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Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis

INTRODUCTION: The bibliometric analysis aims to identify research trends in estrogen receptor (ERs) and progesterone receptor (PRs) in prostate cancer (PCa), and also discuss the hotspots and directions of this field. METHODS: 835 publications were sourced from the Web of Science database (WOS) from...

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Autores principales: Liao, Wenqiang, Sui, Xuxia, Hou, Gaoming, Yang, Mei, Lin, Yuxue, Lu, Junjie, Yang, Qingtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288854/
https://www.ncbi.nlm.nih.gov/pubmed/37361598
http://dx.doi.org/10.3389/fonc.2023.1111296
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author Liao, Wenqiang
Sui, Xuxia
Hou, Gaoming
Yang, Mei
Lin, Yuxue
Lu, Junjie
Yang, Qingtao
author_facet Liao, Wenqiang
Sui, Xuxia
Hou, Gaoming
Yang, Mei
Lin, Yuxue
Lu, Junjie
Yang, Qingtao
author_sort Liao, Wenqiang
collection PubMed
description INTRODUCTION: The bibliometric analysis aims to identify research trends in estrogen receptor (ERs) and progesterone receptor (PRs) in prostate cancer (PCa), and also discuss the hotspots and directions of this field. METHODS: 835 publications were sourced from the Web of Science database (WOS) from 2003 to 2022. Citespace, VOSviewer, and Bibliometrix were used for the bibliometric analysis. RESULTS: The number of published publications increased in early years, but declined in the last 5 years. The United States was the leading country in citations, publications, and top institutions. Prostate and Karolinska Institutet were the most publications of journal and institution, respectively. Jan-Ake Gustafsson was the most influential author based on the number of citations/publications. The most cited paper was “Estrogen receptors and human disease” by Deroo BJ, published in the Journal of Clinical Investigation. The most frequently used keywords were PCa (n = 499), gene-expression (n = 291), androgen receptor (AR) (n = 263), and ER (n = 341), while ERb (n = 219) and ERa (n = 215) further emphasized the importance of ER. CONCLUSIONS: This study provides useful guidance that ERa antagonists, ERb agonists, and the combination of estrogen with androgen deprivation therapy (ADT) will potentially serve as a new treatment strategy for PCa. Another interesting topic is relationships between PCa and the function and mechanism of action of PRs subtypes. The outcome will assist scholars in gaining a comprehensive understanding of the current status and trends in the field, and provide inspiration for future research.
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spelling pubmed-102888542023-06-24 Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis Liao, Wenqiang Sui, Xuxia Hou, Gaoming Yang, Mei Lin, Yuxue Lu, Junjie Yang, Qingtao Front Oncol Oncology INTRODUCTION: The bibliometric analysis aims to identify research trends in estrogen receptor (ERs) and progesterone receptor (PRs) in prostate cancer (PCa), and also discuss the hotspots and directions of this field. METHODS: 835 publications were sourced from the Web of Science database (WOS) from 2003 to 2022. Citespace, VOSviewer, and Bibliometrix were used for the bibliometric analysis. RESULTS: The number of published publications increased in early years, but declined in the last 5 years. The United States was the leading country in citations, publications, and top institutions. Prostate and Karolinska Institutet were the most publications of journal and institution, respectively. Jan-Ake Gustafsson was the most influential author based on the number of citations/publications. The most cited paper was “Estrogen receptors and human disease” by Deroo BJ, published in the Journal of Clinical Investigation. The most frequently used keywords were PCa (n = 499), gene-expression (n = 291), androgen receptor (AR) (n = 263), and ER (n = 341), while ERb (n = 219) and ERa (n = 215) further emphasized the importance of ER. CONCLUSIONS: This study provides useful guidance that ERa antagonists, ERb agonists, and the combination of estrogen with androgen deprivation therapy (ADT) will potentially serve as a new treatment strategy for PCa. Another interesting topic is relationships between PCa and the function and mechanism of action of PRs subtypes. The outcome will assist scholars in gaining a comprehensive understanding of the current status and trends in the field, and provide inspiration for future research. Frontiers Media S.A. 2023-06-09 /pmc/articles/PMC10288854/ /pubmed/37361598 http://dx.doi.org/10.3389/fonc.2023.1111296 Text en Copyright © 2023 Liao, Sui, Hou, Yang, Lin, Lu and Yang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Liao, Wenqiang
Sui, Xuxia
Hou, Gaoming
Yang, Mei
Lin, Yuxue
Lu, Junjie
Yang, Qingtao
Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
title Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
title_full Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
title_fullStr Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
title_full_unstemmed Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
title_short Trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
title_sort trends in estrogen and progesterone receptors in prostate cancer: a bibliometric analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288854/
https://www.ncbi.nlm.nih.gov/pubmed/37361598
http://dx.doi.org/10.3389/fonc.2023.1111296
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