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化疗药物对血小板与转移性肿瘤细胞-内皮细胞相互作用的影响,以此作为评估血管内皮完整性的模型。

Effects of chemotherapeutic drugs on platelet and metastatic tumor cell-endothelial cell interactions as a model for assessing vascular endothelial integrity.

作者信息

Nicolson G L, Custead S E

出版信息

Cancer Res. 1985 Jan;45(1):331-6.

PMID:3965142
Abstract

An in vitro assay for examining the sublethal effects of chemotherapeutic agents on vascular endothelial integrity is described. Using vascular endothelial cell monolayers, the kinetics of binding of radiolabeled platelets or metastatic tumor cells were altered when endothelial cells were pretreated for 2 hr with low, clinically relevant concentrations of certain drugs. Electron microscopic examination by scanning electron microscopy revealed that these same drugs caused endothelial cell retraction and exposure of subendothelial matrix. Platelets and tumor cells were found bound only to the exposed areas of subendothelial matrix. Some drugs (bleomycin, 1,3-bis(2-chloroethyl)-1-nitrosourea, vincristine) induced rapid endothelial cell retraction and increased platelet and tumor cell binding to exposed subendothelial matrix, while one of the drugs tested (Adriamycin) caused delayed (1 to 3 days after a 2-hr drug treatment) endothelial cell retraction and increased cell binding. Of the drugs tested, only 5'-fluoro-2'-deoxyuridine which interferes with DNA replication failed to induce endothelial cell retraction and increased tumor cell and platelet binding. The results suggest that certain drug effects on the vascular endothelium can be assessed using the vascular endothelial cell monolayer model.

摘要

本文描述了一种用于检测化疗药物对血管内皮完整性亚致死效应的体外试验。使用血管内皮细胞单层,当内皮细胞用低的、临床相关浓度的某些药物预处理2小时后,放射性标记血小板或转移性肿瘤细胞的结合动力学发生了改变。通过扫描电子显微镜进行的电子显微镜检查显示,这些相同的药物导致内皮细胞收缩和内皮下基质暴露。发现血小板和肿瘤细胞仅与内皮下基质的暴露区域结合。一些药物(博来霉素、1,3-双(2-氯乙基)-1-亚硝基脲、长春新碱)诱导内皮细胞快速收缩,并增加血小板和肿瘤细胞与暴露的内皮下基质的结合,而所测试的一种药物(阿霉素)导致延迟(药物处理2小时后1至3天)内皮细胞收缩并增加细胞结合。在所测试的药物中,只有干扰DNA复制的5'-氟-2'-脱氧尿苷未能诱导内皮细胞收缩以及增加肿瘤细胞和血小板结合。结果表明,使用血管内皮细胞单层模型可以评估某些药物对血管内皮的作用。

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