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环磷酰胺在无外源性代谢活化情况下对范科尼贫血淋巴细胞的致断裂性

Clastogenicity of cyclophosphamide in Fanconi's anemia lymphocytes without exogenous metabolic activation.

作者信息

Joenje H, Oostra A B

出版信息

Cancer Genet Cytogenet. 1986 Aug;22(4):339-45. doi: 10.1016/0165-4608(86)90026-9.

Abstract

The indirect mutagen cyclophosphamide (CP) is known to induce chromosomal aberrations in human lymphocyte cultures only after exogenous metabolic activation. We document here that lymphocytes from five patients with Fanconi's anemia (FA) exhibited extensive chromosomal breakage when cultured in the continuous presence of 1 mM CP without deliberate activation of the drug, whereas, cultures from healthy subjects were not significantly susceptible to breakage under these conditions. CP exposure also enhanced the frequency of sister chromatid exchanges (SCE), but to similar extents in control and FA subjects, suggesting that there is a similar low level of CP metabolism in FA and normal lymphocytes. The direct clastogenic effect of nonactivated CP as demonstrated here in FA lymphocyte cultures may be of value in screening for possible hypersensitivity in patients considered for CP therapy.

摘要

间接诱变剂环磷酰胺(CP)已知仅在外源代谢激活后才会在人淋巴细胞培养物中诱导染色体畸变。我们在此记录到,五名范可尼贫血(FA)患者的淋巴细胞在持续存在1 mM CP且未特意激活该药物的情况下培养时,出现了广泛的染色体断裂,而在这些条件下,健康受试者的培养物对断裂并不敏感。CP暴露还增加了姐妹染色单体交换(SCE)的频率,但在对照组和FA受试者中增加的程度相似,这表明FA淋巴细胞和正常淋巴细胞中CP代谢水平相似。如在此FA淋巴细胞培养物中所证明的,未激活的CP的直接致断裂作用可能对筛查考虑接受CP治疗的患者的可能超敏反应有价值。

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