Literature DB >> 12750551

Why Iressa failed: toward novel use of kinase inhibitors (outlook).

Mikhail V Blagosklonny1, Zbigniew Darzynkiewicz.   

Abstract

A phase III failure of Iressa, an inhibitor of the EGF receptor (EGFR), is viewed as a surprise. With a few exceptions, however, inhibitors of EGFR cannot be effective as a monotherapy in cancers with additional oncogenic changes (downstream of EGFR), which cause mitogen-independent proliferation. In other cases, combining these inhibitors with chemotherapy may lead to antagonism in cancer cells and/or aggravated side-effects. This review discusses why neither levels of EGFR nor doses of Iressa correlate with clinical response. We suggest a novel use of signal transduction inhibitors, including Iressa, to increase therapeutic index by modulating cycle-dependent and apoptosis-inducing chemotherapies. This approach may be most beneficial to patients who do not respond to monotherapy with kinase inhibitors. Development of molecular diagnostics will further diversify these strategies.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12750551     DOI: 10.4161/cbt.2.2.286

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


  6 in total

1.  Lipid raft localization of EGFR alters the response of cancer cells to the EGFR tyrosine kinase inhibitor gefitinib.

Authors:  Mary E Irwin; Kelly L Mueller; Natacha Bohin; Yubin Ge; Julie L Boerner
Journal:  J Cell Physiol       Date:  2011-09       Impact factor: 6.384

2.  Met and c-Src cooperate to compensate for loss of epidermal growth factor receptor kinase activity in breast cancer cells.

Authors:  Kelly L Mueller; Lauren A Hunter; Stephen P Ethier; Julie L Boerner
Journal:  Cancer Res       Date:  2008-05-01       Impact factor: 12.701

Review 3.  Cellular responses to EGFR inhibitors and their relevance to cancer therapy.

Authors:  Pinaki R Dutta; Amit Maity
Journal:  Cancer Lett       Date:  2007-03-23       Impact factor: 8.679

4.  A multiple reaction monitoring (MRM) method to detect Bcr-Abl kinase activity in CML using a peptide biosensor.

Authors:  Tzu-Yi Yang; Christie L Eissler; Mark C Hall; Laurie L Parker
Journal:  PLoS One       Date:  2013-02-20       Impact factor: 3.240

5.  Novel strategies of protecting non-cancer cells during chemotherapy: are they ready for clinical testing?

Authors:  Zbigniew Darzynkiewicz
Journal:  Oncotarget       Date:  2011-03

6.  Transphosphorylation of kinase-dead HER3 and breast cancer progression: a new standpoint or an old concept revisited?

Authors:  Javier A Menendez; Ruth Lupu
Journal:  Breast Cancer Res       Date:  2007       Impact factor: 6.466

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.