Suppr超能文献

重组干扰素-α和5-氟尿嘧啶对结肠癌细胞或外周血单个核细胞的不同作用。

Differential effects of recombinant interferon-alpha and 5-fluorouracil against colon cancer cells or against peripheral blood mononuclear cells.

作者信息

De Filippi R, Prete S P, Giuliani A, Silvi E, Yamaue H, Nieroda C A, Greiner J W, De Vecchis L, Bonmassar E

机构信息

Laboratory of Tumor Immunology and Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

出版信息

Anticancer Res. 1994 Sep-Oct;14(5A):1767-73.

PMID:7847809
Abstract

Comparative studies on the suppressive effects of recombinant interferon-alpha (IFN-alpha), 5-fluorouracil (5-FU), or IFN-alpha + 5-FU have been performed in vitro on colon carcinoma cells (HT-29 cell line) and PHA-stimulated mononuclear cells (MNC) of peripheral blood obtained from healthy donors. IFN-alpha was used at 500 U/ml against HT-29 cells and at 1000 U/ml against MNC on day 1 of culture; 5-FU was used at 250 microM against HT-29 and at 1400 microM against MNC on day 2 of culture. The results show that: (a) IFN-alpha inhibited MNC and HT-29 cells by 13.4% and 32.9%, respectively; (b) 5-FU inhibited MNC and HT-29 cells by 54.7% and 87.0%, respectively; (c) IFN-alpha + 5-FU resulted in a stronger inhibition of HT-29 cells (i.e., 96.1%). In contrast, that combination was significantly less suppressive than 5-FU alone when MNC were used as targets (i.e., 35.9% inhibition). Natural cell-mediated cytotoxic activity relative to 10(6) MNC was not markedly altered by all agents alone or in combination. Moreover, treatment with IFN-alpha, 5-FU or IFN-alpha + 5-FU resulted in a marked increase in the number of HT-29 cells positive for the CEA surface antigen. These data seem to provide further rational support of the clinical use of IFN-alpha + 5-FU in colorectal cancer, based on the differential toxicity of this drug combination on tumor versus normal immunocompetent cells.

摘要

已对重组干扰素-α(IFN-α)、5-氟尿嘧啶(5-FU)或IFN-α + 5-FU在体外对结肠癌细胞(HT-29细胞系)以及从健康供体获得的外周血中PHA刺激的单核细胞(MNC)的抑制作用进行了比较研究。在培养第1天,IFN-α对HT-29细胞的使用浓度为500 U/ml,对MNC的使用浓度为1000 U/ml;在培养第2天,5-FU对HT-29细胞的使用浓度为250 μM,对MNC的使用浓度为1400 μM。结果显示:(a)IFN-α分别抑制MNC和HT-29细胞13.4%和32.9%;(b)5-FU分别抑制MNC和HT-29细胞54.7%和87.0%;(c)IFN-α + 5-FU对HT-29细胞产生更强的抑制作用(即96.1%)。相比之下,当以MNC作为靶细胞时,该组合的抑制作用明显低于单独使用5-FU(即35.9%的抑制率)。相对于10⁶ MNC的天然细胞介导的细胞毒性活性,单独或联合使用所有药物均未发生明显改变。此外,用IFN-α、5-FU或IFN-α + 5-FU处理导致CEA表面抗原阳性的HT-29细胞数量显著增加。基于该药物组合对肿瘤细胞与正常免疫活性细胞的不同毒性,这些数据似乎为IFN-α + 5-FU在结直肠癌临床应用中提供了进一步的合理依据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验