Literature DB >> 16250907

Proteasome inhibitors as therapeutics.

Constantine S Mitsiades1, Nicholas Mitsiades, Teru Hideshima, Paul G Richardson, Kenneth C Anderson.   

Abstract

The ubiquitin-proteasome pathway is a principle intracellular mechanism for controlled protein degradation and has recently emerged as an attractive target for anticancer therapies, because of the pleiotropic cell-cycle regulators and modulators of apoptosis that are controlled by proteasome function. In this chapter, we review the current state of the field of proteasome inhibitors and their prototypic member, bortezomib, which was recently approved by the U.S. Food and Drug Administration for the treatment of advanced multiple myeloma. Particular emphasis is placed on the pre-clinical research data that became the basis for eventual clinical applications of proteasome inhibitors, an overview of the clinical development of this exciting drug class in multiple myeloma, and a appraisal of possible uses in other haematological malignancies, such non-Hodgkin's lymphomas.

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Year:  2005        PMID: 16250907     DOI: 10.1042/EB0410205

Source DB:  PubMed          Journal:  Essays Biochem        ISSN: 0071-1365            Impact factor:   8.000


  14 in total

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Authors:  Michael Hopfner; Detlef Schuppan; Hans Scherubl
Journal:  World J Gastroenterol       Date:  2008-12-14       Impact factor: 5.742

Review 2.  Treatment of gastrointestinal neuroendocrine tumors with inhibitors of growth factor receptors and their signaling pathways: recent advances and future perspectives.

Authors:  Michael Höpfner; Detlef Schuppan; Hans Scherübl
Journal:  World J Gastroenterol       Date:  2008-04-28       Impact factor: 5.742

3.  Small molecule anti-angiogenic probes of the ubiquitin proteasome pathway: potential application to choroidal neovascularization.

Authors:  Paola Bargagna-Mohan; Padma Priya Ravindranath; Royce Mohan
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-09       Impact factor: 4.799

4.  The casein kinase I protein Cck1 regulates multiple signaling pathways and is essential for cell integrity and fungal virulence in Cryptococcus neoformans.

Authors:  Yina Wang; Tong-Bao Liu; Shyam Patel; Linghuo Jiang; Chaoyang Xue
Journal:  Eukaryot Cell       Date:  2011-09-16

5.  The F-Box protein Fbp1 regulates sexual reproduction and virulence in Cryptococcus neoformans.

Authors:  Tong-Bao Liu; Yina Wang; Sabriya Stukes; Qing Chen; Arturo Casadevall; Chaoyang Xue
Journal:  Eukaryot Cell       Date:  2011-04-08

Review 6.  Hepatocellular carcinoma: Will novel targeted drugs really impact the next future?

Authors:  Liliana Montella; Giovannella Palmieri; Raffaele Addeo; Salvatore Del Prete
Journal:  World J Gastroenterol       Date:  2016-07-21       Impact factor: 5.742

7.  Proteasome inhibition suppresses essential immune functions of human CD4+ T cells.

Authors:  Carsten Berges; Heinrich Haberstock; Dominik Fuchs; Marion Miltz; Mahmoud Sadeghi; Gerhard Opelz; Volker Daniel; Cord Naujokat
Journal:  Immunology       Date:  2008-01-23       Impact factor: 7.397

Review 8.  Growth factor receptors and related signalling pathways as targets for novel treatment strategies of hepatocellular cancer.

Authors:  Michael Höpfner; Detlef Schuppan; Hans Scherübl
Journal:  World J Gastroenterol       Date:  2008-01-07       Impact factor: 5.742

9.  Fbp1-mediated ubiquitin-proteasome pathway controls Cryptococcus neoformans virulence by regulating fungal intracellular growth in macrophages.

Authors:  Tong-Bao Liu; Chaoyang Xue
Journal:  Infect Immun       Date:  2013-11-18       Impact factor: 3.441

10.  Evolving therapies in the treatment of hepatocellular carcinoma.

Authors:  Hans Christian Spangenberg; Robert Thimme; Hubert E Blum
Journal:  Biologics       Date:  2008-09
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