GROβ 在结直肠癌肿瘤血清中的表达与临床病理相关性研究

Correlation between serum GROβ expression and clinicopathological characteristics of colorectal cancer

  • 摘要: 目的:探讨生长相关癌基因产物β(growth-related gene product β ,GRO β)用于结直肠癌诊断潜在的可能性。方法:收集123 例结直肠癌、88例健康对照及125 例非肿瘤患者外周血清,ELISA 法分析GRO β 的含量;免疫发光法分析CEA 及CA19- 9 的含量。统计分析不同临床特征结直癌之间GRO β 的差异;ROC 曲线评估GRO β 、CEA 和CA19- 9 诊断结直肠癌的敏感度和特异度。结果:结直肠癌血清GRO β 浓度(中位数96.15pg/mL)明显高于健康对照组(中位数43.28pg/mL,P < 0.01)和非肿瘤患者(中位数57.30pg/mL,P < 0.01)。 GRO β 水平与肿瘤TNM 分期(P < 0.01)及浸润深度均呈正相关(P < 0.05),与肿瘤分化程度、肿瘤栓塞、淋巴结转移、肿瘤病理类型及性别无关。GRO β 检测结直肠癌的敏感度和特异度分别为56.1%(69/ 123)和95.31%(203/ 213)。 将GRO β 、CEA 和CA19- 9 阳性样本叠加后,诊断Ⅰ期结直肠癌的敏感度为22.2%(4/ 18),诊断Ⅱ期结直肠癌的敏感度为66.7%(26/39)。 GRO β 的ROC 曲线下面积(0.834)高于CEA(0.739)和CA19- 9(0.676)。 结论:血清GRO β 浓度可能是一个有效的结直肠癌检测指标。

     

    Abstract: Objective:To confirm the potential of growth- related gene productβ (GRO β ) as a biomarker for colorectal cancer. Methods:Serum GROβ levels in 123 subjects with colorectal cancer, 88healthy controls, and 125 subjects with other diseases were measured using enzyme-linked immunosorbent assay. Serum levels of carcinoembryonic antigen (CEA) and carbohydrate antigen 19- 9 (CA 19- 9) in all subjects were measured using immunoluminometric assay. Statistical analyses were conducted to determine the associa -tions between serum GRO β levels and clinical parameters for colorectal cancer. The receiver operating characteristic (ROC) curves of GROβ , CEA, and CA 19- 9 were analyzed.Results: The serum GRO β levels were higher in patients with colorectal cancer (median= 96.15pg/mL) than in the healthy controls (median=43.28pg/mL, P<0.01) and in patients with other diseases (median= 57.30pg/mL, P< 0.01). The serum GRO β levels in patients with colorectal cancer were positively correlated with the tumor-node-metastasis staging ( P< 0.01) and depth of infiltration ( P<0.05), but not with the histological grade, tumor embolus, lymph node metastasis, gross pathologic tu-mor type, or gender of the patients. The sensitivity and specificity of the assay for serum GRO β were 56.1% (69/123) and95.31% (203/213), respectively. The diagnostic sensitivity was 22.2% (4/18) for stage I and 66.7% (26/39) for stage II when the data of GRO β were combined with the data of CEA and CA19- 9. The ROC curve constructed with the data of GRO β (0.834) was larger than that construct -ed with the data of CEA ( 0.739) or CA19- 9 (0.676) for discriminating colorectal cancer from the matched controls. Conclusion:These preliminary results indicated that the serum GRO β level could be a useful biomarker for colorectal cancer diagnoses.

     

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