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pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer

Estradiol is a key factor for tumorigenesis and prognosis of hormone receptor-positive breast cancer. Adipocytes are one source of estradiol in patients with breast cancer. Recent studies have shown that phosphorylated ribosomal protein S6 kinase-1 plays a critical role in adipogenesis. Therefore, e...

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Autores principales: Park, Chan Sub, Choi, Jihye, Seong, Min-Ki, Hong, Sung-Eun, Kim, Jae-Sung, Park, In-Chul, Seol, Hyesil, Noh, Woo Chul, Kim, Hyun-Ah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599072/
https://www.ncbi.nlm.nih.gov/pubmed/31252399
http://dx.doi.org/10.1530/EC-19-0101
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author Park, Chan Sub
Choi, Jihye
Seong, Min-Ki
Hong, Sung-Eun
Kim, Jae-Sung
Park, In-Chul
Seol, Hyesil
Noh, Woo Chul
Kim, Hyun-Ah
author_facet Park, Chan Sub
Choi, Jihye
Seong, Min-Ki
Hong, Sung-Eun
Kim, Jae-Sung
Park, In-Chul
Seol, Hyesil
Noh, Woo Chul
Kim, Hyun-Ah
author_sort Park, Chan Sub
collection PubMed
description Estradiol is a key factor for tumorigenesis and prognosis of hormone receptor-positive breast cancer. Adipocytes are one source of estradiol in patients with breast cancer. Recent studies have shown that phosphorylated ribosomal protein S6 kinase-1 plays a critical role in adipogenesis. Therefore, estrogen depletion therapy might have beneficial effects in phosphorylated ribosomal protein S6 kinase-1-positive breast cancer. This study was conducted to evaluate the value of phosphorylated ribosomal protein S6 kinase-1 as a marker for gonadotropin-releasing hormone agonist treatment, a form of estrogen depletion therapy, for premenopausal patients with HR-positive, human epidermal growth factor receptor 2-negative breast cancer. We reviewed the medical records of 296 premenopausal patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative primary invasive breast cancer treated between 2008 and 2015. Phosphorylated ribosomal protein S6 kinase-1 positivity was defined by immunohistochemical staining scores of 1+, 2+ and 3+, whereas a score of 0 was considered negative. Phosphorylated ribosomal protein S6 kinase-1-positive tumors were found in 74.0% of the patients. In the phosphorylated ribosomal protein S6 kinase-1-positive group, disease-free survival of patients treated with a gonadotropin-releasing hormone agonist was significantly longer than that of patients treated without a gonadotropin-releasing hormone agonist (mean 106.7 months vs mean 91.1 months, P = 0.018). Phosphorylated ribosomal protein S6 kinase-1 is a potential biomarker for predicting the efficacy of gonadotropin-releasing hormone agonist therapy in premenopausal patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer.
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spelling pubmed-65990722019-07-03 pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer Park, Chan Sub Choi, Jihye Seong, Min-Ki Hong, Sung-Eun Kim, Jae-Sung Park, In-Chul Seol, Hyesil Noh, Woo Chul Kim, Hyun-Ah Endocr Connect Research Estradiol is a key factor for tumorigenesis and prognosis of hormone receptor-positive breast cancer. Adipocytes are one source of estradiol in patients with breast cancer. Recent studies have shown that phosphorylated ribosomal protein S6 kinase-1 plays a critical role in adipogenesis. Therefore, estrogen depletion therapy might have beneficial effects in phosphorylated ribosomal protein S6 kinase-1-positive breast cancer. This study was conducted to evaluate the value of phosphorylated ribosomal protein S6 kinase-1 as a marker for gonadotropin-releasing hormone agonist treatment, a form of estrogen depletion therapy, for premenopausal patients with HR-positive, human epidermal growth factor receptor 2-negative breast cancer. We reviewed the medical records of 296 premenopausal patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative primary invasive breast cancer treated between 2008 and 2015. Phosphorylated ribosomal protein S6 kinase-1 positivity was defined by immunohistochemical staining scores of 1+, 2+ and 3+, whereas a score of 0 was considered negative. Phosphorylated ribosomal protein S6 kinase-1-positive tumors were found in 74.0% of the patients. In the phosphorylated ribosomal protein S6 kinase-1-positive group, disease-free survival of patients treated with a gonadotropin-releasing hormone agonist was significantly longer than that of patients treated without a gonadotropin-releasing hormone agonist (mean 106.7 months vs mean 91.1 months, P = 0.018). Phosphorylated ribosomal protein S6 kinase-1 is a potential biomarker for predicting the efficacy of gonadotropin-releasing hormone agonist therapy in premenopausal patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer. Bioscientifica Ltd 2019-06-05 /pmc/articles/PMC6599072/ /pubmed/31252399 http://dx.doi.org/10.1530/EC-19-0101 Text en © 2019 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (http://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research
Park, Chan Sub
Choi, Jihye
Seong, Min-Ki
Hong, Sung-Eun
Kim, Jae-Sung
Park, In-Chul
Seol, Hyesil
Noh, Woo Chul
Kim, Hyun-Ah
pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer
title pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer
title_full pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer
title_fullStr pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer
title_full_unstemmed pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer
title_short pS6K1 as an efficacy marker of GnRH agonist with premenopausal breast cancer
title_sort ps6k1 as an efficacy marker of gnrh agonist with premenopausal breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599072/
https://www.ncbi.nlm.nih.gov/pubmed/31252399
http://dx.doi.org/10.1530/EC-19-0101
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