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首页> 外文期刊>Gastroenterology research and practice >Circulating Oxidized Low-Density Lipoproteins and Antibodies against Oxidized Low-Density Lipoproteins as Potential Biomarkers of Colorectal Cancer
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Circulating Oxidized Low-Density Lipoproteins and Antibodies against Oxidized Low-Density Lipoproteins as Potential Biomarkers of Colorectal Cancer

机译:循环氧化低密度脂蛋白和抗氧化低密度脂蛋白的抗体作为结直肠癌的潜在生物标志物

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Introduction. The aim of the study was evaluation of the diagnostic utility of serum oxidized low-density lipoproteins (oxLDL), antibodies against oxLDLs (o-LAB), and CEA as risk markers of colorectal cancer (CRC). Material and Methods. The serum levels of study factors were measured in 73 patients with CRC and in 35 healthy controls who were gender-and BMI-matched to the study group. Concentrations of oxLDL, o-LAB, and CEA were detected in ELISA tests. Serum lipids, lipoproteins, and glucose levels were also coestimated. Results. Age and o-LAB were significant factors of CRC presence, but results of logistic regression analysis showed that both were weak predictors of CRC risk. Concentration of o-LAB was significantly higher in colon cancer than in rectal cancer, especially when the cancer was located in the right section of colon. Serum CEA levels were significantly elevated in the advanced stage of disease, primary tumor progression, angiolymphatic invasion, and presence of distant metastasis. Conclusions. Obtained results have demonstrated that oxLDL and o-LAB were not satisfactory risk markers of CRC. Although significant relation between o-LAB level and CRC is observed, it may be rather the result of individual differences in the host immune responses against cancer.
机译:介绍。该研究的目的是评估血清氧化低密度脂蛋白(OXLDL)的诊断用途(OXLDL),抗exldls(O-LAB)的抗体,以及CEA作为结肠直肠癌(CRC)的风险标志物。材料与方法。在73例CRC患者中测量了血清研究因子和35例健康对照,他们与研究组进行了性别和BMI匹配。在ELISA试验中检测到OXLDL,O-LAB和CEA的浓度。血清脂质,脂蛋白和葡萄糖水平也结束。结果。年龄和O-Lab是CRC存在的重要因素,但Logistic回归分析的结果表明,两者都是CRC风险的弱预测因子。结肠癌的O-Lab浓度显着高于直肠癌,特别是当癌症位于结肠的右侧部分时。在疾病的晚期阶段,初级肿瘤进展,血小阴酰虫侵袭和远处转移的存在下,血清CEA水平显着升高。结论。获得的结果表明,OXLDL和O-LAB的CRC的风险标记不令人满意。虽然观察到O-Lab水平和CRC之间的显着关系,但可能是宿主免疫反应对癌症的个体差异的结果。

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