国际肿瘤学杂志 ›› 2021, Vol. 48 ›› Issue (12): 735-738.doi: 10.3760/cma.j.cn371439-20201119-00145

• 论著 • 上一篇    下一篇

DNA甲基转移酶1和叉头蛋白转录因子O亚型3a在结肠癌中的表达关系研究

刘瑾1, 陈翔1, 马群1, 童东东2   

  1. 1西安国际医学中心医院肿瘤内科 710038
    2西安交通大学医学部 710038
  • 收稿日期:2020-11-19 修回日期:2021-02-26 出版日期:2021-12-08 发布日期:2022-01-12
  • 基金资助:
    国家自然科学基金(81702918)

Study on expression relationship of DNA methyltransferase 1 and forkhead box O3a in colon cancer

Liu Jin1, Chen Xiang1, Ma Qun1, Tong Dongdong2   

  1. 1Department of Oncology, Xi'an International Medical Center Hospital, Xi'an 710038, China
    2Department of Medicine, Xi'an Jiaotong University, Xi'an 710038, China
  • Received:2020-11-19 Revised:2021-02-26 Online:2021-12-08 Published:2022-01-12
  • Supported by:
    National Natural Science Foundation of China(81702918)

摘要: 目的 通过检测DNA甲基转移酶1(DNMT1)和叉头蛋白转录因子O亚型(FOXO)3a在结肠癌患者血清中的水平,分析两者在结肠癌中的关系以及联合检测预测结肠癌发生的诊断效能。 方法 选取2019年9月至2020年9月西安国际医学中心医院确诊并收治的结肠癌患者105例作为结肠癌组,65例同期经活检确诊的结肠息肉患者作为对照组。采用实时荧光定量PCR检测患者血清中DNMT1、FOXO3a水平;Pearson相关分析结肠癌患者血清中DNMT1、FOXO3a的相关性;采用受试者工作特征曲线对DNMT1、FOXO3a水平在结肠癌中的诊断价值进行评估。 结果 对照组与结肠癌组患者血清中DNMT1水平分别为0.93±0.28和1.34±0.35,与对照组相比,结肠癌组患者中DNMT1水平显著升高,差异具有统计学意义(t=7.990,P<0.001);两组患者血清中FOXO3a水平分别为1.04±0.39和0.69±0.18,与对照组相比,结肠癌组患者中FOXO3a水平降低,差异具有统计学意义(t=7.940,P<0.001)。DNMT1和FOXO3a的水平在结肠癌患者血清中呈负相关(r=-0.687,P<0.001)。DNMT1预测结肠癌发生的曲线下面积(AUC)为0.843,敏感性为71.40%,特异性为90.80%;FOXO3a预测结肠癌发生的AUC为0.812,敏感性为88.60%,特异性为67.70%;二者联合预测结肠癌发生的AUC为0.859,敏感性为89.50%,特异性为92.30%;与FOXO3a单独检测相比,二者联合检测对结肠癌的预测价值更高(Z=1.982,P=0.047)。 结论 结肠癌患者血清中DNMT1水平升高,FOXO3a水平则降低,二者在结肠癌患者血清中呈负相关,二者联合检测能够有效提高结肠癌的诊断价值。

关键词: 结肠肿瘤, DNA甲基转移酶1, 叉头蛋白转录因子O亚型3a

Abstract: Objective To analyze the relationship between DNA methyltransferase 1 (DNMT1) and forkhead box O3a (FOXO3a) in colon cancer and the diagnostic efficacy of combined detection in predicting the occurrence of colon cancer by detecting the levels of DNMT1 and FOXO3a in serum of colon cancer patients. Methods A total of 105 patients with colon cancer diagnosed and treated in Xi'an International Medical Center Hospital from September 2019 to September 2020 were selected as the colon cancer group, and 65 patients with colon polyps diagnosed by biopsy during the same period were selected as control group. The levels of DNMT1 and FOXO3a in serum of patients were detected by real-time fluorescence quantitative PCR. Pearson correlation coefficient method was used to analyze the correlation between the levels of DNMT1 and FOXO3a in serum of patients with colon cancer. Subject operating characteristic curve was used to evaluate the diagnostic values of DNMT1 and FOXO3a levels in colon cancer. Results The serum levels of DNMT1 in the control group and colon cancer group were 0.93±0.28 and 1.34±0.35, compared with the control group, the level of DNMT1 in the colon cancer group was significantly higher, with a statistically significant difference (t=7.990, P<0.001). The serum levels of FOXO3a were 1.04±0.39 and 0.69±0.18, compared with the control group, the level of FOXO3a in the colon cancer group was significantly lower, with a statistically significant difference (t=7.940, P=0.001). The serum levels of DNMT1 and FOXO3a in patients with colon cancer were negatively correlated (r=-0.687, P<0.001). The area under the curve (AUC) of DNMT1 predicting colon cancer was 0.843, the sensitivity was 71.40%, and the specificity was 90.80%. The AUC of FOXO3a predicting colon cancer was 0.812, the sensitivity was 88.60%, and the specificity was 67.70%. The AUC of the two combined predicting colon cancer was 0.859, the sensitivity was 89.50%, and the specificity was 92.30%. Compared with FOXO3a single detection, the predictive value of combined detection of DNMT1 and FOXO3a were higher (Z=1.982, P=0.047). Conclusion The level of DNMT1 in the serum of patients with colon cancer is increased, while the level of FOXO3a is decreased. There is a negative correlation between them in the serum of patients with colon cancer. The combined detection of the DNMT1 and FOXO3a can effectively improve the diagnostic value of colon cancer.

Key words: Colon neoplasms, DNA methyltransferase 1, Forkhead box O3a