Suppr超能文献

错配双链RNA对新鲜人肿瘤细胞的抗增殖作用:克隆形成试验分析

Antiproliferative effect of mismatched double-stranded RNA on fresh human tumor cells analyzed in a clonogenic assay.

作者信息

Strayer D R, Watson P, Carter W A, Brodsky I

出版信息

J Interferon Res. 1986 Aug;6(4):373-9. doi: 10.1089/jir.1986.6.373.

Abstract

Colony growth in soft agar was used to identify human tumors that were sensitive to the direct antiproliferative effects of mismatched dsRNA (Ampligen). The results suggest that different human solid malignancies vary significantly in their sensitivity to Ampligen. Tumors with 50% or more of their surgical specimens showing sensitivity included carcinoid, glioblastoma, and carcinomas of the kidney, and lung. Resistant tumors (less than 15% sensitivity) included sarcomas and colo-rectal carcinomas. Overall, 42% of the tumor specimens studied showed a 50% or greater reduction in tumor cell colony formation after a single initial treatment with Ampligen (250 micrograms/ml). Interestingly, one patient's tumor which was de novo sensitive to interferon (IFN), but emerged as IFN-resistant following IFN therapy, remained sensitive to Ampligen. Thus, a clonogenic assay may prove useful in identifying human tumors and individuals for clinical trials with Ampligen, including patients resistant to IFN.

摘要

利用软琼脂中的集落生长来鉴定对错配双链RNA(Ampligen)的直接抗增殖作用敏感的人类肿瘤。结果表明,不同的人类实体恶性肿瘤对Ampligen的敏感性差异显著。手术标本中50%或更多显示敏感的肿瘤包括类癌、胶质母细胞瘤以及肾癌和肺癌。耐药肿瘤(敏感性低于15%)包括肉瘤和结直肠癌。总体而言,在单次初始使用Ampligen(250微克/毫升)治疗后,42%的研究肿瘤标本显示肿瘤细胞集落形成减少了50%或更多。有趣的是,一名患者的肿瘤起初对干扰素(IFN)敏感,但在IFN治疗后出现耐药,而对Ampligen仍保持敏感。因此,克隆形成试验可能有助于识别适合用Ampligen进行临床试验的人类肿瘤和个体,包括对IFN耐药的患者。

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