首页> 美国卫生研究院文献>Indian Journal of Hematology Blood Transfusion >Lack of Correlation Between the CCR5-Δ32 Mutation and Acute Myeloid Leukemia in Iranian Patients
【2h】

Lack of Correlation Between the CCR5-Δ32 Mutation and Acute Myeloid Leukemia in Iranian Patients

机译:伊朗患者CCR5-Δ32突变与急性髓细胞性白血病之间缺乏相关性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Chemokines and their receptors are crucially important in the pathogenesis of acute myeloblastic leukemia (AML). The CC chemokine receptor 5 (CCR5) is a specific chemokine receptor for CC chemokine ligand 3 (CCL3), CCL4 and CCL5 which all play key roles in identifying cancer properties and localization of leukemia cells. It has been demonstrated that the known mutation in CCR5 gene (CCR5-Δ32) leads to mal-expression of the receptor and affect its function. The aim of this study was to determine the rate of CCR5-Δ32 mutation within Iranian AML patients. In this study, blood samples were obtained from 60 AML patients and 300 healthy controls. The CCR5-Δ32 mutation was evaluated using Gap-PCR technique. Our results showed that CCR5-Δ32 mutation was not found in the patients, while three out of the controls had hetrozygotic form of this mutation. The rest of studied samples had the wild form of the gene. According to these findings, it can probably be concluded that the CCR5-Δ32 is not associated with susceptibility to AML in Iranian patients.
机译:趋化因子及其受体在急性粒细胞性白血病(AML)的发病机理中至关重要。 CC趋化因子受体5(CCR5)是CC趋化因子配体3(CCL3),CCL4和CCL5的特异性趋化因子受体,它们均在识别癌症特性和白血病细胞定位中起关键作用。已经证明CCR5基因(CCR5-Δ32)中的已知突变导致受体的异常表达并影响其功能。这项研究的目的是确定伊朗AML患者中CCR5-Δ32突变的发生率。在这项研究中,从60名AML患者和300名健康对照中获得了血液样本。使用Gap-PCR技术评估CCR5-Δ32突变。我们的结果表明,在患者中未发现CCR5-Δ32突变,而对照组中有3个具有这种突变的杂合子形式。其余的研究样品具有野生型基因。根据这些发现,可以得出结论,CCR5-Δ32与伊朗患者对AML的易感性无关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号