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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:循环氧化的低密度脂蛋白和抗氧化的低密度脂蛋白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的低密度脂蛋白(oxLDL),抗oxLDLs的抗体(o-LAB)和CEA作为结直肠癌(CRC)危险标志物的诊断效用。材料和方法。在73名CRC患者和35名与研究组性别和BMI匹配的健康对照组中测量了研究因素的血清水平。在ELISA测试中检测到oxLDL,o-LAB和CEA的浓度。还对血清脂质,脂蛋白和葡萄糖水平进行了评估。年龄和o-LAB是CRC发生的重要因素,但Logistic回归分析的结果表明,两者都是CRC风险的弱预测指标。结肠癌中o-LAB的浓度显着高于直肠癌,尤其是当癌症位于结肠的右侧部分时。在疾病晚期,原发性肿瘤进展,血管淋巴管浸润和远处转移的存在下,血清CEA水平显着升高。获得的结果表明,oxLDL和o-LAB不是令人满意的CRC危险标志物。尽管观察到了o-LAB水平与CRC之间的显着关系,但这可能是宿主针对癌症的免疫反应中个体差异的结果。

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