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外泌体与炎症反应对肿瘤的影响:基于 CiteSpace 和 VOSviewer 的文献计量学研究与可视化分析。

Effects of exosomes and inflammatory response on tumor: a bibliometrics study and visualization analysis via CiteSpace and VOSviewer.

机构信息

North China University of Science and Technology (Hebei Key Laboratory for Chronic Diseases), Tangshan, China.

North China University of Science and Technology Affiliated Hospital, Tangshan, China.

出版信息

J Cancer Res Clin Oncol. 2024 Aug 30;150(8):405. doi: 10.1007/s00432-024-05915-y.

Abstract

BACKGROUND

Tumor is a new organism formed by abnormal hyperplasia of local tissue cells under the action of various tumorigenic factors. Inflammation plays a decisive role in inducing tumorigenesis, promoting tumor development, invasion and migration. More and more evidence indicate that exosomes are involved in regulating the formation of tumor microenvironment in the process of proinflammatory carcinogenesis, leading to the stimulation of anti-tumor immune response or systemic immunosuppression, and exosomes play a crucial role in the development of tumor.

METHODS

The articles on tumor-derived exosomes and inflammatory responses from January 2005 to January 2024 were collected through Web of Science (WOS), and the inclusion criteria were "Article", "Review Article" and "Early Access". Articles obtained after excluding "Book Chapters", "Editorial Material", "Proceeding Paper", "Meeting Abstract" and "Retracted Publication". Bibliometrics and visualization analysis were carried out on the obtained articles using CiteSpace6.2.R6 and VOSviewer1.6.20.

RESULTS

Total of 703 articles were included. The number of published documents showed a fluctuating growth trend year by year. A total of 61 countries have participated in the research on the effects of exosomes and inflammatory responses on tumors, among which China and the United States have the largest influence in this field. The obtained articles have been published in 60 journals around the world, among which PLOS ONE and NAT REV IMMUNOL are the journals with the most published articles and the highest co-citations respectively. The article from French author THERY C was cited the most (202 times). As a major researcher on the basic function of exosomes, THERY C established the gold standard for extraction, separation and identification of exosomes, and found that exosomes promote tumor metastasis through direct regulation of miRNA. Her research has had a huge impact on the field. Keyword co-occurrence analysis indicate that extracellular vesicles, inflammation, cancer, miRNAs, mesenchymal stem cells, drug delivery, gastric cancer and circulating endothelial microparticles are the research hotspot at present stage. The main keywords of the cluster analysis show that extracellular vesicles, human papilloma virus, myeloid cells, tumor macro-environment are the current research hotspots and frontier. The research hotspots have developed over time from the time chart of keywords and clustering, especially after 2016, exosomes have established extensive links with drug delivery, cancer treatment, inflammatory response and other fields. Tumor-derived exosomes stimulate receptor cells to secrete pro-inflammatory cytokines and growth factors, enabling immune and inflammatory cells to perceive the intracellular environment of cancer cells even when cancer cells do not express any tumor-specific antigens. For example, in anoxic environment, cancer cells can secrete exosomes containing pro-inflammatory factors to promote the invasion and metastasis of cancer cells. In the complex tumor microenvironment, both tumor cells and various stromal cells will secrete specific exosomes, and promote the development of tumors through various ways, so that tumor cells have drug resistance, and bring adverse effects on the clinical treatment of tumor patients. MicroRNAs and long noncoding RNA as hot keywords play important roles in regulating and mediating tumor development, and their specificity makes them important biomarkers for cancer prediction and diagnosis. Highlighting word analysis shows that microRNAs secreted by leukemia patients can effectively promote the proliferation of malignant cells and the development of cardiovascular diseases. At the same time, exosomes can induce the secretion of some microRNAs in patients, leading to cardiac repair and regeneration. Therefore, the detection and screening of microRNAs plays a crucial role in predicting the incidence of cardiovascular diseases in patients.

