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类器官,一种用于监测癌症血管生成的有效的临床前筛选平台。

Tumoroids, a valid preclinical screening platform for monitoring cancer angiogenesis.

机构信息

Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Stem Cell Res Ther. 2024 Aug 26;15(1):267. doi: 10.1186/s13287-024-03880-4.

DOI:10.1186/s13287-024-03880-4
PMID:39183337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11346257/
Abstract

In recent years, biologists and clinicians have witnessed prominent advances in in vitro 3D culture techniques related to biomimetic human/animal tissue analogs. Numerous data have confirmed that unicellular and multicellular (tumoroids) tumor spheroids with dense native cells in certain matrices are sensitive and valid analytical tools for drug screening, cancer cell dynamic growth, behavior, etc. in laboratory settings. Angiogenesis/vascularization is a very critical biological phenomenon to support oxygen and nutrients to tumor cells within the deep layer of solid masses. It has been shown that endothelial cell (EC)-incorporated or -free spheroid/tumoroid systems provide a relatively reliable biological platform for monitoring the formation of nascent blood vessels in micron/micrometer scales. Besides, the paracrine angiogenic activity of cells within the spheroid/tumoroid systems can be monitored after being treated with different therapeutic approaches. Here, we aimed to collect recent advances and findings related to the monitoring of cancer angiogenesis using unicellular and multicellular tumor spheroids. Vascularized spheroids/tumoroids can help us in the elucidation of mechanisms related to cancer formation, development, and metastasis by monitoring the main influencing factors.

摘要

近年来,生物学家和临床医生见证了与仿生人体/动物组织类似物相关的体外 3D 培养技术的显著进步。大量数据证实,具有密集天然细胞的单细胞和多细胞(类器官)肿瘤球体在某些基质中是药物筛选、癌细胞动态生长、行为等的敏感和有效的分析工具。血管生成/血管化是支持实体瘤深层肿瘤细胞的氧气和营养物质的非常关键的生物学现象。已经表明,内皮细胞(EC)掺入或不含球体/类器官系统为监测新生血管在微米/微米尺度上的形成提供了相对可靠的生物学平台。此外,在用不同治疗方法处理后,可以监测球体/类器官系统内细胞的旁分泌血管生成活性。在这里,我们旨在收集使用单细胞和多细胞肿瘤球体监测癌症血管生成的最新进展和发现。血管化球体/类器官可以通过监测主要影响因素,帮助我们阐明与癌症形成、发展和转移相关的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/78c6d03ea9e0/13287_2024_3880_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/e5ce70264171/13287_2024_3880_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/b431a91f7b1f/13287_2024_3880_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/226ae8317364/13287_2024_3880_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/0efc86e6e5fb/13287_2024_3880_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/7b7de623b132/13287_2024_3880_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/78c6d03ea9e0/13287_2024_3880_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/e5ce70264171/13287_2024_3880_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/b431a91f7b1f/13287_2024_3880_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/226ae8317364/13287_2024_3880_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/0efc86e6e5fb/13287_2024_3880_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/7b7de623b132/13287_2024_3880_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/11346257/78c6d03ea9e0/13287_2024_3880_Fig6_HTML.jpg

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A Molecular Perspective on HIF-1α and Angiogenic Stimulator Networks and Their Role in Solid Tumors: An Update.
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