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Published in: BMC Cancer 1/2016

Open Access 01-12-2016 | Research article

Prediction of cancer progression in a group of 73 gastric cancer patients by circulating cell-free DNA

Authors: Wang-Yang Pu, Rong Zhang, Li Xiao, Yong-You Wu, Wei Gong, Xiao-Dong Lv, Feng-Yun Zhong, Zhi-Xiang Zhuang, Xu-Ming Bai, Kai Li, Chun-Gen Xing

Published in: BMC Cancer | Issue 1/2016

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Abstract

Background

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.

Methods

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.

Results

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.

Conclusions

Concentration of ccf-DNA is a promising molecular marker for assessing gastric cancer progression.

Trial registration

Current Controlled Trials ChiCTR-DDT-12002848, 8 October 2012.
Appendix
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Metadata
Title
Prediction of cancer progression in a group of 73 gastric cancer patients by circulating cell-free DNA
Authors
Wang-Yang Pu
Rong Zhang
Li Xiao
Yong-You Wu
Wei Gong
Xiao-Dong Lv
Feng-Yun Zhong
Zhi-Xiang Zhuang
Xu-Ming Bai
Kai Li
Chun-Gen Xing
Publication date
01-12-2016
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2016
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-016-2977-7

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