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PMID: 15324690 Published · ppublish English Journal Article Comment

Successful targeting of ErbB2 receptors-is PTEN the key?

Cancer cell ·Vol. 6 ·No. 2 ·2004-08-00 ·Pages 103-4

Crowder RJ, Lombardi DP, Ellis MJ

Abstract

Women with ErbB2-positive breast cancer have a poor prognosis, and frequently, chemotherapy treatment is ineffective. The ErbB2-targeted antibody trastuzumab improves survival when given with chemotherapy to patients with ErbB2-overexpressing metastatic disease, but treatment is not curative, and primary resistance is common. Postulated mechanisms of action for trastuzumab include immune-mediated cytotoxicity and receptor downmodulation. A study in this issue of Cancer Cell suggests that trastuzumab causes rapid activation of the PTEN lipid phosphatase, which in turn downregulates the phosphatidylinositol 3'-kinase (PI3K) pathway. Resistance to trastuzumab occurs when PTEN function is lost, suggesting that PTEN activation is a critical component of the therapeutic effect.

MeSH Terms
Antibodies, Monoclonal/metabolism,therapeutic use Antibodies, Monoclonal, Humanized Antineoplastic Agents/metabolism,therapeutic use Breast Neoplasms/diagnosis,drug therapy,metabolism Enzyme Activation Female Genes, Tumor Suppressor Humans PTEN Phosphohydrolase Phosphatidylinositol 3-Kinases/metabolism Phosphoric Monoester Hydrolases/metabolism Receptor, ErbB-2/metabolism Signal Transduction/physiology Trastuzumab Tumor Suppressor Proteins/metabolism
Chemicals
Antibodies, Monoclonal Antibodies, Monoclonal, Humanized Antineoplastic Agents Tumor Suppressor Proteins Phosphatidylinositol 3-Kinases Receptor, ErbB-2 Phosphoric Monoester Hydrolases PTEN Phosphohydrolase PTEN protein, human Trastuzumab
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Crowder Robert J
Department of Medicine, Division of Oncology, Washington University School of Medicine and Siteman Cancer Center, Campus Box 8056, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Lombardi Donald P
Ellis Matthew J
Article Info
Journal
Cancer cell
Abbr.
Cancer Cell
ISSN
1535-6108
Published
2004-08-00
Pages
103-4
Language
English
Region
United States
NLM ID
101130617
Subset
IM
Corrections
CommentOn
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