Boorman G A, Luster M I, Dean J H, Campbell M L
Environ Health Perspect. 1982 Feb;43:129-35. doi: 10.1289/ehp.8243129.
Potential antineoplastic agents must be screened for the delayed toxicity that occurs in many cases of drug-induced bone marrow aplasia. In vitro clonal assays for hematopoietic progenitor cells have been developed to assess the degree of myelotoxicity. This adverse side effect is often the limiting factor in the development of new cancer chemotherapeutics. In addition, many environmental chemicals are cytotoxic to rapidly proliferating cells, but a systematic assessment of their myelotoxicity has not been performed. We have used clonal marrow assays to investigate a panel of chemicals including 2,3,7,8-tetrachlorodibenzo-p-dioxin, polybrominated biphenyls, diethylstilbestrol, benzo(a)pyrene and indomethacin. All were immunotoxic, some to pleuripotent hemopoetic stem cells and other to granulocyte-macrophage progenitors, and at concentrations below those causing other toxic manifestations. This shows that these bone marrow clonal assays, and hopefully future one for erythroid, B- and T-lymphocytes, and megakaryocytes, will provide the specificity and sensitivity necessary to delineate the myelotoxicity of a broad spectrum of environmental chemicals.
必须对潜在的抗肿瘤药物进行筛查,以检测在许多药物诱导的骨髓再生障碍病例中出现的延迟毒性。已经开发出用于造血祖细胞的体外克隆测定法,以评估骨髓毒性的程度。这种不良副作用往往是新型癌症化疗药物研发中的限制因素。此外,许多环境化学物质对快速增殖的细胞具有细胞毒性,但尚未对其骨髓毒性进行系统评估。我们已使用克隆骨髓测定法来研究一组化学物质,包括2,3,7,8-四氯二苯并对二恶英、多溴联苯、己烯雌酚、苯并(a)芘和吲哚美辛。所有这些物质都具有免疫毒性,有些作用于多能造血干细胞,有些作用于粒细胞-巨噬细胞祖细胞,且浓度低于引起其他毒性表现的浓度。这表明这些骨髓克隆测定法,以及有望在未来用于红系细胞、B淋巴细胞、T淋巴细胞和巨核细胞的测定法,将提供必要的特异性和敏感性,以描绘广泛环境化学物质的骨髓毒性。