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Discovery and Validation of Salivary Extracellular RNA Biomarkers for Noninvasive Detection of Gastric Cancer
Author(s) -
Feng Li,
Janice Yoshizawa,
KyoungMee Kim,
Julie Kanjanapangka,
Tristan Grogan,
Xiaoyan Wang,
David Elashoff,
Shigeo Ishikawa,
David Chia,
Wei Liao,
David Akin,
Xinmin Yan,
Min-Sun Lee,
Rayun Choi,
Sumi Kim,
Soyoung Kang,
Jae-Moon Bae,
Tae-Sung Sohn,
Jun Ho Lee,
Min-Gew Choi,
ByungHoon Min,
Jun-Haeng Lee,
JaeHan Kim,
Yong Kim,
Sung Kim,
David T. Wong
Publication year - 2018
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/clinchem.2018.290569
Subject(s) - saliva , biomarker , medicine , cohort , cancer , microrna , biomarker discovery , area under the curve , oncology , real time polymerase chain reaction , gastroenterology , biology , gene , proteomics , biochemistry
BACKGROUND Biomarkers are needed for noninvasive early detection of gastric cancer (GC). We investigated salivary extracellular RNA (exRNA) biomarkers as potential clinical evaluation tools for GC. METHODS Unstimulated whole saliva samples were prospectively collected from 294 individuals (163 GC and 131 non-GC patients) who underwent endoscopic evaluation at the Samsung Medical Center in Korea. Salivary transcriptomes of 63 GC and 31 non-GC patients were profiled, and mRNA biomarker candidates were verified with reverse transcription quantitative real-time PCR (RT-qPCR). In parallel, microRNA (miRNA) biomarkers were profiled and verified with saliva samples from 10 GC and 10 non-GC patients. Candidate biomarkers were validated with RT-qPCR in an independent cohort of 100/100 saliva samples from GC and non-GC patients. Validated individual markers were configured into a best performance panel. RESULTS We identified 30 mRNA and 15 miRNA candidates whose expression pattern associated with the presence of GC. Among them, 12 mRNA and 6 miRNA candidates were verified with the discovery cohort by RT-qPCR and further validated with the independent cohort (n = 200). The configured biomarker panel consisted of 3 mRNAs (SPINK7, PPL, and SEMA4B) and 2 miRNAs (MIR140-5p and MIR301a), which were all significantly down-regulated in the GC group, and yielded an area under the ROC curve (AUC) of 0.81 (95% CI, 0.72–0.89). When combined with demographic factors, the AUC of the biomarker panel reached 0.87 (95% CI, 0.80–0.93). CONCLUSIONS We have discovered and validated a panel of salivary exRNA biomarkers with credible clinical performance for the detection of GC. Our study demonstrates the potential utility of salivary exRNA biomarkers in screening and risk assessment for GC.

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