骨髓增殖性肿瘤患者蛋白酪氨酸磷酸酶1B基因突变分析 |
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引用本文: | 周莉莉,傅建非,吴昊,李冰,梁爱斌. 骨髓增殖性肿瘤患者蛋白酪氨酸磷酸酶1B基因突变分析[J]. 白血病.淋巴瘤, 2015, 0(7): 424-427. DOI: 10.3760/cma.j.issn.1009-9921.2015.07.011 |
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作者姓名: | 周莉莉 傅建非 吴昊 李冰 梁爱斌 |
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作者单位: | 同济大学附属同济医院血液科, 上海,200065 |
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基金项目: | 国家自然科学基金(81100343) |
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摘 要: | 目的 分析骨髓增殖性肿瘤(MPN)患者中蛋白酪氨酸磷酸酶1B(PTP1B)基因突变情况.方法 采用DNA测序技术检测84例MPN患者及37例健康对照者PTP1B的DNA序列.结果 MPN患者及健康对照者均未检测到Exon1 ~6、Exon9和Exon10突变.MPN患者中有18例检测到Exon8 C/T杂合性突变,健康对照者中有10例检测到C/T杂合性突变,两组之间差异无统计学意义(x 2=0.453,P=0.501).38例患者进行了Exon7基因测序,2例有C/T杂合性突变,健康对照者中有1例G/C杂合性突变.所有受试者均未检测到纯合性突变.结论 MPN患者PTP1B基因突变与健康对照者相比没有明显差异.
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关 键 词: | 骨髓增殖性肿瘤 蛋白酪氨酸磷酸酶1B DNA测序 |
Analysis of protein tyrosine phosphatase 1B gene mutation in myeloproliferative neoplasms |
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Abstract: | Objective To analyse protein tyrosine phosphatase 1B (PTP1B) gene mutation in myeloproliferative neoplasms (MPN).Methods DNA sequencing technology was used to detect DNA sequences of PTP1B in MPN patients (n =84) and normal controls (n =37).Results For Exon1-6,Exon9 and Exon10,84 cases of MPN patients and 37 cases of control group were not detected mutation.For EXON 8,18 of 84 MPN patients had Exon8 C/T heterozygous mutation and 10 of 37 normal controls were detected C/T heterozygous mutation.There was no significant difference between MPN patients and normal controls (x2 =0.453,P =0.501).Exon7 was detected in 38 MPN patients and 2 cases of patients were found C/T heterozygous mutation,while in the control group,1 case with G/C heterozygous mutation.All of the cases were not detected homozygous mutation.Conclusion Using DNA sequencing technology to detect gene mutations of PTP1B,there is no significant difference between MPN patients and normal controls. |
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Keywords: | Myeloproliferative neoplasms Protein tyrosine phosphatase 1B DNA sequencing |
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