Literature DB >> 17826917

Molecular-targeted therapies: lessons from years of clinical development.

Daniela D Rosa1, Gustavo Ismael, Lissandra Dal Lago, Ahmad Awada.   

Abstract

Over the past decade, molecular-targeted therapies have been added to cytotoxic and anti-endocrine drugs in the treatment of cancer, with the aim to target the molecular pathways that underlie the carcinogenic process and maintain the cancer phenotype. Success with some of these agents has suggested that identification and validation of the drug target is the starting point for the route of development of active, safe and effective drugs. Main molecular targets used to the development of anticancer drugs are cell surface receptors, signal transduction pathways, gene transcription targets, ubiquitin-proteasome/heat shock proteins and tumour microenvironment components (especially antiangiogenic agents). Here, we review the development of the main molecular targeted non-cytotoxic agents studied in cancer, highlighting lessons derived from the development of these novel drugs and proposing new horizons for the clinical development of molecular-targeted therapies.

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Year:  2007        PMID: 17826917     DOI: 10.1016/j.ctrv.2007.07.019

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  15 in total

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Review 5.  Novel therapies against aggressive and recurrent epithelial cancers by molecular targeting tumor- and metastasis-initiating cells and their progenies.

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Review 6.  The path to clinical proteomics research: integration of proteomics, genomics, clinical laboratory and regulatory science.

Authors:  Emily S Boja; Henry Rodriguez
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Review 8.  Recent advances relating to the clinical application of naked monoclonal antibodies in solid tumors.

Authors:  Andreas A Argyriou; Haralabos P Kalofonos
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9.  Clinical proteomics and OMICS clues useful in translational medicine research.

Authors:  Elena López; Luis Madero; Juan López-Pascual; Martin Latterich
Journal:  Proteome Sci       Date:  2012-05-29       Impact factor: 2.480

10.  High susceptibility of metastatic cells derived from human prostate and colon cancer cells to TRAIL and sensitization of TRAIL-insensitive primary cells to TRAIL by 4,5-dimethoxy-2-nitrobenzaldehyde.

Authors:  Hak-Bong Kim; Mi-Ju Kim; Dae-Young Kim; Jae-Won Lee; Jae-Ho Bae; Dong-Wan Kim; Chi-Dug Kang; Sun-Hee Kim
Journal:  Mol Cancer       Date:  2011-04-25       Impact factor: 27.401

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