Literature DB >> 29057043

Resorcinol-Based Grp94-Selective Inhibitors.

Anuj Khandelwal1, Vincent M Crowley1, Brian S J Blagg2.   

Abstract

Glucose regulated protein 94 (Grp94) is the endoplasmic reticulum resident of the 90 kDa heat shock protein (Hsp90) family and represents a promising therapeutic target for the treatment of several diseases. Grp94 is the most unique member of the 90 kDa heat shock protein family due to a five amino acid insertion into its primary sequence, which creates hydrophobic subpockets exclusive to Grp94 that can be utilized for selective inhibition. The first resorcinol-based Grp94-selective inhibitor to take advantage of the hydrophobic S2 subpocket has been developed and shown to manifest low nanomolar affinity and ∼10-fold selectivity for Grp94. Furthermore, these Grp94-selective inhibitors manifest low micromolar GI50 values against multiple myeloma cells, supporting Grp94 as an emerging target for the treatment of this disease.

Entities:  

Keywords:  Grp94; Heat shock protein 90; cancer; multiple myeloma

Year:  2017        PMID: 29057043      PMCID: PMC5641966          DOI: 10.1021/acsmedchemlett.7b00193

Source DB:  PubMed          Journal:  ACS Med Chem Lett        ISSN: 1948-5875            Impact factor:   4.345


  32 in total

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Review 2.  Glucose-regulated proteins in cancer: molecular mechanisms and therapeutic potential.

Authors:  Amy S Lee
Journal:  Nat Rev Cancer       Date:  2014-04       Impact factor: 60.716

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Journal:  Hum Mol Genet       Date:  2014-07-15       Impact factor: 6.150

4.  Development of radamide analogs as Grp94 inhibitors.

Authors:  Aaron Muth; Vincent Crowley; Anuj Khandelwal; Sanket Mishra; Jinbo Zhao; Jessica Hall; Brian S J Blagg
Journal:  Bioorg Med Chem       Date:  2014-06-12       Impact factor: 3.641

5.  Structure-guided development of specific pyruvate dehydrogenase kinase inhibitors targeting the ATP-binding pocket.

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Journal:  J Biol Chem       Date:  2013-12-19       Impact factor: 5.157

Review 6.  Targeting the dynamic HSP90 complex in cancer.

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Journal:  Nat Rev Cancer       Date:  2010-08       Impact factor: 60.716

7.  Molecular chaperone gp96 is a novel therapeutic target of multiple myeloma.

Authors:  Yunpeng Hua; Shai White-Gilbertson; Joshua Kellner; Saleh Rachidi; Saad Z Usmani; Gabriela Chiosis; Ronald Depinho; Zihai Li; Bei Liu
Journal:  Clin Cancer Res       Date:  2013-09-27       Impact factor: 12.531

8.  Experimental and structural testing module to analyze paralogue-specificity and affinity in the Hsp90 inhibitors series.

Authors:  Tony Taldone; Pallav D Patel; Maulik Patel; Hardik J Patel; Christopher E Evans; Anna Rodina; Stefan Ochiana; Smit K Shah; Mohammad Uddin; Daniel Gewirth; Gabriela Chiosis
Journal:  J Med Chem       Date:  2013-08-21       Impact factor: 7.446

9.  Transformation of the Non-Selective Aminocyclohexanol-Based Hsp90 Inhibitor into a Grp94-Seletive Scaffold.

Authors:  Sanket J Mishra; Suman Ghosh; Andrew R Stothert; Chad A Dickey; Brian S J Blagg
Journal:  ACS Chem Biol       Date:  2016-12-13       Impact factor: 5.100

Review 10.  Hallmarks of cancer: the next generation.

Authors:  Douglas Hanahan; Robert A Weinberg
Journal:  Cell       Date:  2011-03-04       Impact factor: 41.582

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Review 2.  Molecular Chaperones in Cancer Stem Cells: Determinants of Stemness and Potential Targets for Antitumor Therapy.

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4.  Evaluation of [11C]NMS-E973 as a PET tracer for in vivo visualisation of HSP90.

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Journal:  Theranostics       Date:  2019-01-01       Impact factor: 11.556

Review 5.  Inhibitors of the Plasmodium falciparum Hsp90 towards Selective Antimalarial Drug Design: The Past, Present and Future.

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Review 6.  Cancer drug resistance: rationale for drug delivery systems and targeted inhibition of HSP90 family proteins.

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Review 7.  Cell Surface GRP94 as a Novel Emerging Therapeutic Target for Monoclonal Antibody Cancer Therapy.

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