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3D尤文肉瘤模型中玻连蛋白作用的表征:两种细胞系的数字显微镜分析

Characterization of Vitronectin Effect in 3D Ewing Sarcoma Models: A Digital Microscopic Analysis of Two Cell Lines.

作者信息

López-Carrasco Amparo, Parra-Haro Karina, Vieco-Martí Isaac, Granados-Aparici Sofía, Díaz-Martín Juan, Salguero-Aranda Carmen, Acevedo-León Delia, de Álava Enrique, Navarro Samuel, Noguera Rosa

机构信息

Incliva Biomedical Health Research Institute, 46010 Valencia, Spain.

Centro de Investigación Biomédica en Red de Cáncer, Instituto de Salud Carlos III, 28029 Madrid, Spain.

出版信息

Cancers (Basel). 2024 Sep 30;16(19):3347. doi: 10.3390/cancers16193347.

Abstract

Ewing sarcoma (ES) is an aggressive bone and soft-tissue pediatric cancer. High vitronectin (VN) expression has been associated with poor prognosis in other cancers, and we aimed to determine the utility of this extracellular matrix glycoprotein as a biomarker of aggressiveness in ES. Silk fibroin plus gelatin-tyramine hydrogels (HGs) were fabricated with and without cross-linked VN and cultivated with A673 and PDX73 ES cell lines for two and three weeks. VN secretion to culture media was assessed using ELISA. Morphometric analysis was applied for phenotypic characterization. VN release to culture media was higher in 3D models than in monolayer cultures, and intracellular, intercellular, and pericluster presence was also observed. A673-HGs showed lower density of clusters but a proportion of larger clusters than PDX73-HGs, which presented low cluster circularity. The cluster density of A673-HGs without added VN was higher than with added VN and slightly lower in the case of PDX73-HGs. Furthermore, a culture time of three weeks provided no benefits in cluster growth compared to two weeks, especially in A673-HGs. These advances in 3D modeling and digital quantification pave the way for future studies in ES and other cancers to deepen understanding about intra- and intercellular heterogeneity and anti-adhesion VN therapies.

摘要

尤因肉瘤(ES)是一种侵袭性的儿童骨与软组织癌症。在其他癌症中,高玻连蛋白(VN)表达与预后不良相关,我们旨在确定这种细胞外基质糖蛋白作为ES侵袭性生物标志物的效用。制备了含和不含交联VN的丝素蛋白加明胶 - 酪胺水凝胶(HG),并与A673和PDX73 ES细胞系共培养两周和三周。使用酶联免疫吸附测定法评估培养基中的VN分泌。应用形态计量分析进行表型特征描述。在三维模型中,VN向培养基中的释放高于单层培养,并且还观察到细胞内、细胞间和簇周存在情况。A673 - HG显示出较低的簇密度,但比PDX73 - HG有更大比例的较大簇,而PDX73 - HG的簇圆度较低。未添加VN的A673 - HG的簇密度高于添加VN的情况,而PDX73 - HG的情况则略低。此外,与两周相比,三周的培养时间对簇生长没有益处,尤其是在A673 - HG中。三维建模和数字定量方面的这些进展为ES和其他癌症的未来研究铺平了道路,以加深对细胞内和细胞间异质性以及抗粘附VN疗法的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec7e/11476106/cb184c2224fb/cancers-16-03347-g001.jpg

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