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烷化抗肿瘤药物福嘌呤在体内和体外诱导人淋巴细胞产生的细胞遗传学损伤的持续性。

Persistence of cytogenetic damage induced by alkylating antineoplastic drug phopurinum in human lymphocytes in vivo and in vitro.

作者信息

Lazutka J R, Slapsyte G

机构信息

Ecological Genetics Laboratory, Vilnius University, Lithuania.

出版信息

Cancer Lett. 1990 Nov 5;54(3):113-8. doi: 10.1016/0304-3835(90)90031-r.

Abstract

Sister chromatid exchanges (SCEs) and structural chromosome aberrations (CAs) induced by cytostatic drug phopurinum in vivo and in vitro were studied in human lymphocytes. Phopurinum was found to cause a significant increase of CAs in lymphocytes of patients undergoing cytostatic therapy. Increased CA rates, however, declined rapidly after the cessation of treatment. This decline observed in vivo is in agreement with experimental results obtained in vitro, where it is found that the induction of SCEs and CAs occur only during the 1st cell cycle after pulse-treatment as G1 stage with phopurinum. Thus, phopurinum induced short-lived DNA damage both experimentally and in vivo.

摘要

在人类淋巴细胞中研究了细胞抑制药物磷嘌呤在体内和体外诱导的姐妹染色单体交换(SCE)和染色体结构畸变(CA)。发现磷嘌呤可使接受细胞抑制治疗患者的淋巴细胞中的CA显著增加。然而,治疗停止后,升高的CA率迅速下降。体内观察到的这种下降与体外实验结果一致,在体外实验中发现,SCE和CA仅在磷嘌呤脉冲处理后的第1个细胞周期(作为G1期)发生诱导。因此,磷嘌呤在实验和体内均诱导短暂的DNA损伤。

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