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SAL_23183 details
Primary information
SALIDSAL_23183
Biomarker namemiR-486-5p
Biomarker TypeDiagnostic
Sampling Method39 patients with EC from age, gende-, and ethnically matched with 19 healthy individuals, were collected as controls
Collection MethodSubjects were asked to refrain from eating, drinking, smoking, and oral hygiene procedures for at least 2 hours before the collection.
Analysis MethodqRT-PCR
Collection SiteWhole Saliva
Disease CategoryCancer
Disease/ConditionEsophageal Cancer
Disease SubtypeEsophageal Squamous Cell Carcinoma
Fold Change/ ConcentrationNA
Up/DownregulatedNA
ExosomalNA
OrganismHomo sapiens
PMID23560033
Year of Publication2013
Biomarker IDhsa-miR-486-5p
Biomarker CategorymiRNA
SequenceUCCUGUACUGAGCUGCCCCGAG
Title of studySalivary microRNAs as promising biomarkers for detection of esophageal cancer
Abstract of studyBACKGROUND AND PURPOSE: Tissue microRNAs (miRNAs) can detect cancers and predict prognosis. Several recent studies reported that tissue, plasma, and saliva miRNAs share similar expression profiles. In this study, we investigated the discriminatory power of salivary miRNAs (including whole saliva and saliva supernatant) for detection of esophageal cancer.MATERIALS AND METHODS: By Agilent microarray, six deregulated miRNAs from whole saliva samples from seven patients with esophageal cancer and three healthy controls were selected. The six selected miRNAs were subjected to validation of their expression levels by RT-qPCR using both whole saliva and saliva supernatant samples from an independent set of 39 patients with esophageal cancer and 19 healthy controls.RESULTS: Six miRNAs (miR-10b*, miR-144, miR-21, miR-451, miR-486-5p, and miR-634) were identified as targets by Agilent microarray. After validation by RT-qPCR, miR-10b*, miR-144, and miR-451 in whole saliva and miR-10b*, miR-144, miR-21, and miR-451 in saliva supernatant were significantly upregulated in patients, with sensitivities of 89.7, 92.3, 84.6, 79.5, 43.6, 89.7, and 51.3% and specificities of 57.9, 47.4, 57.9%, 57.9, 89.5, 47.4, and 84.2%, respectively.CONCLUSIONS: We found distinctive miRNAs for esophageal cancer in both whole saliva and saliva supernatant. These miRNAs possess discriminatory power for detection of esophageal cancer. Because saliva collection is noninvasive and convenient, salivary miRNAs show great promise as biomarkers for detection of esophageal cancer in areas at high risk.