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本文引用的文献

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Possible requirement of internalization in the mechanism of in vitro cytotoxicity in tumor necrosis serum.肿瘤坏死血清体外细胞毒性机制中内化作用的可能需求。
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Effect of recombinant human tumor necrosis factor on human nasopharyngeal carcinoma cell line in vitro.重组人肿瘤坏死因子对人鼻咽癌细胞系的体外作用。
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Augmentation of cytotoxic activity of recombinant human tumor necrosis factor (rHu-TNF) by recombinant human interferon-gamma (rHu-IFN-gamma).重组人干扰素-γ(rHu-IFN-γ)增强重组人肿瘤坏死因子(rHu-TNF)的细胞毒活性。
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人重组肿瘤坏死因子α与微管效应物联合的协同细胞毒性

Synergistic cytotoxicity of human recombinant tumour necrosis factor alpha combined with microtubule effectors.

作者信息

Baumgart J, Schlott B, Suehnel J, Vater W, Schulze W, Behnke D

机构信息

Institute of Microbiology and Experimental Therapy, Jena, Federal Republic of Germany.

出版信息

J Cancer Res Clin Oncol. 1991;117(3):239-43. doi: 10.1007/BF01625431.

DOI:10.1007/BF01625431
PMID:2033091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12201880/
Abstract

Combinations of human recombinant tumour necrosis factor alpha (rhTNF alpha) with each of four different agents disturbing the microtubule system of the cellular cytoskeleton were tested for synergistic cytotoxic action against murine melanoma B16K and L-M(S) cells. In addition to the known microtubule effectors colchicine, vincristine, and taxol, the influence of the fluorenone-azo-methine derivative alpha-diphenylene-N-(p-[bis-(beta-hydroxyethyl-amino]-phenyl)- nitrone (DHPN) on the rhTNF alpha cytotoxicity was studied. Applying a novel computer-based isobole method [Suehnel J (1990) Antiviral Res 13:23-40] concentration ranges of synergistic, zero, and antagonistic interaction were found after in vitro combination of rhTNF alpha with each of the drugs tested in a 72-h cytotoxicity assay. In contrast, a 24-h exposure of B16K cells to these combinations still did not inhibit in vitro colony formation to a greater extent than either drug alone. A preliminary in vivo experiment revealed an increased antitumour effect after treatment of established subcutaneous melanoma B16 tumours with a combination of rhTNF alpha and DHPN.

摘要

研究了重组人肿瘤坏死因子α(rhTNFα)与四种不同的破坏细胞骨架微管系统的药物联合使用时,对小鼠黑色素瘤B16K和L-M(S)细胞的协同细胞毒性作用。除了已知的微管效应物秋水仙碱、长春新碱和紫杉醇外,还研究了芴酮-偶氮-甲碱衍生物α-二亚苯基-N-(对-[双-(β-羟乙基-氨基]-苯基)-硝酮(DHPN)对rhTNFα细胞毒性的影响。应用一种新型的基于计算机的等效线法[Suehnel J(1990)Antiviral Res 13:23-40],在72小时细胞毒性试验中,rhTNFα与每种受试药物体外联合后,发现了协同、无作用和拮抗相互作用的浓度范围。相比之下,B16K细胞在24小时内暴露于这些联合药物中,对体外集落形成的抑制程度仍不大于单独使用任何一种药物。一项初步的体内实验表明,用rhTNFα和DHPN联合治疗已建立的皮下黑色素瘤B16肿瘤后,抗肿瘤效果增强。