Literature DB >> 11129170

ZD1839 ('Iressa') as an anticancer agent.

J Baselga1, S D Averbuch.   

Abstract

ZD1839 ('Iressa') is an orally active, selective epidermal growth factor receptor-tyrosine kinase inhibitor which blocks signal transduction pathways implicated in the proliferation and survival of cancer cells and other host-dependent processes promoting cancer growth. In preclinical studies, ZD1839 produced reversible growth inhibition and growth delay in a wide range of tumour cell lines and human tumour xenografts. Moreover, this activity was enhanced when ZD1839 was coadministered with cytotoxic agents. Preliminary results from phase I trials in patients with advanced disease and a wide variety of tumour types suggest that ZD1839 has an acceptable tolerability profile and promising clinical efficacy, particularly in non-small cell lung cancer (NSCLC). ZD1839 is currently in phase III clinical development for the treatment of advanced NSCLC. In addition, further trials are ongoing or planned in a number of other tumour types.

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Year:  2000        PMID: 11129170     DOI: 10.2165/00003495-200060001-00004

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  15 in total

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Review 2.  The role of polypeptide growth factors in human carcinomas: new targets for a novel pharmacological approach.

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Journal:  Pharmacol Rev       Date:  2000-06       Impact factor: 25.468

Review 3.  Tyrosine kinases and their interactions with signalling proteins.

Authors:  T Pawson
Journal:  Curr Opin Genet Dev       Date:  1992-02       Impact factor: 5.578

Review 4.  Evolution of cisplatin-based chemotherapy in non-small cell lung cancer: a historical perspective and the eastern cooperative oncology group experience.

Authors:  D H Johnson
Journal:  Chest       Date:  2000-04       Impact factor: 9.410

5.  Receptor dimerization is not a factor in the signalling activity of a transforming variant epidermal growth factor receptor (EGFRvIII).

Authors:  C T Chu; K D Everiss; C J Wikstrand; S K Batra; H J Kung; D D Bigner
Journal:  Biochem J       Date:  1997-06-15       Impact factor: 3.857

Review 6.  Regulation of signal transduction and signal diversity by receptor oligomerization.

Authors:  M A Lemmon; J Schlessinger
Journal:  Trends Biochem Sci       Date:  1994-11       Impact factor: 13.807

7.  Antitumor effect and potentiation of cytotoxic drugs activity in human cancer cells by ZD-1839 (Iressa), an epidermal growth factor receptor-selective tyrosine kinase inhibitor.

Authors:  F Ciardiello; R Caputo; R Bianco; V Damiano; G Pomatico; S De Placido; A R Bianco; G Tortora
Journal:  Clin Cancer Res       Date:  2000-05       Impact factor: 12.531

8.  ErbB2 potentiates breast tumor proliferation through modulation of p27(Kip1)-Cdk2 complex formation: receptor overexpression does not determine growth dependency.

Authors:  H A Lane; I Beuvink; A B Motoyama; J M Daly; R M Neve; N E Hynes
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

9.  Epidermal growth factor ligand-independent, unregulated, cell-transforming potential of a naturally occurring human mutant EGFRvIII gene.

Authors:  S K Batra; S Castelino-Prabhu; C J Wikstrand; X Zhu; P A Humphrey; H S Friedman; D D Bigner
Journal:  Cell Growth Differ       Date:  1995-10

Review 10.  Chemotherapy for non-small cell lung cancer: have we reached a new plateau?

Authors:  F A Shepherd
Journal:  Semin Oncol       Date:  1999-02       Impact factor: 4.929

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  47 in total

Review 1.  Drug Resistance to EGFR Inhibitors in Lung Cancer.

Authors:  Osamu Tetsu; Matthew J Hangauer; Janyaporn Phuchareon; David W Eisele; Frank McCormick
Journal:  Chemotherapy       Date:  2016-02-25       Impact factor: 2.544

2.  Inhibition of proliferation, migration, and matrix metalloprotease production in malignant mesothelioma cells by tyrosine kinase inhibitors.

Authors:  Zhiwen Liu; Julius Klominek
Journal:  Neoplasia       Date:  2004 Nov-Dec       Impact factor: 5.715

3.  Resolving the EGF-EGFR interaction characteristics through a multiple-temperature, multiple-inhibitor, real-time interaction analysis approach.

Authors:  Hanna Björkelund; Lars Gedda; Magnus Malmqvist; Karl Andersson
Journal:  Mol Clin Oncol       Date:  2012-10-30

Review 4.  Gefitinib: a review of its use in the management of advanced non-small-cell lung cancer.

Authors:  James E Frampton; Stephanie E Easthope
Journal:  Drugs       Date:  2004       Impact factor: 9.546

5.  Tamoxifen resistance in breast cancer cells is accompanied by an enhanced motile and invasive phenotype: inhibition by gefitinib ('Iressa', ZD1839).

Authors:  Stephen Hiscox; Liam Morgan; Denise Barrow; Carol Dutkowskil; Alan Wakeling; Robert I Nicholson
Journal:  Clin Exp Metastasis       Date:  2004       Impact factor: 5.150

6.  Identifying drug effects via pathway alterations using an integer linear programming optimization formulation on phosphoproteomic data.

Authors:  Alexander Mitsos; Ioannis N Melas; Paraskeuas Siminelakis; Aikaterini D Chairakaki; Julio Saez-Rodriguez; Leonidas G Alexopoulos
Journal:  PLoS Comput Biol       Date:  2009-12-04       Impact factor: 4.475

7.  Targeted treatment of advanced and metastaticbreast cancer with lapatinib.

Authors:  Brendan Corkery; Norma O'Donovan; John Crown
Journal:  Onco Targets Ther       Date:  2008-09-01       Impact factor: 4.147

8.  ERBB1 and ERBB2 have distinct functions in tumor cell invasion and intravasation.

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Journal:  Clin Cancer Res       Date:  2009-05-19       Impact factor: 12.531

Review 9.  Imaging of EGFR and EGFR tyrosine kinase overexpression in tumors by nuclear medicine modalities.

Authors:  Eyal Mishani; Galith Abourbeh; Martin Eiblmaier; Carolyn J Anderson
Journal:  Curr Pharm Des       Date:  2008       Impact factor: 3.116

10.  Global effects of kinase inhibitors on signaling networks revealed by quantitative phosphoproteomics.

Authors:  Cuiping Pan; Jesper V Olsen; Henrik Daub; Matthias Mann
Journal:  Mol Cell Proteomics       Date:  2009-08-03       Impact factor: 5.911

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