Literature DB >> 18072233

Predicting response and resistance to endocrine therapy: profiling patients on aromatase inhibitors.

William R Miller1, Alexey Larionov1, Thomas J Anderson1, John R Walker2, Andreas Krause3, Dean B Evans3, J Michael Dixon1.   

Abstract

Selection for endocrine therapy requires the identification of markers that accurately predict response/resistance. In this report, the authors review their published work and abstract results from an unpublished study to illustrate the potential of RNA microarrays from sequential tumor biopsies from patients who were offered neoadjuvant endocrine therapy treatment to identify the molecular signatures associated with tumor sensitivity/resistance. Clinical response was assessed by serial ultrasound measurements in postmenopausal women with large, primary, estrogen receptor-rich breast cancers who received neoadjuvant treatment with letrozole for 3 months. Tumor RNA from biopsies that were taken before and after 14 days of treatment was hybridized on Affymetrix U133A chips to determine expression profiles. Classic estrogen-dependent genes and markers of proliferation were changed with treatment in most tumors but were poorly associated with clinical response (they frequently were changed in letrozole-resistant tumors). Differential expression patterns could be used to identify heterogeneity in clinically resistant tumors. The results indicated that molecular profiling of early changes with letrozole treatment offers the opportunity to distinguish between clinically responsive and nonresponsive tumors and provides important information about the heterogeneity of endocrine resistance. Cancer 2008. (c) 2007 American Cancer Society.

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Year:  2008        PMID: 18072233     DOI: 10.1002/cncr.23187

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  6 in total

1.  BASP1 interacts with oestrogen receptor α and modifies the tamoxifen response.

Authors:  Lindsey A Marsh; Samantha Carrera; Jayasha Shandilya; Kate J Heesom; Andrew D Davidson; Kathryn F Medler; Stefan Ge Roberts
Journal:  Cell Death Dis       Date:  2017-05-11       Impact factor: 8.469

2.  In situ aromatase expression in primary tumor is associated with estrogen receptor expression but is not predictive of response to endocrine therapy in advanced breast cancer.

Authors:  Anne E Lykkesfeldt; Katrine L Henriksen; Birgitte B Rasmussen; Hironobu Sasano; Dean B Evans; Susanne Møller; Bent Ejlertsen; Henning T Mouridsen
Journal:  BMC Cancer       Date:  2009-06-16       Impact factor: 4.430

3.  Approaches towards expression profiling the response to treatment.

Authors:  Andrew H Sims; John M S Bartlett
Journal:  Breast Cancer Res       Date:  2008-12-08       Impact factor: 6.466

4.  An updated review on the efficacy of adjuvant endocrine therapies in hormone receptor-positive early breast cancer.

Authors:  S Verma; S Sehdev; A Joy; Y Madarnas; J Younus; J A Roy
Journal:  Curr Oncol       Date:  2009-07       Impact factor: 3.677

5.  Identification and mechanisms of endocrine resistance.

Authors:  William R Miller
Journal:  Breast Cancer Res       Date:  2008-12-18       Impact factor: 6.466

6.  Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers.

Authors:  Christopher A Miller; Yevgeniy Gindin; Charles Lu; Obi L Griffith; Malachi Griffith; Dong Shen; Jeremy Hoog; Tiandao Li; David E Larson; Mark Watson; Sherri R Davies; Kelly Hunt; Vera J Suman; Jacqueline Snider; Thomas Walsh; Graham A Colditz; Katherine DeSchryver; Richard K Wilson; Elaine R Mardis; Matthew J Ellis
Journal:  Nat Commun       Date:  2016-08-09       Impact factor: 14.919

  6 in total

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