Literature DB >> 25688111

Arginine methyltransferases as novel therapeutic targets for breast cancer.

Alan Morettin1, R Mitchell Baldwin1, Jocelyn Côté2.   

Abstract

Breast cancer is the most commonly diagnosed female cancer in the world. Though therapeutic treatments are available to treat breast cancer and in some instances are successful, the occurrence of unsuccessful treatment, or the rate of tumour recurrence, still remains strikingly high. Therefore, novel therapeutic treatment targets need to be discovered and tested. The protein arginine methyltransferases (PRMTs) are a family of enzymes that catalyse arginine methylation and are implicated in a myriad of cellular pathways including transcription, DNA repair, RNA metabolism, signal transduction, protein-protein interactions and subcellular localisation. In breast cancer, the expression levels and enzymatic activity of a number of PRMTs is dysregulated; significantly altering the regulation of many cellular pathways that are implicated in breast cancer development and progression. Here, we review the current knowledge on PRMTs in breast cancer and provide a rationale for how PRMTs may provide novel therapeutic targets for the treatment of breast cancer.
© The Author 2015. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Year:  2015        PMID: 25688111     DOI: 10.1093/mutage/geu039

Source DB:  PubMed          Journal:  Mutagenesis        ISSN: 0267-8357            Impact factor:   3.000


  19 in total

1.  Islet-specific Prmt5 excision leads to reduced insulin expression and glucose intolerance in mice.

Authors:  Jian Ma; Xin He; Yan Cao; Kienan O'Dwyer; Katherine M Szigety; Yuan Wu; Buddha Gurung; Zijie Feng; Bryson W Katona; Xianxin Hua
Journal:  J Endocrinol       Date:  2020-01-01       Impact factor: 4.286

2.  Transition state mimics are valuable mechanistic probes for structural studies with the arginine methyltransferase CARM1.

Authors:  Matthijs J van Haren; Nils Marechal; Nathalie Troffer-Charlier; Agostino Cianciulli; Gianluca Sbardella; Jean Cavarelli; Nathaniel I Martin
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-22       Impact factor: 11.205

3.  Hijacking DNA methyltransferase transition state analogues to produce chemical scaffolds for PRMT inhibitors.

Authors:  Ludovic Halby; Nils Marechal; Dany Pechalrieu; Vincent Cura; Don-Marc Franchini; Céline Faux; Fréderic Alby; Nathalie Troffer-Charlier; Srikanth Kudithipudi; Albert Jeltsch; Wahiba Aouadi; Etienne Decroly; Jean-Claude Guillemot; Patrick Page; Clotilde Ferroud; Luc Bonnefond; Dominique Guianvarc'h; Jean Cavarelli; Paola B Arimondo
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-06-05       Impact factor: 6.237

4.  Arginine methylation of translocated in liposarcoma (TLS) inhibits its binding to long noncoding RNA, abrogating TLS-mediated repression of CBP/p300 activity.

Authors:  Wei Cui; Ryoma Yoneda; Naomi Ueda; Riki Kurokawa
Journal:  J Biol Chem       Date:  2018-05-21       Impact factor: 5.157

5.  Mouse Models of Overexpression Reveal Distinct Oncogenic Roles for Different Type I Protein Arginine Methyltransferases.

Authors:  Jianqiang Bao; Alessandra Di Lorenzo; Kevin Lin; Yue Lu; Yi Zhong; Manu M Sebastian; William J Muller; Yanzhong Yang; Mark T Bedford
Journal:  Cancer Res       Date:  2018-10-23       Impact factor: 12.701

6.  LKB1 regulates PRMT5 activity in breast cancer.

Authors:  Hanine Lattouf; Loay Kassem; Julien Jacquemetton; Ali Choucair; Coralie Poulard; Olivier Trédan; Laura Corbo; Mona Diab-Assaf; Nader Hussein; Isabelle Treilleux; Muriel Le Romancer
Journal:  Int J Cancer       Date:  2018-10-31       Impact factor: 7.396

Review 7.  Biological chemistry and functionality of protein sulfenic acids and related thiol modifications.

Authors:  Nelmi O Devarie-Baez; Elsa I Silva Lopez; Cristina M Furdui
Journal:  Free Radic Res       Date:  2015-11-11

8.  Global mapping of CARM1 substrates defines enzyme specificity and substrate recognition.

Authors:  Evgenia Shishkova; Hao Zeng; Fabao Liu; Nicholas W Kwiecien; Alexander S Hebert; Joshua J Coon; Wei Xu
Journal:  Nat Commun       Date:  2017-05-24       Impact factor: 14.919

9.  PRMT1-mediated methylation of MICU1 determines the UCP2/3 dependency of mitochondrial Ca(2+) uptake in immortalized cells.

Authors:  Corina T Madreiter-Sokolowski; Christiane Klec; Warisara Parichatikanond; Sarah Stryeck; Benjamin Gottschalk; Sergio Pulido; Rene Rost; Emrah Eroglu; Nicole A Hofmann; Alexander I Bondarenko; Tobias Madl; Markus Waldeck-Weiermair; Roland Malli; Wolfgang F Graier
Journal:  Nat Commun       Date:  2016-09-19       Impact factor: 14.919

10.  Tudor Domain Containing Protein 3 Promotes Tumorigenesis and Invasive Capacity of Breast Cancer Cells.

Authors:  Alan Morettin; Geneviève Paris; Younes Bouzid; R Mitchell Baldwin; Theresa J Falls; John C Bell; Jocelyn Côté
Journal:  Sci Rep       Date:  2017-07-11       Impact factor: 4.379

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