Literature DB >> 16377176

Specific peptides for the therapeutic targeting of oncogenes.

Gilbert G Privé1, Ari Melnick.   

Abstract

Tumors are dependent on oncogenic proteins for their maintenance and survival. The ideal cancer therapy would include drugs that specifically target these proteins. Many such proteins function through interfaces that can be difficult to target effectively with small molecules. However, recent advances in cell-permeable peptide technology, improving cellular penetration and stability, raise the possibility that specific peptide interference of oncogenic proteins could be successfully translated to the clinic. Several active anti-tumor peptides were recently described. For example, a stable peptide inhibitor of the Hsp90 ATP-binding pocket killed a wide range of tumors in vitro and in vivo, and a peptide inhibitor of the BCL6 oncoprotein was active in B-cell lymphomas; both peptides functioned without toxicity to normal tissues.

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Year:  2005        PMID: 16377176     DOI: 10.1016/j.gde.2005.12.010

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  9 in total

Review 1.  Evolution: a guide to perturb protein function and networks.

Authors:  Olivier Lichtarge; Angela Wilkins
Journal:  Curr Opin Struct Biol       Date:  2010-05-03       Impact factor: 6.809

2.  Sequential transcription factor targeting for diffuse large B-cell lymphomas.

Authors:  Leandro C Cerchietti; Jose M Polo; Gustavo F Da Silva; Pedro Farinha; Rita Shaknovich; Randy D Gascoyne; Steven F Dowdy; Ari Melnick
Journal:  Cancer Res       Date:  2008-05-01       Impact factor: 12.701

Review 3.  Therapeutic targeting of the BCL6 oncogene for diffuse large B-cell lymphomas.

Authors:  Samir Parekh; Gilbert Privé; Ari Melnick
Journal:  Leuk Lymphoma       Date:  2008-05

4.  Molecular decoy to the Y-box binding protein-1 suppresses the growth of breast and prostate cancer cells whilst sparing normal cell viability.

Authors:  Jennifer H Law; Yvonne Li; Karen To; Michelle Wang; Arezoo Astanehe; Karen Lambie; Jaspreet Dhillon; Steven J M Jones; Martin E Gleave; Connie J Eaves; Sandra E Dunn
Journal:  PLoS One       Date:  2010-09-10       Impact factor: 3.240

5.  Blockade of CD40-TRAF2,3 or CD40-TRAF6 is sufficient to inhibit pro-inflammatory responses in non-haematopoietic cells.

Authors:  Jose-Andres C Portillo; Jennifer A Greene; Isaac Schwartz; Maria Cecilia Subauste; Carlos S Subauste
Journal:  Immunology       Date:  2015-01       Impact factor: 7.397

6.  Characterizing the role of Hsp90 in production of heat shock proteins in motor neurons reveals a suppressive effect of wild-type Hsf1.

Authors:  David M Taylor; Miranda L Tradewell; Sandra Minotti; Heather D Durham
Journal:  Cell Stress Chaperones       Date:  2007       Impact factor: 3.667

7.  A cell-penetrating CD40-TRAF2,3 blocking peptide diminishes inflammation and neuronal loss after ischemia/reperfusion.

Authors:  Jose-Andres C Portillo; Jin-Sang Yu; Samuel Hansen; Timothy S Kern; M Cecilia Subauste; Carlos S Subauste
Journal:  FASEB J       Date:  2021-03       Impact factor: 5.191

8.  Transtactin: a universal transmembrane delivery system for Strep-tag II-fused cargos.

Authors:  Markus A Moosmeier; Julia Bulkescher; Jennifer Reed; Martina Schnölzer; Hans Heid; Karin Hoppe-Seyler; Felix Hoppe-Seyler
Journal:  J Cell Mol Med       Date:  2009-07-07       Impact factor: 5.310

9.  The Spectrum of Design Solutions for Improving the Activity-Selectivity Product of Peptide Antibiotics against Multidrug-Resistant Bacteria and Prostate Cancer PC-3 Cells.

Authors:  Davor Juretić; Anja Golemac; Denise E Strand; Keshi Chung; Nada Ilić; Ivana Goić-Barišić; François-Xavier Pellay
Journal:  Molecules       Date:  2020-08-01       Impact factor: 4.411

  9 in total

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