Literature DB >> 2576295

Epidermal growth factor receptors in breast cancer: association with early relapse and death, poor response to hormones and interactions with neu.

A L Harris1, S Nicholson, J R Sainsbury, J Farndon, C Wright.   

Abstract

Epidermal growth factor receptors (EGFRs) were measured in 221 primary breast cancers by ligand binding with 125I-labelled EGF, and high-affinity sites were quantitated. There was a highly significant inverse relationship between oestrogen receptor (ER) and EGFR (15 EGFR-positive [EGFR+]ER+ and 92 EGFR-negative [EGFR-]ER+: 54 EGFR- ER- and 60 EGFR+ ER-). The relapse-free survival and overall survival were significantly shorter for EGFR+ vs EGFR- tumours (P less than 0.001) by about 2 yr in the case of relapse-free survival. When ER- tumours were substratified by EGFR status, the EGFR- ER- tumours had a prognosis almost as good as the ER+ tumours. In 31 of 184 cases, high expression of neu, correlating with amplification, was found. Expression of neu conferred similar poor prognosis to EGFR expression in all prognostic subgroups. Coexpression of neu and EGFR had an additive adverse effect. Epidermal growth factor receptors (EGFR) and oestrogen receptors (ER) were analysed in 221 patients with primary operable breast cancer by means of radioligand assays. After median follow-up of 24 months (range 3-60 months), there had been recurrences in 99 patients, of whom 72 (median age 56 yr, range 32-77 yr) received tamoxifen alone as first-line treatment for recurrence. 14 patients (19%) showed a response to this therapy and 58 (81%) did not. Of 32 ER+ tumours, 12 (37.5%) showed an objective response to tamoxifen compared with only 2 of 40 (5%) ER- tumours (P less than 0.005). Of 35 EGFR+ tumours, 3 (8.5%) achieved an objective response compared with 11 of 36 (30%) EGFR tumours (P less than 0.05). Only 1 of 28 EGFR+, ER- tumours achieved an objective response. Including patients whose disease remained stable for more than 6 months with the responders, however, EGFR status was a better predictor of response to tamoxifen; 15 of 37 EGFR- patients and 5 of 35 EGFR+ patients responded (P less than 0.01).

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Year:  1989        PMID: 2576295     DOI: 10.1016/0022-4731(89)90072-1

Source DB:  PubMed          Journal:  J Steroid Biochem        ISSN: 0022-4731            Impact factor:   4.292


  30 in total

1.  Measurement of occupied and non-occupied epidermal growth factor receptor sites in 216 human breast cancer biopsies.

Authors:  N Falette; M F Lefebvre; F Meggouh; M Eynard; E Garin; S Saez
Journal:  Breast Cancer Res Treat       Date:  1992-03       Impact factor: 4.872

Review 2.  The development, application and limitations of breast cancer cell lines to study tamoxifen and aromatase inhibitor resistance.

Authors:  Cynthie Wong; Shiuan Chen
Journal:  J Steroid Biochem Mol Biol       Date:  2012-01-08       Impact factor: 4.292

3.  Very low prevalence of epidermal growth factor receptor (EGFR) protein expression and gene amplification in Saudi breast cancer patients.

Authors:  Mohamed A Shawarby; Dalal M Al-Tamimi; Ayesha Ahmed
Journal:  Diagn Pathol       Date:  2011-06-24       Impact factor: 2.644

4.  PIK3CA mutations and EGFR overexpression predict for lithium sensitivity in human breast epithelial cells.

Authors:  Michaela J Higgins; Julia A Beaver; Hong Yuen Wong; John P Gustin; Josh D Lauring; Joseph P Garay; Hiroyuki Konishi; Morassa Mohseni; Grace M Wang; Justin Cidado; Danijela Jelovac; David P Cosgrove; Akina Tamaki; Abde M Abukhdeir; Ben Ho Park
Journal:  Cancer Biol Ther       Date:  2011-02-01       Impact factor: 4.742

Review 5.  Therapeutic options for HER-2 positive breast cancer: Perspectives and future directions.

Authors:  Gonzalo Recondo; Enrique Dìaz Canton; Màximo de la Vega; Martin Greco; Gonzalo Recondo; Matias E Valsecchi
Journal:  World J Clin Oncol       Date:  2014-08-10

6.  HER2/NEU GENE EXPRESSION PRODUCTS EVALUATED WITH SUPERPARAMAGNETIC, GENETICALLY ENGINEERED ANTIBODIES.

Authors:  Marek Malecki
Journal:  Proc S Dak Acad Sci       Date:  2007

Review 7.  Present and future evolution of advanced breast cancer therapy.

Authors:  Ricardo H Alvarez
Journal:  Breast Cancer Res       Date:  2010-10-22       Impact factor: 6.466

8.  In vitro and in vivo expressions of transforming growth factor-alpha and tyrosine kinase receptors in human non-small-cell lung carcinomas.

Authors:  C Liu; M S Tsao
Journal:  Am J Pathol       Date:  1993-04       Impact factor: 4.307

9.  p185c-neu and epidermal growth factor receptor associate into a structure composed of activated kinases.

Authors:  X L Quian; S J Decker; M I Greene
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

10.  Tumour markers: An overview.

Authors:  T Malati
Journal:  Indian J Clin Biochem       Date:  2007-09
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