Luca23,Rinaldo Cinzia1,Iacovelli Stefano1,Gurtner Aymone1,Gasbarri Alessandra4,Ulivieri Alessandra23,Del Prete Fabrizio4,Trovato Maria5,Piaggio Giulia1,Bartolazzi Armando46,Soddu Silvia1,Sciacchitano Salvatore237

Affiliation:

1. Department of Experimental Oncology, Regina Elena Cancer Institute, 00158 Rome, Italy

2. S. Pietro Fatebenefratelli Hospital-Associazione Fatebenefratelli per la Ricerca, 00189 Rome, Italy

3. Department of Experimental Medicine and Pathology, II Faculty of Medicine, University “La Sapienza,”

4. Department of Pathology, Sant'Andrea Hospital, 00189 Rome, Italy

5. Department of Human Pathology, University of Messina, 98100 Messina, Italy

6. Cellular and Molecular Tumor Pathology Laboratory, Cancer Center Karolinska, Karolinska Hospital, Stockholm, Sweden

7. Institute of Neurobiology, Experimental and Molecular Medicine, Centro Nazionale Ricerche, Rome, Italy

Abstract

ABSTRACT Galectin 3 (Gal-3), a member of the β-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.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference61 articles.

1. Akahani, S., P. Nangia-Makker, H. Inohara, H.-R. Kim, and A. Raz. 1997. Galectin-3: a novel antiapoptotic molecule with a functional BH1 (NWGR) domain of Bcl-2 family. Cancer Res.57:5272-5276.

2. Appella, E., and C. W. Anderson. 2000. Signaling to p53: breaking the post-translational modification code. Pathol. Biol.48:227-245.

3. Regulation of p53 Function and Stability by Phosphorylation

4. Bacchetti, S., and F. Graham. 1993. Inhibition of cell proliferation by an adenovirus vector expressing the human wild type p53 protein. Int. J. Oncol.3:781-788.

5. Barondes, S. H., V. Castronovo, D. N. Cooper, R. D. Cummings, K. Drickamer, T. Feizi, M. A. Gitt, J. Hirabayashi, C. Hughes, K. Kasai, et al. 1994. Galectins: a family of animal beta-galactoside-binding lectins. Cell76:597-598.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3