Literature DB >> 27810901

High Estrogen Receptor β Expression Is Prognostic among Adjuvant Chemotherapy-Treated Patients-Results from a Population-Based Breast Cancer Cohort.

Karin Elebro1,2, Signe Borgquist1,3, Ann H Rosendahl1, Andrea Markkula1, Maria Simonsson1, Karin Jirström1, Carsten Rose4, Christian Ingvar5, Helena Jernström6.   

Abstract

PURPOSE: Isoform-specific tumor estrogen receptor β (ERβ) expression may hold prognostic information in breast cancer, especially among endocrine-treated breast cancer patients. The study's purpose was to evaluate ERβ isoform 1 (ERβ1) expression in relation to tumor characteristics, ESR2 genotypes, and prognosis in different treatment groups. EXPERIMENTAL
DESIGN: A population-based prospective cohort of 1,026 patients diagnosed with primary invasive breast cancer in Lund, Sweden, between October 2002 and June 2012 was followed until June 2014 (median 5 years). Associations between immunohistochemical ERβ1 expression, patient and tumor characteristics, as well as outcome within treatment groups were analyzed.
RESULTS: Tumor ERβ1 expression was available for 911 patients (89%) and was not associated with ESR2 genotypes. ERβ1 positivity, defined as >75% (ERβ175+, 72.7%), was positively associated with established favorable tumor characteristics. Overall, ERβ175+ was associated with lower risk of breast cancer events [HRadj = 0.60; 95% confidence interval (CI), 0.41-0.89]. The magnitude of the association was larger in patients with ERα- tumors (HRadj = 0.30; 95% CI, 0.12-0.76), compared with ERα+ tumors (HRadj = 0.66; 95% CI, 0.42-1.03). Among the 232 chemotherapy-treated patients, ERβ175+ tumors were associated with lower risk of breast cancer events compared with ERβ175- tumors (HRadj = 0.31; 95% CI, 0.15-0.64). Among the 671 chemonaïve patients, ERβ175 status was not associated with the outcome.
CONCLUSIONS: High ERβ1 expression was a favorable prognostic marker in this breast cancer cohort, especially in chemotherapy-treated patients, but not in endocrine therapy-treated patients. These results warrant confirmation, preferably via a biomarker study in a previously conducted randomized trial. Clin Cancer Res; 23(3); 766-77. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27810901     DOI: 10.1158/1078-0432.CCR-16-1095

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  10 in total

1.  ERβ Isoforms Have Differential Clinical Significance in Breast Cancer Subtypes and Subgroups.

Authors:  Young Choi; Hadong Kim; Simcha Pollack
Journal:  Curr Issues Mol Biol       Date:  2022-04-06       Impact factor: 2.976

2.  RNA-Seq of Circulating Tumor Cells in Stage II-III Breast Cancer.

Authors:  Julie E Lang; Alexander Ring; Tania Porras; Pushpinder Kaur; Victoria A Forte; Neal Mineyev; Debu Tripathy; Michael F Press; Daniel Campo
Journal:  Ann Surg Oncol       Date:  2018-06-04       Impact factor: 5.344

3.  ERβ modulates genistein's cisplatin-enhancing activities in breast cancer MDA-MB-231 cells via P53-independent pathway.

Authors:  Ren Liu; Xiaolin Xu; Chenglin Liang; Xin Chen; Xiaowei Yu; Hongfei Zhong; Wenxiu Xu; Yu Cheng; Wei Wang; Yudong Wu; Lehan Yu; Xiaojuan Hu
Journal:  Mol Cell Biochem       Date:  2019-02-08       Impact factor: 3.396

4.  Insufficient antibody validation challenges oestrogen receptor beta research.

Authors:  Sandra Andersson; Mårten Sundberg; Nusa Pristovsek; Ahmed Ibrahim; Philip Jonsson; Borbala Katona; Carl-Magnus Clausson; Agata Zieba; Margareta Ramström; Ola Söderberg; Cecilia Williams; Anna Asplund
Journal:  Nat Commun       Date:  2017-06-15       Impact factor: 14.919

5.  ERβ alters the chemosensitivity of luminal breast cancer cells by regulating p53 function.

Authors:  Igor Bado; Eric Pham; Benjamin Soibam; Fotis Nikolos; Jan-Åke Gustafsson; Christoforos Thomas
Journal:  Oncotarget       Date:  2018-04-27

6.  Immune gene expression profiling reveals heterogeneity in luminal breast tumors.

Authors:  Bin Zhu; Lap Ah Tse; Difei Wang; Hela Koka; Tongwu Zhang; Mustapha Abubakar; Priscilla Lee; Feng Wang; Cherry Wu; Koon Ho Tsang; Wing-Cheong Chan; Sze Hong Law; Mengjie Li; Wentao Li; Suyang Wu; Zhiguang Liu; Bixia Huang; Han Zhang; Eric Tang; Zhengyan Kan; Soohyeon Lee; Yeon Hee Park; Seok Jin Nam; Mingyi Wang; Xuezheng Sun; Kristine Jones; Bin Zhu; Amy Hutchinson; Belynda Hicks; Ludmila Prokunina-Olsson; Jianxin Shi; Montserrat Garcia-Closas; Stephen Chanock; Xiaohong R Yang
Journal:  Breast Cancer Res       Date:  2019-12-19       Impact factor: 6.466

Review 7.  The role of estrogen receptor beta in breast cancer.

Authors:  Yujing Zhou; Xingdang Liu
Journal:  Biomark Res       Date:  2020-09-07

8.  Clinical associations of ESR2 (estrogen receptor beta) expression across thousands of primary breast tumors.

Authors:  Hina Dalal; Malin Dahlgren; Sergii Gladchuk; Christian Brueffer; Sofia K Gruvberger-Saal; Lao H Saal
Journal:  Sci Rep       Date:  2022-03-18       Impact factor: 4.379

Review 9.  Estrogen Receptor β Expression and Its Clinical Implication in Breast Cancers: Favorable or Unfavorable?

Authors:  Young Choi
Journal:  J Breast Cancer       Date:  2022-02-21       Impact factor: 2.922

10.  Tamoxifen induces hypercoagulation and alterations in ERα and ERβ dependent on breast cancer sub-phenotype ex vivo.

Authors:  K Pather; T N Augustine
Journal:  Sci Rep       Date:  2020-11-06       Impact factor: 4.379

  10 in total

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