Literature DB >> 19733440

Irreversible pan-ErbB tyrosine kinase inhibitors and breast cancer: current status and future directions.

Alberto Ocaña1, Eitan Amir.   

Abstract

Aberrant activation of HER2 through overexpression has been shown to play an important role in some breast cancers. Therapies against this receptor including the monoclonal antibody, trastuzumab, or the small tyrosine kinase inhibitor, lapatinib have shown to improve the prognosis of such patients. Despite overexpressing HER2, some patients do not respond to these targeted treatments or progress after a short period of time. Irreversible tyrosine kinase inhibitors have been developed to bypass several pathways that could be involved in this resistance. In vitro, these agents have been shown to be more potent and to prolong target inhibition. Clinical development of these agents is ongoing and early results are promising. This review will describe the biologic rationale that justifies the development of these agents in breast cancer focusing on the current status and future directions.

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Year:  2009        PMID: 19733440     DOI: 10.1016/j.ctrv.2009.08.001

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


  15 in total

Review 1.  Preclinical development of molecular-targeted agents for cancer.

Authors:  Alberto Ocana; Atanasio Pandiella; Lillian L Siu; Ian F Tannock
Journal:  Nat Rev Clin Oncol       Date:  2010-12-07       Impact factor: 66.675

2.  Reversible, allosteric small-molecule inhibitors of regulator of G protein signaling proteins.

Authors:  Levi L Blazer; David L Roman; Alfred Chung; Martha J Larsen; Benjamin M Greedy; Stephen M Husbands; Richard R Neubig
Journal:  Mol Pharmacol       Date:  2010-06-22       Impact factor: 4.436

3.  Targeting the human epidermal growth factor receptor 2 pathway in breast cancer.

Authors:  Senthilkumar Damodaran; Erin M Olson
Journal:  Hosp Pract (1995)       Date:  2012-10

Review 4.  Treatment of HER2-positive breast cancer: current status and future perspectives.

Authors:  Carlos L Arteaga; Mark X Sliwkowski; C Kent Osborne; Edith A Perez; Fabio Puglisi; Luca Gianni
Journal:  Nat Rev Clin Oncol       Date:  2011-11-29       Impact factor: 66.675

5.  A growing family: adding mutated Erbb4 as a novel cancer target.

Authors:  Udo Rudloff; Yardena Samuels
Journal:  Cell Cycle       Date:  2010-04-15       Impact factor: 4.534

6.  A nanomolar-potency small molecule inhibitor of regulator of G-protein signaling proteins.

Authors:  Levi L Blazer; Haoming Zhang; Emma M Casey; Stephen M Husbands; Richard R Neubig
Journal:  Biochemistry       Date:  2011-03-29       Impact factor: 3.162

Review 7.  Personalized therapies in the cancer "omics" era.

Authors:  Alberto Ocaña; Atanasio Pandiella
Journal:  Mol Cancer       Date:  2010-07-29       Impact factor: 27.401

Review 8.  Potential of afatinib in the treatment of patients with HER2-positive breast cancer.

Authors:  Elena Geuna; Filippo Montemurro; Massimo Aglietta; Giorgio Valabrega
Journal:  Breast Cancer (Dove Med Press)       Date:  2012-08-27

9.  A fluorescent reporter of ATP binding-competent receptor kinases.

Authors:  Renaud Sicard; Jyothi Dhuguru; Wenjun Liu; Nirav Patel; Ralf Landgraf; James N Wilson
Journal:  Bioorg Med Chem Lett       Date:  2012-07-20       Impact factor: 2.823

10.  Human breast cancer cells harboring a gatekeeper T798M mutation in HER2 overexpress EGFR ligands and are sensitive to dual inhibition of EGFR and HER2.

Authors:  Brent N Rexer; Ritwik Ghosh; Archana Narasanna; Mónica Valeria Estrada; Anindita Chakrabarty; Youngchul Song; Jeffrey A Engelman; Carlos L Arteaga
Journal:  Clin Cancer Res       Date:  2013-08-15       Impact factor: 12.531

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