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Research landscape and frontiers of non-alcoholic steatohepatitis-associated hepatocellular carcinoma: a bibliometric and visual analysis.

作者信息

Gao Bowen, Chen Zhiheng, Shi Meijie, Mo Yousheng, Xiao Huanming, Xie Yubao, Lin Ming, Chi Xiaoling

机构信息

The Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou, China.

Department of Hepatology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, China.

出版信息

Front Pharmacol. 2023 Sep 12;14:1240649. doi: 10.3389/fphar.2023.1240649. eCollection 2023.


DOI:10.3389/fphar.2023.1240649
PMID:37771721
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10523561/
Abstract

Due to the widespread prevalence of caloric excess and sedentary behavior on a global scale, there is a growing body of epidemiological evidence indicating that non-alcoholic steatohepatitis (NASH) has rapidly become a leading aetiology underlying of hepatocellular carcinoma (HCC). In light of the escalating incidence of NASH-associated HCC (NASH-HCC), it is imperative to mitigate the impending burden. While there has been an increase in global awareness regarding this issue, it has yet to be examined from a bibliometric standpoint. Therefore, this study seeks to provide a comprehensive bibliometric analysis to characterize the evolution of this field. The present study utilized the Web of Science Core Collection (WoSCC) to identify publications pertaining to NASH-HCC over the past 2 decades. Employing Vosviewer 1.6.19, CiteSpace 6.2.R2, and the Analysis Platform of Bibliometrics, the study conducted an analysis of various dimensions including the quantity of publications, countries, institutions, journals, authors, co-references, keywords, and trend topics in this field. A comprehensive analysis of 3,679 publications pertaining to NASH-HCC, published between 1 January 2002 and 1 April 2023, was conducted. The field in question experienced a rapid increase in publications, with the United States serving as the central hub. Collaboration between institutions was more extensive than that between countries. Notably, HEPATOLOGY ( = 30,168) emerged as the most impactful journal, and Zobair M. Younossi ( = 10,025) as the most frequently cited author in co-citations. The most commonly cited references were KLEINER DE, 2005, HEPATOLOGY ( = 630), followed by YOUNOSSI ZM, 2016, HEPATOLOGY ( = 493). The author keywords were categorized into three distinct clusters, namely, Cluster 1 (Mechanism), Cluster 2 (Factors), and Cluster 3 (Diagnosis). Analysis of high-frequency co-occurring keywords and topical trends revealed emphasis on molecular mechanisms in current research. "macrophages" and "tumor microenvironment" were active research hotspots at present in this field. A bibliometric analysis was performed for the first time on publications pertaining to non-alcoholic steatohepatitis-hepatocellular carcinoma, uncovering co-research networks, developmental trends, and current research hotspots. The emerging frontiers of this field focused on the macrophages and tumor microenvironment, especially the tumor-associated macrophages, offering a fresh perspective for future research directions.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/d131a6cc2d58/fphar-14-1240649-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/a3d2ff3fd4db/fphar-14-1240649-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/df3e571a7bba/fphar-14-1240649-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/c7f9dd9ef5ff/fphar-14-1240649-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/7c19fa628dcd/fphar-14-1240649-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/51555dbd6a44/fphar-14-1240649-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/d81f1ccd1a1d/fphar-14-1240649-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/5790b8c61155/fphar-14-1240649-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/d131a6cc2d58/fphar-14-1240649-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/a3d2ff3fd4db/fphar-14-1240649-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/df3e571a7bba/fphar-14-1240649-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/c7f9dd9ef5ff/fphar-14-1240649-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/7c19fa628dcd/fphar-14-1240649-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/51555dbd6a44/fphar-14-1240649-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/d81f1ccd1a1d/fphar-14-1240649-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/5790b8c61155/fphar-14-1240649-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d6/10523561/d131a6cc2d58/fphar-14-1240649-g008.jpg

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本文引用的文献

[1]
Trends in NLRP3 inflammasome research in ischemic stroke from 2011 to 2022: A bibliometric analysis.

CNS Neurosci Ther. 2023-10

[2]
Nonalcoholic steatohepatitis-related hepatocellular carcinoma: pathogenesis and treatment.

Nat Rev Gastroenterol Hepatol. 2023-8

[3]
A bibliometric analysis of primary immune thrombocytopenia from 2011 to 2021.

Br J Haematol. 2023-6

[4]
Crosstalk between extracellular vesicles and tumor-associated macrophage in the tumor microenvironment.

Cancer Lett. 2023-1-1

[5]
CD36-mediated metabolic crosstalk between tumor cells and macrophages affects liver metastasis.

Nat Commun. 2022-10-2

[6]
NASH and Hepatocellular Carcinoma: Immunology and Immunotherapy.

Clin Cancer Res. 2023-2-1

[7]
Liver macrophages in health and disease.

Immunity. 2022-9-13

[8]
Tumor-associated macrophages in liver cancer: From mechanisms to therapy.

Cancer Commun (Lond). 2022-11

[9]
Macrophages as tools and targets in cancer therapy.

Nat Rev Drug Discov. 2022-11

[10]
CXCR2 inhibition enables NASH-HCC immunotherapy.

Gut. 2022-4-27

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