Literature DB >> 19343299

Targeted therapies in multiple myeloma.

Efstathios Kastritis1, Andreas Charidimou, Andreas Varkaris, Meletios A Dimopoulos.   

Abstract

Increasing knowledge of the biology of multiple myeloma led the way for the development of novel drugs that have changed the management of the disease. New treatments target not only to the malignant plasma cell but also target the interactions of myeloma cells with their microenvironment. Several preclinical studies have identified potential targets and drugs are developed that act on pathways crucial for myeloma cell survival, proliferation, migration and drug resistance. The identification of active agents in the laboratory is followed by rationally designed clinical studies that validate these drugs, either as single agents or in combinations with other active drugs. These novel agents may be either small molecules or monoclonal antibodies targeting receptors, kinase activity of receptors or key molecules within critical pathways, intracellular maintenance mechanisms and immune modulation.

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Year:  2009        PMID: 19343299     DOI: 10.1007/s11523-008-0102-9

Source DB:  PubMed          Journal:  Target Oncol        ISSN: 1776-2596            Impact factor:   4.493


  119 in total

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Journal:  Blood       Date:  2004-01-15       Impact factor: 22.113

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Journal:  Blood       Date:  2002-10-03       Impact factor: 22.113

10.  Heat shock protein inhibition is associated with activation of the unfolded protein response pathway in myeloma plasma cells.

Authors:  Emma L Davenport; Hannah E Moore; Alan S Dunlop; Swee Y Sharp; Paul Workman; Gareth J Morgan; Faith E Davies
Journal:  Blood       Date:  2007-05-24       Impact factor: 22.113

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Review 3.  Novel strategies for immunotherapy in multiple myeloma: previous experience and future directions.

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Review 5.  Tumor-related interleukins: old validated targets for new anti-cancer drug development.

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Journal:  Mol Cancer       Date:  2017-09-19       Impact factor: 27.401

6.  Expression and Polymorphism of Toll-Like Receptor 4 and Effect on NF-κB Mediated Inflammation in Colon Cancer Patients.

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7.  FBXO2 modulates STAT3 signaling to regulate proliferation and tumorigenicity of osteosarcoma cells.

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  7 in total

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