Cervenka J, Arthur D, Yasis C
Pediatrics. 1981 Jan;67(1):119-27.
A cytogenetic test was developed to enable the diagnostic differentiation between Fanconi anemia and the group of disorders classified as "idiopathic" aplastic anemia. The method is based on the effect of the bifunctional alkylating agent mitomycin C (MMC) on chromosomes of peripheral lymphocytes in culture 92 to 96 hours. At the highest concentration of 80 ng/ml of MMC, about a 50-fold increase of chromosomal breaks and a 200-fold increase of radial figures was observed in Fanconi anemia lymphocytes in comparison with the average values for aplastic anemia cells or cells of healthy control subjects. In addition, sister chromatoid exchange analysis of cells treated with MMC demonstrated a marked inhibition of mitotic activity of lymphocytes of patients with increased sensitivity to MMC. It is advocated that the MMC-stress test should be used in each case of pancytopenia, as part of the therapy planning. The cytoreduction regimens used prior to bone marrow transplantation may produce lethal complications in patients with high clastogenic response to MMC.
一种细胞遗传学检测方法被开发出来,用于鉴别范可尼贫血与归类为“特发性”再生障碍性贫血的一组疾病。该方法基于双功能烷化剂丝裂霉素C(MMC)对培养92至96小时的外周淋巴细胞染色体的作用。在MMC浓度最高达80 ng/ml时,与再生障碍性贫血细胞或健康对照受试者的细胞平均值相比,范可尼贫血淋巴细胞中染色体断裂增加约50倍,辐射状图形增加200倍。此外,对用MMC处理的细胞进行姐妹染色单体交换分析表明,对MMC敏感性增加的患者淋巴细胞的有丝分裂活性受到明显抑制。建议在全血细胞减少的每一例病例中,将MMC应激试验作为治疗计划的一部分加以应用。骨髓移植前使用的细胞减少方案可能会在对MMC具有高致断裂反应的患者中产生致命并发症。