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在人体组织原代培养中,依他尼酸增强蒽环类药物和烷化剂的细胞毒性。

Enhancement of anthracycline and alkylator cytotoxicity by ethacrynic acid in primary cultures of human tissues.

作者信息

Nagourney R A, Messenger J C, Kern D H, Weisenthal L M

机构信息

Oncotech Inc., Irvine CA 92714.

出版信息

Cancer Chemother Pharmacol. 1990;26(5):318-22. doi: 10.1007/BF02897285.

Abstract

Ethacrynic acid [2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxyl] acetic acid, is a water-soluble diuretic agent that has been shown to potentiate the in vitro cytotoxicity of chemotherapeutic agents in established cell lines. We used the differential staining cytotoxicity (DiSC) assay to determine whether ethacrynic acid at 1 and 3.3 microM would potentiate the cytotoxicity of nitrogen mustard and/or doxorubicin in primary cultures of hematologic neoplasms from heavily pretreated patients and in normal peripheral blood lymphocytes. At 3.3 microM, ethacrynic acid was toxic to 8 of 24 (33%) tumor specimens studied. In subsequent studies, ethacrynic acid at 1 microM was toxic to only 2 of 54 (4%) tumor specimens. Significant enhancement for doxorubicin or nitrogen mustard was confined to lymphatic malignancies and to normal peripheral blood lymphocytes. Interspecimen variability was observed, with no enhancement in most individual specimens, 2-fold enhancement in some specimens, and 4-fold enhancement in occasional specimens. Clinical trials will be required to determine whether the observed in vitro activity for ethacrynic acid is associated with clinical benefit in unselected or assay-selected patients.

摘要

依他尼酸[2,3 - 二氯 - 4 - (2 - 亚甲基 - 1 - 氧代丁基)苯氧基]乙酸,是一种水溶性利尿剂,已被证明能增强化疗药物在已建立细胞系中的体外细胞毒性。我们使用差异染色细胞毒性(DiSC)测定法,来确定1微摩尔和3.3微摩尔的依他尼酸是否会增强氮芥和/或阿霉素对经过大量预处理患者的血液肿瘤原代培养物以及正常外周血淋巴细胞的细胞毒性。在3.3微摩尔时,依他尼酸对所研究的24个肿瘤标本中的8个(33%)有毒性。在后续研究中,1微摩尔的依他尼酸仅对54个肿瘤标本中的2个(4%)有毒性。阿霉素或氮芥的显著增强仅限于淋巴系统恶性肿瘤和正常外周血淋巴细胞。观察到不同标本间存在差异,大多数个体标本无增强,一些标本增强2倍,偶尔有标本增强4倍。需要进行临床试验来确定依他尼酸在体外观察到的活性是否与未选择或经测定选择的患者的临床获益相关。

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