Suppr超能文献

人肿瘤体外克隆形成的化学敏感性。南加州大学 - 洛杉矶县医疗中心的经验。

Chemosensitivity of human neoplasms with in vitro clone formation. Experience at the University of Southern California - Los Angeles County Medical Center.

作者信息

Daniels J R, Daniels A M, Luck E E, Whitman B, Casagrande J T, Skinner D G

出版信息

Cancer Chemother Pharmacol. 1981;6(3):245-51. doi: 10.1007/BF00256977.

Abstract

We analyze experience with 600 specimens for in vitro chemosensitivity assessment of human neoplasms utilizing a soft agar colony-forming technique. Good test reproducibility is demonstrated. Disaggregation with collagenase enhances yield and does not alter chemosensitivity profiles. Therapeutic exposure to chemotherapy prior to biopsy reduces in vitro sensitivity to the specific agents used in vitro. The cyclophosphamide derivatives 4-hydroperoxycyclo phosphamide (4-HC) and phosphoramide mustard are active in vitro, and produce comparable rank order sensitivities among tested tumors. There is marked reduction of in vitro 4-HC sensitivity in patients with prior therapeutic cyclophosphamide exposure, supporting the use of this derivative in test systems. Rank order of test results among specimens is compared at 0.1 microgram and 10 microgram drug/ml. Substantial differences in rank order at these two dose levels are demonstrated, indicating that the in vitro test dose selected is an important variable.

摘要

我们利用软琼脂集落形成技术分析了600份人类肿瘤标本的体外化学敏感性,以进行体外化学敏感性评估。结果表明该测试具有良好的可重复性。用胶原酶解离可提高产量且不改变化学敏感性谱。活检前接受化疗会降低对体外使用的特定药物的体外敏感性。环磷酰胺衍生物4-氢过氧环磷酰胺(4-HC)和磷酰胺芥在体外具有活性,并且在测试的肿瘤中产生相当的敏感性排序。先前接受环磷酰胺治疗的患者体外4-HC敏感性明显降低,这支持了该衍生物在测试系统中的应用。比较了药物浓度为0.1微克/毫升和10微克/毫升时标本之间测试结果的排序。结果表明这两个剂量水平下的排序存在显著差异,表明所选的体外测试剂量是一个重要变量。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验