Matches in SemOpenAlex for { <https://semopenalex.org/work/W2147173818> ?p ?o ?g. }
- W2147173818 endingPage "957.e7" @default.
- W2147173818 startingPage "949" @default.
- W2147173818 abstract "Background & AimsLack of detection technology for early pancreatic cancer invariably leads to a typical clinical presentation of incurable disease at initial diagnosis. New strategies and biomarkers for early detection are sorely needed. In this study, we have conducted a prospective sample collection and retrospective blinded validation to evaluate the performance and translational utilities of salivary transcriptomic biomarkers for the noninvasive detection of resectable pancreatic cancer.MethodsThe Affymetrix HG U133 Plus 2.0 Array (Affymetrix, Santa Clara, CA) was used to profile transcriptomes and discover altered gene expression in saliva supernatant. Biomarkers discovered from the microarray study were subjected to clinical validation using an independent sample set of 30 pancreatic cancer patients, 30 chronic pancreatitis patients, and 30 healthy controls.ResultsTwelve messenger RNA biomarkers were discovered and validated. The logistic regression model with the combination of 4 messenger RNA biomarkers (KRAS, MBD3L2, ACRV1, and DPM1) could differentiate pancreatic cancer patients from noncancer subjects (chronic pancreatitis and healthy control), yielding a receiver operating characteristic plot, area under the curve value of 0.971 with 90.0% sensitivity and 95.0% specificity.ConclusionsThe salivary biomarkers possess discriminatory power for the detection of resectable pancreatic cancer, with high specificity and sensitivity. This report provides the proof of concept of salivary biomarkers for the noninvasive detection of a systemic cancer and paves the way for prediction model validation study followed by pivotal clinical validation. Lack of detection technology for early pancreatic cancer invariably leads to a typical clinical presentation of incurable disease at initial diagnosis. New strategies and biomarkers for early detection are sorely needed. In this study, we have conducted a prospective sample collection and retrospective blinded validation to evaluate the performance and translational utilities of salivary transcriptomic biomarkers for the noninvasive detection of resectable pancreatic cancer. The Affymetrix HG U133 Plus 2.0 Array (Affymetrix, Santa Clara, CA) was used to profile transcriptomes and discover altered gene expression in saliva supernatant. Biomarkers discovered from the microarray study were subjected to clinical validation using an independent sample set of 30 pancreatic cancer patients, 30 chronic pancreatitis patients, and 30 healthy controls. Twelve messenger RNA biomarkers were discovered and validated. The logistic regression model with the combination of 4 messenger RNA biomarkers (KRAS, MBD3L2, ACRV1, and DPM1) could differentiate pancreatic cancer patients from noncancer subjects (chronic pancreatitis and healthy control), yielding a receiver operating characteristic plot, area under the curve value of 0.971 with 90.0% sensitivity and 95.0% specificity. The salivary biomarkers possess discriminatory power for the detection of resectable pancreatic cancer, with high specificity and sensitivity. This report provides the proof of concept of salivary biomarkers for the noninvasive detection of a systemic cancer and paves the way for prediction model validation study followed by pivotal clinical validation." @default.
- W2147173818 created "2016-06-24" @default.
- W2147173818 creator A5011480176 @default.
- W2147173818 creator A5029039848 @default.
- W2147173818 creator A5050051156 @default.
- W2147173818 creator A5070267955 @default.
- W2147173818 creator A5070990818 @default.
- W2147173818 creator A5071798264 @default.
- W2147173818 creator A5086335637 @default.
- W2147173818 creator A5087543035 @default.
- W2147173818 date "2010-03-01" @default.
- W2147173818 modified "2023-10-18" @default.
- W2147173818 title "Salivary Transcriptomic Biomarkers for Detection of Resectable Pancreatic Cancer" @default.
- W2147173818 cites W1611896441 @default.
- W2147173818 cites W1965090530 @default.
- W2147173818 cites W1965967919 @default.
- W2147173818 cites W1967196349 @default.
- W2147173818 cites W1972026849 @default.
- W2147173818 cites W1977352336 @default.
- W2147173818 cites W1982821807 @default.
- W2147173818 cites W1988675408 @default.
