Literature DB >> 27225751

The distribution pattern of ERα expression, ESR1 genetic variation and expression of growth factor receptors: association with breast cancer prognosis in Russian patients treated with adjuvant tamoxifen.

Nataliya Babyshkina1,2, Sergey Vtorushin3,4, Marina Zavyalova3,5,4, Stanislav Patalyak6, Tatyana Dronova7, Nikolay Litviakov7,5, Elena Slonimskaya6,4, Julia Kzhyshkowska5,8, Nadejda Cherdyntseva7,5,4, Evgeny Choynzonov9.   

Abstract

Identification of additional biomarkers associated with ER genomic and nongenomic pathways could be very useful to distinguish patients who will benefit from tamoxifen treatment. The aim of this study was to analyze the prognostic significance of the distribution pattern of ERα expression, ESR1 gene single-nucleotide polymorphisms and expression levels of growth factor receptors in Russian hormone receptor-positive breast cancer patients treated with adjuvant tamoxifen. Formalin-fixed paraffin-embedded tumor tissue samples from 97 patients were examined for the distribution pattern of ERα expression, as well as for EGFR and TGF-βR1 expression by immunohistochemistry. Genotypes for ESR1 +30T>C (rs2077647) and ESR1 2014G>A (rs2228480) were analyzed using a TaqMan assay. Progression-free survival (PFS) was used as an endpoint for the survival analyses. We found that patients with the heterogeneous distribution of ERα expression had poor prognosis on tamoxifen treatment (P = 0.021). We identified a high EGFR expression in patients who developed distant metastasis or recurrence during tamoxifen treatment (a tamoxifen-resistant group-TR) in contrast to the distant metastasis-free patients (a tamoxifen-sensitive group-TS) (80.0 vs. 41.9 %, respectively, P = 0.009). Carriers of the ESR12014A mutant allele were more prevalent among the TR patients compared to the TS patients (26.3 vs. 8.0 %, respectively, P = 0.009). EGFR expression and the distribution pattern of ERα expression were associated with the response to tamoxifen by both univariate and multivariate logistic regression analyses. The presence of these markers either alone or in combination was correlated with the worse PFS for all patients. Analysis of the distribution pattern of ERα expression and the EGFR status in tumor tissue may be valuable for patient selection for tamoxifen adjuvant therapy.

Entities:  

Keywords:  Breast cancer; EGFR expression; ERα expression; Prognosis markers; Single-nucleotide polymorphisms; Tamoxifen resistance

Mesh:

Substances:

Year:  2016        PMID: 27225751     DOI: 10.1007/s10238-016-0428-z

Source DB:  PubMed          Journal:  Clin Exp Med        ISSN: 1591-8890            Impact factor:   3.984


  34 in total

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Authors:  Marina V Zavyalova; Evgeny V Denisov; Lubov A Tashireva; Tatiana S Gerashchenko; Nikolay V Litviakov; Nikolay A Skryabin; Sergey V Vtorushin; Nadezhda S Telegina; Elena M Slonimskaya; Nadezhda V Cherdyntseva; Vladimir M Perelmuter
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  3 in total

1.  Impact of estrogen receptor α on the tamoxifen response and prognosis in luminal-A-like and luminal-B-like breast cancer.

Authors:  Nataliya Babyshkina; Sergey Vtorushin; Tatyana Dronova; Stanislav Patalyak; Elena Slonimskaya; Julia Kzhyshkowska; Nadejda Cherdyntseva; Evgeny Choynzonov
Journal:  Clin Exp Med       Date:  2019-09-27       Impact factor: 3.984

2.  Predictive value of vascular endothelial growth factor receptor type 2 in triple-negative breast cancer patients treated with neoadjuvant chemotherapy.

Authors:  Nataliya Babyshkina; Marina Zavyalova; Natalia Tarabanovskaya; Tatyana Dronova; Nadejda Krakhmal; Elena Slonimskaya; Julia Kzhyshkowska; Evgeny Choynzonov; Nadejda Cherdyntseva
Journal:  Mol Cell Biochem       Date:  2017-12-11       Impact factor: 3.396

3.  Molecular markers associated with the outcome of tamoxifen treatment in estrogen receptor-positive breast cancer patients: scoping review and in silico analysis.

Authors:  Maiquidieli Dal Berto; Giovana Tavares Dos Santos; Aniúsca Vieira Dos Santos; Andrew Oliveira Silva; José Eduardo Vargas; Rafael José Vargas Alves; Fernanda Barbisan; Ivana Beatrice Mânica da Cruz; Claudia Giuliano Bica
Journal:  Discov Oncol       Date:  2021-10-01
  3 in total

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