血清丝裂原活化蛋白激酶1与赖氨酰氧化酶样蛋白2联合检测对宫颈癌早期诊断的价值

Value of combined detection of serum mitogen-activated protein kinase 1 and lysyl oxidase-like protein 2 in early diagnosis of cervical cancer

  • 摘要:
    目的 探讨血清丝裂原活化蛋白激酶1(MAPK1)与赖氨酰氧化酶样蛋白2(LOXL2)联合检测对宫颈癌早期诊断的价值。
    方法 选取218例宫颈病变患者作为研究组(宫颈癌组103例, 良性肿瘤组115例),选取100例宫颈上皮内瘤变Ⅱ级患者作为癌前病变组,另选取同期79例健康体检者作为对照组。检测各组血清MAPK1、LOXL2水平,采用Pearson相关性分析评估宫颈癌组患者血清MAPK1水平与LOXL2水平的相关性; 通过Logistic回归分析筛选宫颈癌发生的影响因素; 绘制受试者工作特征(ROC)曲线,评估血清MAPK1和LOXL2对宫颈癌的诊断效能。
    结果 研究组血清MAPK1、LOXL2水平高于癌前病变组和对照组,且癌前病变组高于对照组,差异有统计学意义(P < 0.05); 宫颈癌组高危型人乳头瘤病毒(HPV)感染者占比和血清MAPK1、LOXL2水平均高于良性肿瘤组,差异有统计学意义(P < 0.05); Ⅲ~Ⅳ期宫颈癌患者血清MAPK1、LOXL2水平高于Ⅰ~Ⅱ期宫颈癌患者,差异有统计学意义(P < 0.05)。Pearson相关性分析结果显示,宫颈癌组患者血清MAPK1水平与LOXL2水平呈正相关(r=0.468,P < 0.001)。Logistic回归分析结果显示,高危型HPV感染、MAPK1和LOXL2均为宫颈癌发生的影响因素(P < 0.05)。ROC曲线分析显示,血清MAPK1和LOXL2联合诊断的曲线下面积(AUC)为0.911, 显著大于单独诊断的AUC(0.848和0.843)。
    结论 宫颈癌患者血清MAPK1和LOXL2水平显著上调,且二者水平呈正相关。高危型HPV感染、血清MAPK1和LOXL2水平为宫颈癌发生的影响因素,联合检测MAPK1和LOXL2水平有望辅助诊断宫颈癌。

     

    Abstract:
    Objective To explore the value of combined detection of serum mitogen-activated protein kinase 1 (MAPK1) and lysyl oxidase-like protein 2 (LOXL2) in early diagnosis of cervical cancer.
    Methods A total of 218 patients with cervical lesions were selected as study group (103 cases in cervical cancer group, 115 cases in benign tumor group). Additionally, 100 patients with cervical intraepithelial neoplasia grade Ⅱ were selected as precancerous lesion group, and 79 healthy individuals undergoing physical examinations during the same period were selected as control group. Serum levels of MAPK1 and LOXL2 were measured in each group. Pearson correlation analysis was used to evaluate the correlations of serum MAPK1 and LOXL2 levels in patients with cervical cancer. Logistic regression analysis was performed to screen influencing factors for the occurrence of cervical cancer. Receiver operating characteristic (ROC) curves were plotted to assess the diagnostic efficacy of serum MAPK1 and LOXL2 for cervical cancer.
    Results Serum MAPK1 and LOXL2 levels in the study group were higher than those in the precancerous lesion group and the control group, and those in the precancerous lesion group were higher than those in the control group, with statistically significant differences (P < 0.05). The proportion of patients with high-risk human papillomavirus (HPV) infection and serum MAPK1 and LOXL2 levels in the cervical cancer group were higher than those in the benign tumor group, with statistically significant differences (P < 0.05). Serum MAPK1 and LOXL2 levels in patients with stage Ⅲ to Ⅳ cervical cancer were higher than those in patients with stage Ⅰ to Ⅱ cervical cancer, with statistically significant differences (P < 0.05). Pearson correlation analysis showed a positive correlation between serum MAPK1 and LOXL2 levels in patients with cervical cancer (r=0.468, P < 0.001). Logistic regression analysis showed that high-risk HPV infection, MAPK1 and LOXL2 were all influencing factors for the occurrence of cervical cancer (P < 0.05). ROC curve analysis showed that the area under the curve (AUC) for combined diagnosis of serum MAPK1 and LOXL2 was 0.911, which was significantly greater than the AUCs for individual diagnoses (0.848 and 0.843, respectively).
    Conclusion Serum MAPK1 and LOXL2 levels in patients with cervical cancer are significantly upregulated, and the two indicators were positively correlated. High-risk HPV infection, serum MAPK1 and LOXL2 levels were influencing factors for the occurrence of cervical cancer. Combined detection of MAPK1 and LOXL2 levels is expected to assist in the diagnosis of cervical cancer.

     

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