- W2147173818 cites W1994015078 @default.
- W2147173818 cites W2011437253 @default.
- W2147173818 cites W2012579372 @default.
- W2147173818 cites W2019223199 @default.
- W2147173818 cites W2026105846 @default.
- W2147173818 cites W2027872382 @default.
- W2147173818 cites W2030955639 @default.
- W2147173818 cites W2032579588 @default.
- W2147173818 cites W2034223072 @default.
- W2147173818 cites W2036448141 @default.
- W2147173818 cites W2100185080 @default.
- W2147173818 cites W2104960492 @default.
- W2147173818 cites W2106489008 @default.
- W2147173818 cites W2108338691 @default.
- W2147173818 cites W2108408152 @default.
- W2147173818 cites W2113272687 @default.
- W2147173818 cites W2115757940 @default.
- W2147173818 cites W2116152377 @default.
- W2147173818 cites W2120489590 @default.
- W2147173818 cites W2121032725 @default.
- W2147173818 cites W2121185785 @default.
- W2147173818 cites W2123607020 @default.
- W2147173818 cites W2123768348 @default.
- W2147173818 cites W2124262378 @default.
- W2147173818 cites W2127839469 @default.
- W2147173818 cites W2146066097 @default.
- W2147173818 cites W2156536854 @default.
- W2147173818 cites W2157088766 @default.
- W2147173818 cites W2157142504 @default.
- W2147173818 cites W2157825442 @default.
- W2147173818 cites W2159435688 @default.
- W2147173818 cites W2166648052 @default.
- W2147173818 cites W2167244585 @default.
- W2147173818 cites W2168897896 @default.
- W2147173818 doi "https://doi.org/10.1053/j.gastro.2009.11.010" @default.
- W2147173818 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2831159" @default.
- W2147173818 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19931263" @default.
- W2147173818 hasPublicationYear "2010" @default.
- W2147173818 type Work @default.
- W2147173818 sameAs 2147173818 @default.
- W2147173818 citedByCount "269" @default.
- W2147173818 countsByYear W21471738182012 @default.
- W2147173818 countsByYear W21471738182013 @default.
- W2147173818 countsByYear W21471738182014 @default.
- W2147173818 countsByYear W21471738182015 @default.
- W2147173818 countsByYear W21471738182016 @default.
- W2147173818 countsByYear W21471738182017 @default.
- W2147173818 countsByYear W21471738182018 @default.
- W2147173818 countsByYear W21471738182019 @default.
- W2147173818 countsByYear W21471738182020 @default.
- W2147173818 countsByYear W21471738182021 @default.
- W2147173818 countsByYear W21471738182022 @default.
- W2147173818 countsByYear W21471738182023 @default.
- W2147173818 crossrefType "journal-article" @default.
- W2147173818 hasAuthorship W2147173818A5011480176 @default.
- W2147173818 hasAuthorship W2147173818A5029039848 @default.
- W2147173818 hasAuthorship W2147173818A5050051156 @default.
- W2147173818 hasAuthorship W2147173818A5070267955 @default.
- W2147173818 hasAuthorship W2147173818A5070990818 @default.
- W2147173818 hasAuthorship W2147173818A5071798264 @default.
- W2147173818 hasAuthorship W2147173818A5086335637 @default.
- W2147173818 hasAuthorship W2147173818A5087543035 @default.
- W2147173818 hasBestOaLocation W21471738181 @default.
- W2147173818 hasConcept C104317684 @default.
- W2147173818 hasConcept C121608353 @default.
- W2147173818 hasConcept C126322002 @default.
- W2147173818 hasConcept C143998085 @default.
- W2147173818 hasConcept C150194340 @default.
- W2147173818 hasConcept C186836561 @default.
- W2147173818 hasConcept C2775967933 @default.
- W2147173818 hasConcept C2780210213 @default.
- W2147173818 hasConcept C2781187634 @default.
- W2147173818 hasConcept C2781197716 @default.
- W2147173818 hasConcept C526805850 @default.
- W2147173818 hasConcept C55493867 @default.
- W2147173818 hasConcept C58471807 @default.
- W2147173818 hasConcept C71924100 @default.