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神经科学领域坏死性凋亡的研究趋势、热点及展望

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

作者信息

Yan Wei-Tao, Lu Shuang, Yang Yan-Di, Ning Wen-Ya, Cai Yan, Hu Xi-Min, Zhang Qi, Xiong Kun

机构信息

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan Province, China.

Third Xiangya Hospital of Central South University, Changsha, Hunan Province, China.

出版信息

Neural Regen Res. 2021 Aug;16(8):1628-1637. doi: 10.4103/1673-5374.303032.

DOI:10.4103/1673-5374.303032
PMID:33433494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8323674/
Abstract

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.

摘要

细胞死亡有两种类型——凋亡和坏死。凋亡是由细胞信号通路调节的细胞死亡,而坏死直到最近一直被认为是由环境压力导致的一种被动的细胞死亡机制。然而,最近的研究表明,坏死也可由特定的细胞信号通路调节。这种死亡模式被称为坏死性凋亡,已被发现与许多疾病的发生和发展有关。我们使用文献计量学方法分析了2007年至2019年期间发表在神经科学领域的关于坏死性凋亡的全球文献产出,以确定研究热点和前景。我们纳入了2007年至2019年期间发表在科学网的145篇与坏死性凋亡相关的出版物及2239条参考文献。可视化分析显示,与坏死性凋亡相关的出版物数量逐年增加,在2019年达到峰值。中国是发表数量最多的国家。关键词和文献分析表明,线粒体功能改变、中风、缺血/再灌注和神经炎症可能是神经系统坏死性凋亡研究的热点和未来方向。免疫反应相关因子、损伤相关分子模式、病原体相关分子模式与坏死性凋亡之间的关系可能成为未来潜在的研究热点。综上所述,我们的研究结果表明,尽管文献计量学的固有局限性可能会影响基于文献对研究热点预测的准确性,但从纳入的出版物中获得的结果可为神经科学领域坏死性凋亡的研究提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/e99669d5479c/NRR-16-1628-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/53313bf384d0/NRR-16-1628-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/ef24dfb08f18/NRR-16-1628-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/53980f0a7cdb/NRR-16-1628-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/2642b226f757/NRR-16-1628-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/ad858f8f783f/NRR-16-1628-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/5726da2b4860/NRR-16-1628-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/e99669d5479c/NRR-16-1628-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/53313bf384d0/NRR-16-1628-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/df3533e7a0c7/NRR-16-1628-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/ef24dfb08f18/NRR-16-1628-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/ea64a9ef6b0d/NRR-16-1628-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/53980f0a7cdb/NRR-16-1628-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/2642b226f757/NRR-16-1628-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/ad858f8f783f/NRR-16-1628-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/5726da2b4860/NRR-16-1628-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c155/8323674/e99669d5479c/NRR-16-1628-g010.jpg

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