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Table of Contents
Vol. 68, No. 4-6, 2005
Issue release date: August 2005
Section title: Laboratory Investigation
Oncology 2005;68:538–547
(DOI:10.1159/000086998)

Inhibitors of Epidermoid Growth Factor Receptor Suppress Cell Growth and Enhance Chemosensitivity of Nasopharyngeal Cancer Cells in vitro

Hsu C.-H.a,e · Gao M.a,e · Chen C.-L.b,d · Yeh P.-Y.a,e · Cheng A.-L.a,c,e
Departments of aOncology, bPathology and cInternal Medicine, National Taiwan University Hospital, dDepartment of Pathology, Wanfang Hospital and Taipei Medical University, and eCancer Research Center, National Taiwan University College of Medicine, Taipei, Taiwan

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Article / Publication Details

First-Page Preview
Abstract of Laboratory Investigation

Received: August 12, 2004
Accepted: November 14, 2004
Published online: August 17, 2005
Issue release date: August 2005

Number of Print Pages: 10
Number of Figures: 7
Number of Tables: 0

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: http://www.karger.com/OCL

Abstract

Objective: Epidermoid growth factor receptor (EGFR, HER1) is overexpressed in a majority of head-and-neck cancers, including nasopharyngeal carcinoma (NPC). Although EGFR inhibitors appear to be effective for some head-and-neck cancers, their efficacy in NPC remains unclear. Methods: The effect of EGFR-specific tyrosine kinase inhibitors, including PD153035 and ZD1839, were studied in NPC-TW01, NPC-TW04, and HONE1 cell lines. The effect of combining EGFR inhibitors with cytotoxic agents was evaluated in NPC-TW04 cells. Results: All three NPC cell lines expressed EGFR. PD153035 and ZD1839 inhibited the growth of NPC cells with IC50s around 10 and 20 µM, respectively. These inhibitors, however, effectively suppressed ligand-stimulated EGFR activation in NPC cells with a much lower concentration (≧0.1 µM). The growth-suppression activity of EGFR inhibitors was closely associated with suppression of AKT phosphorylation. LY294002, a phosphatidylinositol-3 kinase (P13K)/AKT inhibitor, did suppress the growth of NPC cells. Pretreatment of EGFR inhibitors by 24 h significantly enhanced the cytotoxic effect of doxorubicin, paclitaxel, cisplatin, and 5-fluororuacil in NPC-TW04 cells. Conclusions: Our data indicate that inhibition of EGFR activation is not sufficient to induce growth inhibition in NPC cells in vitro. EGFR inhibitors may be useful adjuncts in treating NPC when combined with conventional anticancer drugs.

© 2005 S. Karger AG, Basel


Article / Publication Details

First-Page Preview
Abstract of Laboratory Investigation

Received: August 12, 2004
Accepted: November 14, 2004
Published online: August 17, 2005
Issue release date: August 2005

Number of Print Pages: 10
Number of Figures: 7
Number of Tables: 0

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: http://www.karger.com/OCL


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