Discovery and Validation of Salivary Extracellular RNA Biomarkers for Noninvasive Detection of Gastric Cancer

Author:

Li Feng12,Yoshizawa Janice M2,Kim Kyoung-Mee3,Kanjanapangka Julie2,Grogan Tristan R4,Wang Xiaoyan4,Elashoff David E4,Ishikawa Shigeo2,Chia David5,Liao Wei2,Akin David2,Yan Xinmin2,Lee Min-Sun6,Choi Rayun6,Kim Su-Mi6,Kang So-Young3,Bae Jae-Moon6,Sohn Tae-Sung6,Lee Jun-Ho6,Choi Min-Gew6,Min Byung-Hoon7,Lee Jun-Haeng7,Kim Jae J7,Kim Yong2,Kim Sung6,Wong David T W2

Affiliation:

1. Institute of Diagnostic in Chinese Medicine, Hunan University of Chinese Medicine, Changsha, Hunan, China

2. School of Dentistry, University of California, Los Angeles, CA

3. Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

4. Department of Medicine Statistics Core, David Geffen School of Medicine, University of California, Los Angeles, CA

5. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA

6. Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

7. Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

Abstract

Abstract 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.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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