文章摘要
马春芳,李翔翔,杨鸿林.血浆游离 DNA含量和完整性的动态变化在食管癌中的临床价值[J].安徽医药,2023,27(10):1986-1990.
血浆游离 DNA含量和完整性的动态变化在食管癌中的临床价值
Clinical value of dynamic changes of plasma cell free DNA content and integrity in esophageal carcinoma
  
DOI:10.3969/j.issn.1009-6469.2023.10.017
中文关键词: 食管肿瘤  血浆游离 DNA  糖类抗原 199(CA199)  癌胚抗原( CEA)  鳞状上皮细胞癌抗原( SCC)
英文关键词: Esophageal Neoplasms  Plasma cell free DNA  Carbohydrate antigen 199(CA199)  Carcinoembryonic antigen(CEA)  Squamous cell carcinoma antigen(SCC)
基金项目:苏州市第九人民医院院级科研启动基金立项( YK202226)
作者单位E-mail
马春芳 苏州市第九人民医院检验科江苏苏州 215000  
李翔翔 苏州市第九人民医院检验科江苏苏州 215000  
杨鸿林 苏州市第九人民医院检验科江苏苏州 215000 1343890567@qq.com 
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中文摘要:
      目的探讨食管癌病人血浆游离 DNA(cf-DNA)的含量和完整性(以 cf-DNA长片段 ALU247与短片段 ALU115含量的比值表示)在食管癌诊治中的临床意义。方法选择 2020年 6月至 2022年 5月苏州市第九人民医院收治的 50例食管癌病人、 50例食管良性肿瘤病人、 50例健康对照者为前瞻性研究的研究对象,分别纳入食管癌组、食管良性病变组以及健康对照组,用微量血液基因组提取试剂盒( Qiagen)提取血浆 cf-DNA,并以实时荧光定量 PCR法检测 cf-DNA含量,收集其中 25例食管癌病人术后血浆并检测 cf-DNA含量,动态监测 cf-DNA在术前术后的变化。检测食管癌病人糖类抗原 199(CA199)、癌胚抗原(CEA)、鳞状上皮细胞癌抗原( SCC)含量,比较 cf-DNA和肿瘤标志物在食管癌中的诊断价值。结果食管癌组、良性病变组、健康对照组术前食管癌血浆 ALU115含量[ 4.30(2.06,8.36)μg/L,1.98(1.38,3.02)μg/L,1.63(0.87,2.66)μg/L]; ALU247含量[1.40(0.91,4.10)μg/L,0.63(0.37,1.27)μg/L,0.26(0.15,0.43)μg/L]; cf-DNA完整性[ 0.41(0.29,0.69), 0.33(0.25,0.50), 0.18(0.11,0.28)](均 P<0.05); ALU115[术前 4.41(2.04,8.87)μg/L,术后 1.05(0.66,1.75)μg/L]以及完整性[术前 0.49(0.27,0.77)术后 0.30(0.17,0.37)]在术前术后相比差异有统计学意义( P<0.05);在食管癌分期、分化程度、是否有远处转移上血浆 cf-DNA差异有统计学意义( P<0.05);相比传统肿瘤标志物,血浆 cf-DNA的诊断效能更高,当 ALU247含量取 0.65 μg/L时,受试者操作特征(ROC)曲线下面积最大,为 0.95。结论血浆 cf-DNA检测在食管癌诊治、预后中有一定的临床价值。
英文摘要:
      Objective To investigate the clinical significance of plasma cell free DNA (cf-DNA) content and integrity in the diagnosis and treatment of esophageal cancer.Methods Fifty patients with esophageal cancer, 50 patients with benign esophageal tumors,and 50 healthy controls admitted to the Suzhou Ninth People′s Hospital from June 2020 to May 2022 were selected as study subjectsfor the prospective study, and were included in the esophageal cancer group, the group with benign esophageal lesions, and the controlgroup, respectively. A micro blood genome extraction kit (Qiagen) was used to extract cf-DNA, and real-time fluorescence quantitative PCR was utilized to evaluate the plasma cf-DNA content. The postoperative plasma of 25 esophageal cancer patients was collected, and the cf-DNA content was quantified, as well as the variations in cf-DNA before and after surgery, which were dynamically identified. Atthe same time, the levels of tumor markers carbohydrate antigen 199 (CA199), carcinoembryonic antigen (CEA) and squamous cell carcinoma antigen (SCC) were also examined in patients with esophageal cancer to compare the difference between the diagnostic significance of cf-DNA and tumor markers in esophageal cancer.Results Preoperative plasma ALU115 content in esophageal cancer [4.30(2.06, 8.36)μg/L, 1.98(1.38, 3.02)μg/L, 1.63(0.87, 2.66)μg/L]; ALU247 content [1.40(0.91, 4.10)μg/L, 0.63(0.37, 1.27)μg/L, and 0.26(0.15,0.43)μg/L]; and free DNA integrity [0.41(0.29,0.69), 0.33(0.25,0.50), 0.18(0.11, 0.28) ] in the esophageal cancer group,benign lesion group and healthy control group ,showed statistically significant differences among the three groups (P<0.05); The difference in ALU115 [preoperative 4.41 (2.04,8.87)μg/L, postoperative 1.05 (0.66,1.75)μg/L] as well as integrity [preoperative 0.49 (0.27, 0.77),postoperative 0.30 (0.17,0.37)] was statistically significant when compared before and after surgery (P<0.05); Additionally, there were statistical differences in plasma cf-DNA according to the stage, level of differentiation, and existence of distant metastases in esophageal cancer (P< 0.05). Compared with the conventional tumor markers, the diagnostic accuracy of plasma cf-DNA was greater, and the area under the ROC curve was the maximum at 0.95 when the ALU247 level was taken as 0.65μg/L.Conclusion Testing for plasma cf-DNA has certain clinical value for the diagnosis and therapy of esophageal cancer.
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