在真性红细胞增多症聚集区历史上发现的环境毒素及其诱导DNA损伤的潜力。

E A Irvin-Barnwell, K M Benson, M Lu, A Ragin, J Wheeler, R Hoffman
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引用次数: 2

摘要

2006年,有毒物质和疾病登记处收到一份请求,以确定在宾夕法尼亚州东北部的一个社区是否存在真性红细胞增多症患者群。在几个危险废物场址附近的三个县的连接处发现了大量PV病例。目前的研究评估了先前在群集区域检测到的选定数量的环境污染物诱导DNA损伤的可能性,使用造血干细胞衍生祖细胞进行体外测定。从正常脐带血中分离CD34+细胞,培养48 ~ 72小时生成红细胞祖细胞。选择了18种化合物进行测定;三氧化二砷、苯并(a)芘、苯、二氯甲烷、2,3,7,8-四氯二苯并对二恶英(TCDD)、三氯乙烯、氯化钾、乙苯、苯并[k]氟蒽、苯乙烯、氯化镉、对苯二酚、1,1,1-三氯乙烷、氰化钠、氯化锰、氧化铬、氧化铅和亚砷酸钠。化合物的遗传毒性通过彗星试验确定,毒性通过细胞活力试验确定。使用彗星试验,16种化合物在10 nM浓度下,与对照组相比,诱导了大量的DNA损伤。当评估是否存在剂量依赖关系时,18种化合物中的17种随着暴露浓度的增加导致更大的DNA损伤。2,3,7,8- tcdd的作用特别强,在1 μM下几乎可以诱导所有细胞的DNA损伤。总之,使用彗星试验评估的大多数毒素显示出诱导造血细胞DNA损伤的潜力,并且遗传毒性作用是剂量依赖性的。
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Environmental Toxins Found Historically in the Polycythemia Vera Cluster Area and their Potential for Inducing DNA Damage.

In 2006, the Agency for Toxic Substances and Disease Registry received a request to determine whether a cluster of polycythemia vera patients existed in a northeast Pennsylvania community. A significant cluster of PV cases was identified at the nexus of three counties near several hazardous waste sites. The current study evaluated the potential for a select number of environmental contaminants previously detected in the cluster area to induce DNA damage using in vitro assays with hematopoietic stem-cell derived progenitor cells. CD34+ cells were isolated from normal cord blood samples and were cultured for 48-72 hours to generate erythroid progenitor cells. Eighteen compounds were chosen for the assay; arsenic trioxide, benzo(a)pyrene, benzene, methylene chloride, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), trichloroethylene, potassium chloride, ethylbenzene, benzo[k]fluoranthene, styrene, cadmium chloride, hydroquinone, 1,1,1-trichloroethane, sodium cyanide, manganese chloride, chromium oxide, lead oxide, and sodium arsenite. Genotoxicity of the compounds was determined using the comet assay, and toxicity determined via the cell viability assay. Using the comet assay, 16 compounds at 10 nM concentration, induced a significant amount of DNA damage compared to the control. When evaluating whether a dose-dependent relationship was present, seventeen of the eighteen compounds led to greater DNA damage with increasing exposure concentrations. 2,3,7,8-TCDD was particularly potent, inducing DNA damage in virtually all cells at 1 μM. In conclusion, most of the toxins evaluated using the comet assay showed potential to induce DNA damage in hematopoietic cells, and the genotoxic effects were dose-dependent.

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