首页> 外文期刊>International Journal of Hematology and Oncology >Angiotensin Converting Enzyme (ACE) Insertion/Deletion (I/D) Gene Polymorphisms in Leukemic Hematopoiesis
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Angiotensin Converting Enzyme (ACE) Insertion/Deletion (I/D) Gene Polymorphisms in Leukemic Hematopoiesis

机译:白血病造血过程中血管紧张素转换酶(ACE)插入/缺失(I / D)基因多态性

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Local bone marrow renin-angiotensin system (RAS) is an autocrine-paracrine system affecting normal and neoplastic hematopoiesis. Angiotensin converting enzyme (ACE) converts angiotensinogen-I to its physiologically active peptide angiotensin-II, which stimulates proliferation and differentiation of hematopoietic stem cells through angiotensin II type 1 receptors. We investigated the ACE insertion/deletion (I/D) gene polymorphisms in patients with hematological malignancies including acute and chronic leukemia, myelodysplastic syndrome and multiple myeloma. Our results showed that 80.4% of the patients represented ID/II genotype, whereas it was 55.9% of the control group and 3.2 fold increased disease risk in the existence of insertion allele (ID/II). This is the first study demonstrating possible effects of ACE I/D gene polymorphism of the local bone marrow RAS components on leukemic hematopoiesis.
机译:局部骨髓肾素-血管紧张素系统(RAS)是一种影响正常和肿瘤性造血功能的自分泌-旁分泌系统。血管紧张素转化酶(ACE)将血管紧张素原I转化为其生理活性肽血管紧张素II,该肽通过血管紧张素II 1型受体刺激造血干细胞的增殖和分化。我们调查了血液恶性肿瘤患者的ACE插入/缺失(I / D)基因多态性,包括急性和慢性白血病,骨髓增生异常综合症和多发性骨髓瘤。我们的结果表明,有80.4%的患者代表ID / II基因型,而在对照组中则为55.9%,在存在插入等位基因(ID / II)的情况下疾病风险增加了3.2倍。这是第一项证明局部骨髓RAS成分的ACE I / D基因多态性对白血病造血功能可能产生的影响的研究。

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