间充质干细胞及其细胞外囊泡靶向和破坏肿瘤的研究进展

IF 3.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Progress in Biophysics & Molecular Biology Pub Date : 2023-03-01 DOI:10.1016/j.pbiomolbio.2023.02.001
Mohsen Karami Fath , Zahra Moayedi Banan , Reza Barati , Omid Mohammadrezakhani , Aliasghar Ghaderi , Ali Hatami , Shamim Ghiabi , Nazanin Zeidi , Katayoon Asgari , Zahra Payandeh , Ghasem Barati
{"title":"间充质干细胞及其细胞外囊泡靶向和破坏肿瘤的研究进展","authors":"Mohsen Karami Fath ,&nbsp;Zahra Moayedi Banan ,&nbsp;Reza Barati ,&nbsp;Omid Mohammadrezakhani ,&nbsp;Aliasghar Ghaderi ,&nbsp;Ali Hatami ,&nbsp;Shamim Ghiabi ,&nbsp;Nazanin Zeidi ,&nbsp;Katayoon Asgari ,&nbsp;Zahra Payandeh ,&nbsp;Ghasem Barati","doi":"10.1016/j.pbiomolbio.2023.02.001","DOIUrl":null,"url":null,"abstract":"<div><p><span>Mesenchymal stem cells (MSCs) have the ability to migrate into tumor sites and release growth factors to modulate the tumor microenvironment. MSC therapy have shown a dual role in cancers, promoting or inhibiting. However, MSCs could be used as a carrier of anticancer agents for targeted tumor therapy. Recent technical improvements also allow engineering MSCs to improve tumor-targeting properties, protect anticancer agents, and decrease the cytotoxicity of drugs. While some of MSC functions are mediated through their </span>secretome, MSCs-derived extracellular vesicles (EVs) are also proposed as a possible viechle for cancer therapy. EVs allow efficient loading of anticancer agents and have an intrinsic ability to target tumor cells, making them suitable for targeted therapy of tumors. In addition, the specificity and selectivity of EVs to the tumor sites could be enhanced by surface modification. In this review, we addressed the current approaches used for engineering MSCs and EVs to effectively target tumor sites and deliver anticancer agents.</p></div>","PeriodicalId":54554,"journal":{"name":"Progress in Biophysics & Molecular Biology","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Recent advancements to engineer mesenchymal stem cells and their extracellular vesicles for targeting and destroying tumors\",\"authors\":\"Mohsen Karami Fath ,&nbsp;Zahra Moayedi Banan ,&nbsp;Reza Barati ,&nbsp;Omid Mohammadrezakhani ,&nbsp;Aliasghar Ghaderi ,&nbsp;Ali Hatami ,&nbsp;Shamim Ghiabi ,&nbsp;Nazanin Zeidi ,&nbsp;Katayoon Asgari ,&nbsp;Zahra Payandeh ,&nbsp;Ghasem Barati\",\"doi\":\"10.1016/j.pbiomolbio.2023.02.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Mesenchymal stem cells (MSCs) have the ability to migrate into tumor sites and release growth factors to modulate the tumor microenvironment. MSC therapy have shown a dual role in cancers, promoting or inhibiting. However, MSCs could be used as a carrier of anticancer agents for targeted tumor therapy. Recent technical improvements also allow engineering MSCs to improve tumor-targeting properties, protect anticancer agents, and decrease the cytotoxicity of drugs. While some of MSC functions are mediated through their </span>secretome, MSCs-derived extracellular vesicles (EVs) are also proposed as a possible viechle for cancer therapy. EVs allow efficient loading of anticancer agents and have an intrinsic ability to target tumor cells, making them suitable for targeted therapy of tumors. In addition, the specificity and selectivity of EVs to the tumor sites could be enhanced by surface modification. In this review, we addressed the current approaches used for engineering MSCs and EVs to effectively target tumor sites and deliver anticancer agents.</p></div>\",\"PeriodicalId\":54554,\"journal\":{\"name\":\"Progress in Biophysics & Molecular Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2023-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Progress in Biophysics & Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0079610723000135\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in Biophysics & Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0079610723000135","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

间充质干细胞(MSCs)具有迁移到肿瘤部位并释放生长因子以调节肿瘤微环境的能力。MSC治疗在癌症中显示出促进或抑制的双重作用。然而,间充质干细胞可作为抗癌剂的载体用于靶向肿瘤治疗。最近的技术进步也使工程MSC能够改善肿瘤靶向特性,保护抗癌药物,并降低药物的细胞毒性。虽然一些MSC功能是通过其分泌体介导的,但MSC衍生的细胞外小泡(EVs)也被认为是癌症治疗的可能途径。EVs允许有效负载抗癌剂,并具有靶向肿瘤细胞的内在能力,使其适合肿瘤的靶向治疗。此外,EVs对肿瘤部位的特异性和选择性可以通过表面修饰来增强。在这篇综述中,我们介绍了目前用于工程MSCs和EVs以有效靶向肿瘤部位并递送抗癌药物的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Recent advancements to engineer mesenchymal stem cells and their extracellular vesicles for targeting and destroying tumors

Mesenchymal stem cells (MSCs) have the ability to migrate into tumor sites and release growth factors to modulate the tumor microenvironment. MSC therapy have shown a dual role in cancers, promoting or inhibiting. However, MSCs could be used as a carrier of anticancer agents for targeted tumor therapy. Recent technical improvements also allow engineering MSCs to improve tumor-targeting properties, protect anticancer agents, and decrease the cytotoxicity of drugs. While some of MSC functions are mediated through their secretome, MSCs-derived extracellular vesicles (EVs) are also proposed as a possible viechle for cancer therapy. EVs allow efficient loading of anticancer agents and have an intrinsic ability to target tumor cells, making them suitable for targeted therapy of tumors. In addition, the specificity and selectivity of EVs to the tumor sites could be enhanced by surface modification. In this review, we addressed the current approaches used for engineering MSCs and EVs to effectively target tumor sites and deliver anticancer agents.

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
Progress in Biophysics & Molecular Biology
Progress in Biophysics & Molecular Biology 生物-生化与分子生物学
CiteScore
8.60
自引率
7.90%
发文量
85
审稿时长
85 days
期刊介绍: Progress in Biophysics & Molecular Biology is an international review journal and covers the ground between the physical and biological sciences since its launch in 1950. It indicates to the physicist the great variety of unsolved problems awaiting attention in biology and medicine. The biologist and biochemist will find that this journal presents new and stimulating ideas and novel approaches to studying and influencing structural and functional properties of the living organism. This journal will be of particular interest to biophysicists, biologists, biochemists, cell physiologists, systems biologists, and molecular biologists.
期刊最新文献
A physical perspective on lithium therapy. Editorial Board Computational approaches for modeling and structural design of biological systems: A comprehensive review Recent progress of mechanosensitive mechanism on breast cancer Editorial Board
×
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