Pu Wang-Yang, Zhang Rong, Xiao Li, Wu Yong-You, Gong Wei, Lv Xiao-Dong, Zhong Feng-Yun, Zhuang Zhi-Xiang, Bai Xu-Ming, Li Kai, Xing Chun-Gen
Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, China.
Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, China.
BMC Cancer. 2016 Dec 9;16(1):943. doi: 10.1186/s12885-016-2977-7.
Circulating cell-free DNA (ccf-DNA) in plasma may contain both specific and non-specific of tumor markers. The concentration and integrity of ccf-DNA may be clinical useful for detecting and predicting cancer progression.
Plasma samples from 40 healthy controls and 73 patients with gastric cancers (two stage 0, 17 stage I, 11 stage II, 33 stage III, and 10 stage IV according to American Joint Committee on Cancer stage) were assessed respectively. qPCR targeting the Alu repeats was performed using two different sets of primers amplifying the long and short segments. DNA integrity was calculated as a ratio of the long to the short fragments of Alu repeats.
Plasma DNA concentration was significantly higher in patients with stage III and IV gastric cancers than in healthy controls (p = 0.028 and 0.029 respectively). The receiver operating characteristic (ROC) curve for discriminating patients with stage III and IV gastric cancers from healthy controls had an area under the curve (AUC) of 0.744 (95% CI, 0.64 to 0.85). Circulating cell-free DNA concentration increased within 21 days following surgery and dropped by 3 months after surgery.
Concentration of ccf-DNA is a promising molecular marker for assessing gastric cancer progression.
Current Controlled Trials ChiCTR-DDT-12002848 , 8 October 2012.
血浆中的循环游离DNA(ccf-DNA)可能包含肿瘤标志物的特异性和非特异性成分。ccf-DNA的浓度和完整性在检测和预测癌症进展方面可能具有临床应用价值。
分别评估了40名健康对照者和73名胃癌患者(根据美国癌症联合委员会分期,2例0期、17例I期、11例II期、33例III期和10例IV期)的血浆样本。使用两组不同的引物对Alu重复序列进行qPCR,分别扩增长片段和短片段。DNA完整性以Alu重复序列长片段与短片段的比值计算。
III期和IV期胃癌患者的血浆DNA浓度显著高于健康对照者(分别为p = 0.028和0.029)。区分III期和IV期胃癌患者与健康对照者的受试者工作特征(ROC)曲线下面积(AUC)为0.744(95%CI,0.64至0.85)。循环游离DNA浓度在手术后21天内升高,术后3个月下降。
ccf-DNA浓度是评估胃癌进展的一个有前景的分子标志物。
当前受控试验ChiCTR-DDT-12002848,2012年10月8日。