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MYC quantitation in cell-free plasma DNA by real-time PCR for gastric cancer diagnosis

Cited 27 time in Web of Science Cited 27 time in Scopus
Authors

Park, Kyoung Un; Lee, Hee Eun; Park, Do Joong; Jung, Eun Ji; Kim, Hyung-Ho; Kim, Woo Ho; Lee, Hye Seung; Choe, Gheeyoung; Song, Junghan

Issue Date
2009-05
Publisher
WALTER DE GRUYTER & CO
Citation
CLINICAL CHEMISTRY AND LABORATORY MEDICINE; Vol.47 5; 530-536
Keywords
MYCplasma DNAstomach cancerreal-time PCR
Abstract
Background: Detection of tumor-associated genetic alterations in plasma of cancer patients has recently been suggested to be an accurate method for detecting early or recurrent cancer. Methods: We performed quantitative real-time PCR for MYC and GAPDH in tissue and plasma samples of 57 patients with gastric cancer and in plasma of 79 cancer-free individuals. We also performed two-color MYC fluorescence in situ hybridization (FISH) in tissue from the 57 patients with gastric cancer. Results: The tissue MYC/GAPDH ratio by real-time PCR was significantly correlated with MYC status by FISH (p<0.001). The mean ratio of plasma MYC/GAPDH was 5.226+/-3.578 (range: 1.25-18.35) in gastric cancer patients, and 2.436+/-0.881 (range: 1.00-5.00) in the healthy volunteers (p<0.001). We used receiver-operating characteristics (ROC) curve analysis to select two optimal plasma MYC/GAPDH cut-offs of 2.725 and 5.225. The sensitivity and specificity were 75.4% and 76.9% at 2.725, 38.6% and 100% at 5.225, respectively. The plasma MYC/GAPDH ratio from cancer patients was significantly correlated with the tissue MYC/GAPDH ratio (p=0.009), and tissue MYC status by FISH (p=0.024). Conclusions: These findings suggest that the plasma MYC/GAPDH ratio, as determined by real-time PCR, may be an alternative non-invasive approach for detecting gastric cancer. Clin Chem Lab Med 2009; 47:530-6.
ISSN
1434-6621
Language
English
URI
https://hdl.handle.net/10371/76706
DOI
https://doi.org/10.1515/CCLM.2009.126
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