Literature DB >> 8499151

Short recurrence-free survival associated with high oestrogen receptor levels in the natural history of postmenopausal, primary breast cancer.

S M Thorpe1, I J Christensen, B B Rasmussen, C Rose.   

Abstract

The ability of oestrogen and progesterone receptor (ER and PgR, respectively) status to discriminate recurrence-free survival (RFS) among a cohort of consecutively accrued 952 postmenopausal patients has been studied. None of the cohort members investigated were treated with adjuvant therapy. Using a graduated scale of receptor status [low, intermediate and high receptor levels (< 10 vs. 10-107 vs. > or = 108 fmol/mg cytosol protein, respectively)] instead of the more commonly used dichotomous subdivision (positive vs. negative), ER level significantly discriminated between groups of patients with long vs. short RFS. Contrary to our expectations, patients with highest ER levels have as poor a prognosis as ER-negative patients, while patients with intermediate ER levels have longest RFS. The group of patients with ER levels > or = 108 fmol/mg cytosol protein comprises 47% of the cohort. The independent significance of overexpression of ER as a prognostic factor among this patient group is demonstrated in multivariate analysis where ER level is more significant than either grade of anaplasia or tumour size. PgR status did not significantly predict RFS among these patients. While the highest ER levels predispose for poorer prognosis among postmenopausal patients, it is precisely this group that experiences greatest benefit from adjuvant treatment with tamoxifen. Thus, patients who might otherwise go untreated due to their node-negative status can be readily identified and offered adjuvant treatment.

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Year:  1993        PMID: 8499151     DOI: 10.1016/s0959-8049(05)80204-7

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  9 in total

1.  A noncompetitive small molecule inhibitor of estrogen-regulated gene expression and breast cancer cell growth that enhances proteasome-dependent degradation of estrogen receptor {alpha}.

Authors:  Nicole M Kretzer; Milu T Cherian; Chengjian Mao; Irene O Aninye; Philip D Reynolds; Rachel Schiff; Paul J Hergenrother; Steven K Nordeen; Elizabeth M Wilson; David J Shapiro
Journal:  J Biol Chem       Date:  2010-11-01       Impact factor: 5.157

2.  ESR1 gene status correlates with estrogen receptor protein levels measured by ligand binding assay and immunohistochemistry.

Authors:  Anne-Vibeke Laenkholm; Ann Knoop; Bent Ejlertsen; Tine Rudbeck; Maj-Britt Jensen; Sven Müller; Anne Elisabeth Lykkesfeldt; Birgitte Bruun Rasmussen; Kirsten Vang Nielsen
Journal:  Mol Oncol       Date:  2012-05-08       Impact factor: 6.603

3.  Estrogen receptor α inhibitor activates the unfolded protein response, blocks protein synthesis, and induces tumor regression.

Authors:  Neal D Andruska; Xiaobin Zheng; Xujuan Yang; Chengjian Mao; Mathew M Cherian; Lily Mahapatra; William G Helferich; David J Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-30       Impact factor: 11.205

4.  Estrogen receptor quantitative measures and breast cancer survival.

Authors:  Deirdre A Hill; Marc Barry; Charles Wiggins; Andrea Nibbe; Melanie Royce; Eric Prossnitz; Lesley Lomo
Journal:  Breast Cancer Res Treat       Date:  2017-08-19       Impact factor: 4.872

5.  HspBP1 levels are elevated in breast tumor tissue and inversely related to tumor aggressiveness.

Authors:  Ana Paula Souza; Caroline Albuquerque; Carolina Torronteguy; Antonio Frasson; Fabio Maito; Luciana Pereira; Vinícius Duval da Silva; Felipe Zerwes; Deborah Raynes; Vince Guerriero; Cristina Bonorino
Journal:  Cell Stress Chaperones       Date:  2008-11-06       Impact factor: 3.667

6.  A kinetic model identifies phosphorylated estrogen receptor-α (ERα) as a critical regulator of ERα dynamics in breast cancer.

Authors:  Dan Tian; Natalia M Solodin; Prashant Rajbhandari; Kelsi Bjorklund; Elaine T Alarid; Pamela K Kreeger
Journal:  FASEB J       Date:  2015-02-03       Impact factor: 5.191

7.  Overexpression of matrix-metalloproteinase-9 in human breast cancer: a potential favourable indicator in node-negative patients.

Authors:  A Scorilas; A Karameris; N Arnogiannaki; A Ardavanis; P Bassilopoulos; T Trangas; M Talieri
Journal:  Br J Cancer       Date:  2001-06-01       Impact factor: 7.640

8.  Tailoring treatment for ductal intraepithelial neoplasia of the breast according to Ki-67 and molecular phenotype.

Authors:  M Lazzeroni; A Guerrieri-Gonzaga; E Botteri; M C Leonardi; N Rotmensz; D Serrano; C Varricchio; D Disalvatore; A Del Castillo; F Bassi; G Pagani; A DeCensi; G Viale; B Bonanni; G Pruneri
Journal:  Br J Cancer       Date:  2013-04-11       Impact factor: 7.640

9.  Cyclin D1 overexpression is a negative predictive factor for tamoxifen response in postmenopausal breast cancer patients.

Authors:  M Stendahl; A Kronblad; L Rydén; S Emdin; N O Bengtsson; G Landberg
Journal:  Br J Cancer       Date:  2004-05-17       Impact factor: 7.640

  9 in total

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