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An Analysis of Polymorphism Lymphotoxin Alpha +252 A>G in South Indian Breast Cancer Patients

机译:南印度裔乳腺癌患者Lymphotoxin Alpha +252 A> G多态性分析

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Cytokine tumor necrosis factor contributes to a wide range of functions like inflammation, immunomodulatory and apoptotic activities. Our aim was to investigate the association of plasma levels of lymphotoxin alpha (LTA) with polymorphism rs909253 at +252A>G in primary invasive breast cancer(BC) patients. A total of 146 patients and 150 age matched healthy controls were included in the study. Genotyping was carried out by polymerase chain reaction and restriction fragment length polymorphism. Plasma levels were estimated by The MILLIPLEX? MAP Human Cytokine / Chemokine Panel magnetic bead kits. Data was statistically analysed by R software version 3.3.1. Plasma levels of LTA was significantly increased in cases when compared to controls. However, when levels was analyzed according to polymorphic subtypes there was no significant difference. The polymorphism was in consistent with the Hardy Weinberg(HW) equilibrium, showing X2 values of 2.3 (p= 0.13) and 2.02(p= 0.15) for cases and controls respectively. Odds ratio (OR) indicated that polymorphism was not significantly associated with breast cancer. Plasma levels of LTA were not altered due to polymorphism in patients and controls. Tumors of high- grade and hormone receptor negative cases showed higher frequency of the G allele, indicating that G allele patients may have worse prognosis. This study suggests that LTA +252A>G gene polymorphism is not a prominent risk factor for BC.
机译:细胞因子肿瘤坏死因子有助于多种功能,例如炎症,免疫调节和凋亡活性。我们的目的是研究原发性浸润性乳腺癌(BC)患者的血浆淋巴细胞毒素α(LTA)水平与多态性rs909253在+ 252A> G的相关性。该研究总共包括146位患者和150位年龄相匹配的健康对照组。通过聚合酶链反应和限制性片段长度多态性进行基因分型。血浆水平由The MILLIPLEX? MAP人细胞因子/趋化因子面板磁珠试剂盒。使用R软件3.3.1版对数据进行统计分析。与对照组相比,LTA的血浆水平显着增加。但是,当根据多态性亚型分析水平时,没有显着差异。多态性与Hardy Weinberg(HW)平衡相一致,病例和对照的X2值分别为2.3(p = 0.13)和2.02(p = 0.15)。几率(OR)表明多态性与乳腺癌没有显着相关性。由于患者和对照组的多态性,血浆LTA水平没有改变。高级别和激素受体阴性病例的肿瘤显示较高的G等位基因频率,表明G等位基因患者的预后可能较差。这项研究表明,LTA + 252A> G基因多态性不是BC的主要危险因素。

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