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首页> 外文期刊>Orphanet journal of rare diseases >Improvement of genetic stability in lymphocytes from Fanconi anemia patients through the combined effect of α-lipoic acid and N-acetylcysteine
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Improvement of genetic stability in lymphocytes from Fanconi anemia patients through the combined effect of α-lipoic acid and N-acetylcysteine

机译:通过α-硫辛酸和N-乙酰半胱氨酸的联合作用改善范可尼贫血患者淋巴细胞的遗传稳定性

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Fanconi Anemia (FA) is a rare genetic disorder, characterized by progressive bone marrow failure and increased predisposition to cancer. Despite being highly heterogeneous, all FA patients are hypersensitive to alkylating agents, in particular to 1,2:3,4-diepoxybutane (DEB), and to oxidative damage. Recent studies point to defective mitochondria in FA cells, which is closely related with increased production of reactive oxygen species (ROS) and concomitant depletion of antioxidant defenses, of which glutathione is a well-known biomarker. The objective of the present work is to evaluate the putative protective effect of α-lipoic acid (α-LA), a mitochondrial protective agent, and N-acetylcysteine (NAC), a direct antioxidant and a known precursor for glutathione synthesis, in spontaneous and DEB-induced chromosome instability (CI) in lymphocyte cultures from FA patients. For that purpose, lymphocyte cultures from 15 FA patients and 24 healthy controls were pre-treated with 20?μM α-LA, 500?μM NAC and α-LA plus NAC at the same concentrations, and some of them were exposed to DEB (0.05?μg/ml). A hundred metaphases per treatment were scored to estimate the relative frequency of spontaneous and DEB-induced chromosome breakage. The obtained results revealed that a cocktail of α-LA and NAC can drastically improve the genetic stability in FA lymphocytes in vitro, decreasing CI by 60% and 80% in cultures from FA patients and FA mosaic/chimera patients, respectively. These results suggest that the studied cocktail can be used as a prophylactic approach to delay progressive clinical symptoms in FA patients caused by CI, which can culminate in the delay of the progressive bone marrow failure and early cancer development.
机译:范可尼贫血(FA)是一种罕见的遗传性疾病,其特征是进行性骨髓衰竭和易患癌症。尽管高度异质性,但所有FA患者对烷基化剂(尤其是1,2:3,4-二环氧丁烷(DEB))和氧化损伤均非常敏感。最近的研究指出FA细胞中的线粒体缺陷,这与活性氧(ROS)的产生增加和抗氧化剂防御能力的降低密切相关,其中谷胱甘肽是众所周知的生物标志物。本工作的目的是评估线粒体保护剂α-硫辛酸(α-LA)和直接抗氧化剂和已知的谷胱甘肽合成前体N-乙酰半胱氨酸(NAC)的自发保护作用FA患者淋巴细胞培养中DEB诱导的染色体不稳定性(CI)。为此,用20?μMα-LA,500?μMNAC和α-LA加NAC以相同浓度预处理15名FA患者和24名健康对照的淋巴细胞培养物,其中一些暴露于DEB( 0.05?μg/ ml)。对每个处理的一百个中期进行评分,以估计自发和DEB诱导的染色体断裂的相对频率。获得的结果表明,α-LA和NAC的混合物可以显着改善体外FA淋巴细胞的遗传稳定性,在FA患者和FA花叶/嵌合体患者的培养物中,CI分别降低60%和80%。这些结果表明,所研究的鸡尾酒可被用作预防方法,以延迟由CI引起的FA患者的进行性临床症状,最终可导致进行性骨髓衰竭和早期癌症发展的延迟。

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