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MicroRNAs in plasma of pancreatic ductal adenocarcinoma patients as novel blood-based biomarkers of disease

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TLDR
Observations show the feasibility of developing plasma miRNA profiling as a sensitive and specific blood-based biomarker assay for pancreatic cancer that has the potential of translation to the clinic with additional improvements in the future.
Abstract
Development of minimally invasive biomarker assays for early detection and effective clinical management of pancreatic cancer is urgently needed to reduce high morbidity and mortality associated with this malignancy We hypothesized that if aberrantly expressing microRNAs (miRNA) in pancreatic adenocarcinoma tissues are detected in blood plasma, then plasma profiling of these miRNAs might serve as a minimally invasive early detection biomarker assay for this malignancy By using a modified protocol to isolate and quantify plasma miRNAs from heparin-treated blood, we show that miRNA profiling in plasma can differentiate pancreatic adenocarcinoma patients from healthy controls We have profiled four miRNAs, miR-21, miR-210, miR-155, and miR-196a, all implicated in the development of pancreatic cancer with either proven or predicted target genes involved in critical cancer-associated cellular pathways Of these, miR-155 has recently been identified as a candidate biomarker of early pancreatic neoplasia, whereas elevated expression of miR196a has been shown to parallel progression of disease The results revealed a sensitivity of 64% and a specificity of 89% with the analyses of plasma levels for this panel of four miRNAs The area under the receiver operating characteristic curve were estimated at 082 and 078 without and with leave-one-out cross-validation scheme, respectively These observations, although a "proof of principle" finding at this time, show the feasibility of developing plasma miRNA profiling as a sensitive and specific blood-based biomarker assay for pancreatic cancer that has the potential of translation to the clinic with additional improvements in the future

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Citations
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Journal ArticleDOI

MicroRNAs: potential biomarkers for diagnosis and prognosis of different cancers

TL;DR: Seven miRNAs showing maximum dysregulation, either up- or down-regulation in the majority of cancers, were selected for a detailed presentation of their expression and evaluation of their potential as biomarkers in the diagnosis and prognosis of different cancers.
Journal ArticleDOI

MicroRNAs as tools and effectors for patient treatment in gastrointestinal carcinogenesis.

TL;DR: The role of miRNAs in gastrointestinal carcinogenesis and their potential use as novel biomarkers and therapeutics are summarized.
Journal ArticleDOI

Clinically relevant circulating microRNA profiling studies in pancreatic cancer using meta-analysis

TL;DR: It is demonstrated that multiple miRNAs were more accurate for diagnosing PaCa than a single miRNA, and future studies are still needed to confirm the diagnostic value of these pooled mi RNAs for PaCa.
Journal ArticleDOI

Suffocating cancer: hypoxia-associated epimutations as targets for cancer therapy

TL;DR: The therapeutic potential of epigenetic modifications occurring in hypoxia with particular reference to cancer and tumourigenesis is reviewed.
Journal ArticleDOI

Circulating peripheral blood mononuclear cells exhibit altered miRNA expression patterns in pancreatic cancer.

TL;DR: Evidence is examined for using circulating miRNAs to diagnose/prognose PDAC and the theory is that circulating blood cells monitor the patients’ physiological state and respond by altering their transcriptome and that this can be used to detect disease.
References
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Journal ArticleDOI

Analyzing real-time PCR data by the comparative C(T) method.

TL;DR: This protocol provides an overview of the comparative CT method for quantitative gene expression studies and various examples to present quantitative gene Expression data using this method.
Book

Pancreatic Cancer

Journal ArticleDOI

MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells.

TL;DR: It is shown that the highly malignant human brain tumor, glioblastoma, strongly over-expresses a specific miRNA, miR-21, which may contribute to the malignant phenotype by blocking expression of critical apoptosis-related genes.
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