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Research trends, hot spots and prospects for necroptosis in the field of neuroscience

There are two types of cell death-apoptosis and necrosis. Apoptosis is cell death regulated by cell signaling pathways, while necrosis has until recently been considered a passive mechanism of cell death caused by environmental pressures. However, recent studies show that necrosis can also be regula...

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Autores principales: Yan, Wei-Tao, Lu, Shuang, Yang, Yan-Di, Ning, Wen-Ya, Cai, Yan, Hu, Xi-Min, Zhang, Qi, Xiong, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323674/
https://www.ncbi.nlm.nih.gov/pubmed/33433494
http://dx.doi.org/10.4103/1673-5374.303032
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author Yan, Wei-Tao
Lu, Shuang
Yang, Yan-Di
Ning, Wen-Ya
Cai, Yan
Hu, Xi-Min
Zhang, Qi
Xiong, Kun
author_facet Yan, Wei-Tao
Lu, Shuang
Yang, Yan-Di
Ning, Wen-Ya
Cai, Yan
Hu, Xi-Min
Zhang, Qi
Xiong, Kun
author_sort Yan, Wei-Tao
collection PubMed
description There are two types of cell death-apoptosis and necrosis. Apoptosis is cell death regulated by cell signaling pathways, while necrosis has until recently been considered a passive mechanism of cell death caused by environmental pressures. However, recent studies show that necrosis can also be regulated by specific cell signaling pathways. This mode of death, termed necroptosis, has been found to be related to the occurrence and development of many diseases. We used bibliometrics to analyze the global output of literature on necroptosis in the field of neuroscience published in the period 2007–2019 to identify research hotspots and prospects. We included 145 necroptosis-related publications and 2239 references published in the Web of Science during 2007–2019. Visualization analysis revealed that the number of publications related to necroptosis has increased year by year, reaching a peak in 2019. China is the country with the largest number of publications. Key word and literature analyses demonstrated that mitochondrial function change, stroke, ischemia/reperfusion and neuroinflammation are likely the research hotspots and future directions of necroptosis research in the nervous system. The relationship between immune response-related factors, damage-associated molecular patterns, pathogen-associated molecular patterns and necroptosis may become a potential research hotspot in the future. Taken together, our findings suggest that although the inherent limitations of bibliometrics may affect the accuracy of the literature-based prediction of research hotspots, the results obtained from the included publications can provide a reference for the study of necroptosis in the field of neuroscience.
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spelling pubmed-83236742021-08-11 Research trends, hot spots and prospects for necroptosis in the field of neuroscience Yan, Wei-Tao Lu, Shuang Yang, Yan-Di Ning, Wen-Ya Cai, Yan Hu, Xi-Min Zhang, Qi Xiong, Kun Neural Regen Res Research Article There are two types of cell death-apoptosis and necrosis. Apoptosis is cell death regulated by cell signaling pathways, while necrosis has until recently been considered a passive mechanism of cell death caused by environmental pressures. However, recent studies show that necrosis can also be regulated by specific cell signaling pathways. This mode of death, termed necroptosis, has been found to be related to the occurrence and development of many diseases. We used bibliometrics to analyze the global output of literature on necroptosis in the field of neuroscience published in the period 2007–2019 to identify research hotspots and prospects. We included 145 necroptosis-related publications and 2239 references published in the Web of Science during 2007–2019. Visualization analysis revealed that the number of publications related to necroptosis has increased year by year, reaching a peak in 2019. China is the country with the largest number of publications. Key word and literature analyses demonstrated that mitochondrial function change, stroke, ischemia/reperfusion and neuroinflammation are likely the research hotspots and future directions of necroptosis research in the nervous system. The relationship between immune response-related factors, damage-associated molecular patterns, pathogen-associated molecular patterns and necroptosis may become a potential research hotspot in the future. Taken together, our findings suggest that although the inherent limitations of bibliometrics may affect the accuracy of the literature-based prediction of research hotspots, the results obtained from the included publications can provide a reference for the study of necroptosis in the field of neuroscience. Wolters Kluwer - Medknow 2021-01-07 /pmc/articles/PMC8323674/ /pubmed/33433494 http://dx.doi.org/10.4103/1673-5374.303032 Text en Copyright: © 2021 Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Yan, Wei-Tao
Lu, Shuang
Yang, Yan-Di
Ning, Wen-Ya
Cai, Yan
Hu, Xi-Min
Zhang, Qi
Xiong, Kun
Research trends, hot spots and prospects for necroptosis in the field of neuroscience
title Research trends, hot spots and prospects for necroptosis in the field of neuroscience
title_full Research trends, hot spots and prospects for necroptosis in the field of neuroscience
title_fullStr Research trends, hot spots and prospects for necroptosis in the field of neuroscience
title_full_unstemmed Research trends, hot spots and prospects for necroptosis in the field of neuroscience
title_short Research trends, hot spots and prospects for necroptosis in the field of neuroscience
title_sort research trends, hot spots and prospects for necroptosis in the field of neuroscience
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323674/
https://www.ncbi.nlm.nih.gov/pubmed/33433494
http://dx.doi.org/10.4103/1673-5374.303032
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