A bibliometric analysis of m6A methylation in viral infection from 2000 to 2022
© 2024. The Author(s)..
BACKGROUND: N6-methyladenosine (m6A) methylation has become an active research area in viral infection, while little bibliometric analysis has been performed. In this study, we aim to visualize hotspots and trends using bibliometric analysis to provide a comprehensive and objective overview of the current research dynamics in this field.
METHODS: The data related to m6A methylation in viral infection were obtained through the Web of Science Core Collection form 2000 to 2022. To reduce bias, the literature search was conducted on December 1, 2022. Bibliometric and visual analyzes were performed using CiteSpace and Bibliometrix package. After screening, 319 qualified records were retrieved.
RESULTS: These publications mainly came from 28 countries led by China and the United States (the US), with the US ranking highest in terms of total link strength.The most common keywords were m6A, COVID-19, epitranscriptomics, METTL3, hepatitis B virus, innate immunity and human immunodeficiency virus 1. The thematic map showed that METTL3, plant viruses, cancer progression and type I interferon (IFN-I) reflected a good development trend and might become a research hotspot in the future, while post-transcriptional modification, as an emerging or declining theme, might not develop well.
CONCLUSIONS: In conclusion, m6A methylation in viral infection is an increasingly important topic in articles. METTL3, plant viruses, cancer progression and IFN-I may still be research hotspots and trends in the future.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:21 |
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| Enthalten in: |
Virology journal - 21(2024), 1 vom: 18. Jan., Seite 20 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Tao, Xing [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Completed 22.01.2024 Date Revised 22.01.2024 published: Electronic Citation Status MEDLINE |
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| doi: |
10.1186/s12985-024-02294-1 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM367293404 |
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| 100 | 1 | |a Tao, Xing |e verfasserin |4 aut | |
| 245 | 1 | 2 | |a A bibliometric analysis of m6A methylation in viral infection from 2000 to 2022 |
| 264 | 1 | |c 2024 | |
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| 500 | |a Date Revised 22.01.2024 | ||
| 500 | |a published: Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a © 2024. The Author(s). | ||
| 520 | |a BACKGROUND: N6-methyladenosine (m6A) methylation has become an active research area in viral infection, while little bibliometric analysis has been performed. In this study, we aim to visualize hotspots and trends using bibliometric analysis to provide a comprehensive and objective overview of the current research dynamics in this field | ||
| 520 | |a METHODS: The data related to m6A methylation in viral infection were obtained through the Web of Science Core Collection form 2000 to 2022. To reduce bias, the literature search was conducted on December 1, 2022. Bibliometric and visual analyzes were performed using CiteSpace and Bibliometrix package. After screening, 319 qualified records were retrieved | ||
| 520 | |a RESULTS: These publications mainly came from 28 countries led by China and the United States (the US), with the US ranking highest in terms of total link strength.The most common keywords were m6A, COVID-19, epitranscriptomics, METTL3, hepatitis B virus, innate immunity and human immunodeficiency virus 1. The thematic map showed that METTL3, plant viruses, cancer progression and type I interferon (IFN-I) reflected a good development trend and might become a research hotspot in the future, while post-transcriptional modification, as an emerging or declining theme, might not develop well | ||
| 520 | |a CONCLUSIONS: In conclusion, m6A methylation in viral infection is an increasingly important topic in articles. METTL3, plant viruses, cancer progression and IFN-I may still be research hotspots and trends in the future | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Bibliometric analysis | |
| 650 | 4 | |a Data visualization | |
| 650 | 4 | |a Methylation | |
| 650 | 4 | |a N6-methyladenosine | |
| 650 | 4 | |a Viral infection | |
| 650 | 7 | |a 6-methyladenine |2 NLM | |
| 650 | 7 | |a W7IBY2BGAX |2 NLM | |
| 650 | 7 | |a Interferon Type I |2 NLM | |
| 650 | 7 | |a METTL3 protein, human |2 NLM | |
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| 650 | 7 | |a Methyltransferases |2 NLM | |
| 650 | 7 | |a EC 2.1.1.- |2 NLM | |
| 650 | 7 | |a Adenine |2 NLM | |
| 650 | 7 | |a JAC85A2161 |2 NLM | |
| 700 | 1 | |a Wang, Gang |e verfasserin |4 aut | |
| 700 | 1 | |a Wei, Wudi |e verfasserin |4 aut | |
| 700 | 1 | |a Su, Jinming |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Xiu |e verfasserin |4 aut | |
| 700 | 1 | |a Shi, Minjuan |e verfasserin |4 aut | |
| 700 | 1 | |a Liao, Yinlu |e verfasserin |4 aut | |
| 700 | 1 | |a Qin, Tongxue |e verfasserin |4 aut | |
| 700 | 1 | |a Wu, Yuting |e verfasserin |4 aut | |
| 700 | 1 | |a Lu, Beibei |e verfasserin |4 aut | |
| 700 | 1 | |a Liang, Hao |e verfasserin |4 aut | |
| 700 | 1 | |a Ye, Li |e verfasserin |4 aut | |
| 700 | 1 | |a Jiang, Junjun |e verfasserin |4 aut | |
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