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Bibliometric analysis of toll-like receptor agonists associated with cancer therapy

BACKGROUND: Toll-like receptors (TLRs), a family of innate pattern-recognition receptors, have been exploited as a target for antitumor strategy. An increasing number of TLR agonists, serving as immunotherapeutics or vaccine adjuvants, were developed. This study aimed at exploring the status and tre...

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Detalles Bibliográficos
Autores principales: Li, Wei, Wan, Li, Duan, Shaojun, Xu, Jingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8735774/
https://www.ncbi.nlm.nih.gov/pubmed/35029915
http://dx.doi.org/10.1097/MD.0000000000028520
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author Li, Wei
Wan, Li
Duan, Shaojun
Xu, Jingjing
author_facet Li, Wei
Wan, Li
Duan, Shaojun
Xu, Jingjing
author_sort Li, Wei
collection PubMed
description BACKGROUND: Toll-like receptors (TLRs), a family of innate pattern-recognition receptors, have been exploited as a target for antitumor strategy. An increasing number of TLR agonists, serving as immunotherapeutics or vaccine adjuvants, were developed. This study aimed at exploring the status and trend of current researches on TLR agonists through bibliometric analysis. METHODS: Original publications on TLR agonists were collected from the Web of Science Core Collection. Data were analyzed in terms of publication outputs, journals, countries, institutions, authors, co-authorship, co-citation, research hotspots, and evolution trends through VOSviewer and CiteSpace. RESULTS: A total of 1914 TLR agonists-related articles, published in 612 academic journals between 2000 and 2019, were enrolled in the study. The Journal of Immunology published the most publications, followed by PLoS One and Blood. The USA that is in possession of the largest number of articles and the most extensive cooperators was the most leading country in this field. University of Minnesota ranked the first in terms of paper totality, but its average citations ranking was lower than University of Pennsylvania. Gudkov AV was the most productive author, whose team reported a TLR5 agonist that had radioprotective activity in mouse and primate models in 2008. The paper of Akira Shizuo, professor of Osaka University, was widely cited by international peers. The research trend of TLR agonists has undergone 3 periods: mechanisms of TLR signalings in immunotherapy (2000–2010), discovery of TLR agonists (2011–2014), application, therapeutic evaluation, and drug design of TLR agonists (2015–2019). CONCLUSION: This study provides investigators a landscape of TLR agonists research from the perspective of bibliometrics.
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spelling pubmed-87357742022-01-11 Bibliometric analysis of toll-like receptor agonists associated with cancer therapy Li, Wei Wan, Li Duan, Shaojun Xu, Jingjing Medicine (Baltimore) 5700 BACKGROUND: Toll-like receptors (TLRs), a family of innate pattern-recognition receptors, have been exploited as a target for antitumor strategy. An increasing number of TLR agonists, serving as immunotherapeutics or vaccine adjuvants, were developed. This study aimed at exploring the status and trend of current researches on TLR agonists through bibliometric analysis. METHODS: Original publications on TLR agonists were collected from the Web of Science Core Collection. Data were analyzed in terms of publication outputs, journals, countries, institutions, authors, co-authorship, co-citation, research hotspots, and evolution trends through VOSviewer and CiteSpace. RESULTS: A total of 1914 TLR agonists-related articles, published in 612 academic journals between 2000 and 2019, were enrolled in the study. The Journal of Immunology published the most publications, followed by PLoS One and Blood. The USA that is in possession of the largest number of articles and the most extensive cooperators was the most leading country in this field. University of Minnesota ranked the first in terms of paper totality, but its average citations ranking was lower than University of Pennsylvania. Gudkov AV was the most productive author, whose team reported a TLR5 agonist that had radioprotective activity in mouse and primate models in 2008. The paper of Akira Shizuo, professor of Osaka University, was widely cited by international peers. The research trend of TLR agonists has undergone 3 periods: mechanisms of TLR signalings in immunotherapy (2000–2010), discovery of TLR agonists (2011–2014), application, therapeutic evaluation, and drug design of TLR agonists (2015–2019). CONCLUSION: This study provides investigators a landscape of TLR agonists research from the perspective of bibliometrics. Lippincott Williams & Wilkins 2022-01-07 /pmc/articles/PMC8735774/ /pubmed/35029915 http://dx.doi.org/10.1097/MD.0000000000028520 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 5700
Li, Wei
Wan, Li
Duan, Shaojun
Xu, Jingjing
Bibliometric analysis of toll-like receptor agonists associated with cancer therapy
title Bibliometric analysis of toll-like receptor agonists associated with cancer therapy
title_full Bibliometric analysis of toll-like receptor agonists associated with cancer therapy
title_fullStr Bibliometric analysis of toll-like receptor agonists associated with cancer therapy
title_full_unstemmed Bibliometric analysis of toll-like receptor agonists associated with cancer therapy
title_short Bibliometric analysis of toll-like receptor agonists associated with cancer therapy
title_sort bibliometric analysis of toll-like receptor agonists associated with cancer therapy
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8735774/
https://www.ncbi.nlm.nih.gov/pubmed/35029915
http://dx.doi.org/10.1097/MD.0000000000028520
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