CONCLUSION

Exosomes have attracted increasing attention due to their significant heterogeneity and ability to regulate the tumor immune microenvironment. However, tumor cell-derived exosomes accelerate tumor progression by enhancing immunosuppression and inflammation, increasing oxidative stress, and promoting angiogenesis, which may lead to poor prognosis.

摘要

背景

肿瘤是在各种致癌因素作用下局部组织细胞异常增生形成的新生物。炎症在诱导肿瘤发生、促进肿瘤发展、侵袭和迁移中起决定性作用。越来越多的证据表明,外泌体在促炎致癌发生过程中参与调节肿瘤微环境的形成,导致抗肿瘤免疫反应的刺激或全身免疫抑制,外泌体在肿瘤的发展中起着至关重要的作用。

方法

通过 Web of Science(WOS)收集了 2005 年 1 月至 2024 年 1 月关于肿瘤源性外泌体和炎症反应的文章,纳入标准为“文章”、“综述文章”和“早期访问”。排除“图书章节”、“编辑材料”、“进展论文”、“会议摘要”和“撤回出版物”后获得的文章。使用 CiteSpace6.2.R6 和 VOSviewer1.6.20 对获得的文章进行文献计量学和可视化分析。

结果

共纳入 703 篇文章。发表文献数量呈逐年波动增长趋势。共有 61 个国家参与了外泌体和炎症反应对肿瘤影响的研究,其中中国和美国在这一领域的影响力最大。获得的文章已在全球 60 种期刊上发表,其中 PLOS ONE 和 NAT REV IMMUNOL 分别是发表文章最多和被引次数最多的期刊。来自法国作者 THERY C 的文章被引次数最多(202 次)。作为外泌体基本功能的主要研究者,THERY C 建立了外泌体提取、分离和鉴定的金标准,并发现外泌体通过直接调节 miRNA 促进肿瘤转移。她的研究对外泌体领域产生了巨大影响。关键词共现分析表明,目前的研究热点是细胞外囊泡、炎症、癌症、miRNAs、间充质干细胞、药物输送、胃癌和循环内皮微颗粒。聚类分析的主要关键词显示,细胞外囊泡、人乳头瘤病毒、髓样细胞、肿瘤宏观环境是当前的研究热点和前沿。随着时间的推移,从关键词和聚类的时间图可以看出,研究热点已经从细胞外囊泡与药物输送、癌症治疗、炎症反应等领域建立了广泛的联系。肿瘤源性外泌体刺激受体细胞分泌促炎细胞因子和生长因子,使免疫和炎症细胞即使在癌细胞不表达任何肿瘤特异性抗原时也能感知癌细胞的细胞内环境。例如,在缺氧环境中,癌细胞可以分泌含有促炎因子的外泌体,促进癌细胞的侵袭和转移。在复杂的肿瘤微环境中,肿瘤细胞和各种基质细胞都会分泌特定的外泌体,通过各种方式促进肿瘤的发展,使肿瘤细胞具有耐药性,并给肿瘤患者的临床治疗带来不良影响。miRNAs 和长非编码 RNA 作为热门关键词,在调节和介导肿瘤发展中发挥着重要作用,其特异性使其成为癌症预测和诊断的重要生物标志物。突出词分析表明,白血病患者分泌的 microRNAs 可有效促进恶性细胞的增殖和心血管疾病的发展。同时,外泌体可以诱导患者分泌一些 microRNAs,导致心脏修复和再生。因此,microRNAs 的检测和筛选对预测患者心血管疾病的发病率至关重要。

结论

由于其显著的异质性和调节肿瘤免疫微环境的能力,外泌体引起了越来越多的关注。然而,肿瘤细胞来源的外泌体通过增强免疫抑制和炎症、增加氧化应激以及促进血管生成来加速肿瘤的进展,这可能导致预后不良。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e30/11362500/12d715d2f58c/432_2024_5915_Fig1_HTML.jpg

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