肿瘤衍生的纳米种子为转移性嗜器官性调节土壤

IF 12.1 1区 医学 Q1 ONCOLOGY Seminars in cancer biology Pub Date : 2023-08-01 DOI:10.1016/j.semcancer.2023.05.003
Mengying Hu , Candia M. Kenific , Nancy Boudreau, David Lyden
{"title":"肿瘤衍生的纳米种子为转移性嗜器官性调节土壤","authors":"Mengying Hu ,&nbsp;Candia M. Kenific ,&nbsp;Nancy Boudreau,&nbsp;David Lyden","doi":"10.1016/j.semcancer.2023.05.003","DOIUrl":null,"url":null,"abstract":"<div><p><span>Primary tumors secrete a variety of factors to turn distant microenvironments into favorable and fertile ‘soil’ for subsequent metastases. Among these ‘seeding’ factors that initiate pre-metastatic niche (PMN) formation, tumor-derived extracellular vesicles (EVs) are of particular interest as tumor EVs can direct organotropism depending on their surface integrin<span> profiles. In addition, EVs also contain versatile, bioactive cargo, which include proteins, metabolites, lipids, </span></span>RNA<span>, and DNA<span> fragments. The cargo incorporated into EVs is collectively shed from cancer cells and cancer-associated stromal cells. Increased understanding of how tumor EVs promote PMN establishment and detection of EVs in bodily fluids highlight how tumor EVs could serve as potential diagnostic and prognostic biomarkers, as well as provide a therapeutic target for metastasis prevention. This review focuses on tumor-derived EVs and how they direct organotropism and subsequently modulate stromal and immune microenvironments at distal sites to facilitate PMN formation. We also outline the progress made thus far towards clinical applications of tumor EVs.</span></span></p></div>","PeriodicalId":21594,"journal":{"name":"Seminars in cancer biology","volume":"93 ","pages":"Pages 70-82"},"PeriodicalIF":12.1000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362948/pdf/","citationCount":"3","resultStr":"{\"title\":\"Tumor-derived nanoseeds condition the soil for metastatic organotropism\",\"authors\":\"Mengying Hu ,&nbsp;Candia M. Kenific ,&nbsp;Nancy Boudreau,&nbsp;David Lyden\",\"doi\":\"10.1016/j.semcancer.2023.05.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Primary tumors secrete a variety of factors to turn distant microenvironments into favorable and fertile ‘soil’ for subsequent metastases. Among these ‘seeding’ factors that initiate pre-metastatic niche (PMN) formation, tumor-derived extracellular vesicles (EVs) are of particular interest as tumor EVs can direct organotropism depending on their surface integrin<span> profiles. In addition, EVs also contain versatile, bioactive cargo, which include proteins, metabolites, lipids, </span></span>RNA<span>, and DNA<span> fragments. The cargo incorporated into EVs is collectively shed from cancer cells and cancer-associated stromal cells. Increased understanding of how tumor EVs promote PMN establishment and detection of EVs in bodily fluids highlight how tumor EVs could serve as potential diagnostic and prognostic biomarkers, as well as provide a therapeutic target for metastasis prevention. This review focuses on tumor-derived EVs and how they direct organotropism and subsequently modulate stromal and immune microenvironments at distal sites to facilitate PMN formation. We also outline the progress made thus far towards clinical applications of tumor EVs.</span></span></p></div>\",\"PeriodicalId\":21594,\"journal\":{\"name\":\"Seminars in cancer biology\",\"volume\":\"93 \",\"pages\":\"Pages 70-82\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2023-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362948/pdf/\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Seminars in cancer biology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1044579X23000779\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminars in cancer biology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1044579X23000779","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 3

摘要

原发性肿瘤分泌多种因子,将远处的微环境转化为后续转移的有利肥沃的“土壤”。在这些启动转移前小生境(PMN)形成的“种子”因子中,肿瘤衍生的细胞外小泡(EVs)尤其令人感兴趣,因为肿瘤EVs可以根据其表面整合素谱指导器官向性。此外,电动汽车还含有多种生物活性物质,包括蛋白质、代谢产物、脂质、RNA和DNA片段。纳入电动汽车的货物是由癌症细胞和癌症相关基质细胞共同脱落的。对肿瘤EVs如何促进PMN的建立和体液中EVs的检测的深入了解,突出了肿瘤EVs可以作为潜在的诊断和预后生物标志物,并为预防转移提供治疗靶点。这篇综述的重点是肿瘤衍生的EVs,以及它们如何引导器官向性,并随后调节远端部位的基质和免疫微环境,以促进PMN的形成。我们还概述了迄今为止在肿瘤EVs临床应用方面取得的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Tumor-derived nanoseeds condition the soil for metastatic organotropism

Primary tumors secrete a variety of factors to turn distant microenvironments into favorable and fertile ‘soil’ for subsequent metastases. Among these ‘seeding’ factors that initiate pre-metastatic niche (PMN) formation, tumor-derived extracellular vesicles (EVs) are of particular interest as tumor EVs can direct organotropism depending on their surface integrin profiles. In addition, EVs also contain versatile, bioactive cargo, which include proteins, metabolites, lipids, RNA, and DNA fragments. The cargo incorporated into EVs is collectively shed from cancer cells and cancer-associated stromal cells. Increased understanding of how tumor EVs promote PMN establishment and detection of EVs in bodily fluids highlight how tumor EVs could serve as potential diagnostic and prognostic biomarkers, as well as provide a therapeutic target for metastasis prevention. This review focuses on tumor-derived EVs and how they direct organotropism and subsequently modulate stromal and immune microenvironments at distal sites to facilitate PMN formation. We also outline the progress made thus far towards clinical applications of tumor EVs.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Seminars in cancer biology
Seminars in cancer biology 医学-肿瘤学
CiteScore
26.80
自引率
4.10%
发文量
347
审稿时长
15.1 weeks
期刊介绍: Seminars in Cancer Biology (YSCBI) is a specialized review journal that focuses on the field of molecular oncology. Its primary objective is to keep scientists up-to-date with the latest developments in this field. The journal adopts a thematic approach, dedicating each issue to an important topic of interest to cancer biologists. These topics cover a range of research areas, including the underlying genetic and molecular causes of cellular transformation and cancer, as well as the molecular basis of potential therapies. To ensure the highest quality and expertise, every issue is supervised by a guest editor or editors who are internationally recognized experts in the respective field. Each issue features approximately eight to twelve authoritative invited reviews that cover various aspects of the chosen subject area. The ultimate goal of each issue of YSCBI is to offer a cohesive, easily comprehensible, and engaging overview of the selected topic. The journal strives to provide scientists with a coordinated and lively examination of the latest developments in the field of molecular oncology.
期刊最新文献
Mechanisms and strategies of immunosenescence effects on non-small cell lung cancer (NSCLC) treatment: A comprehensive analysis and future directions. Fungi, immunosenescence and cancer. Multi-omic markers of intraductal papillary mucinous neoplasms progression into pancreatic cancer. Organoids, tissue slices and organotypic cultures: Advancing our understanding of pancreatic ductal adenocarcinoma through in vitro and ex vivo models. Cancer cell populations.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1