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Open AccessJournal ArticleDOI

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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Emerging Roles of Non-Coding RNAs in the Hypoxic Response

TL;DR: All published studies agree that the induction of microRNA-210 (miR-210) is a consistent feature of the hypoxic response in both normal and transformed cells, and an increased knowledge about miR- 210’s actions may lead to novel diagnostic and therapeutic approaches in the cancer field.
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The effect and mechanism of miR196a in HepG2 cell.

TL;DR: It is demonstrated that miR-196a can effect the proliferation, the apoptosis and migration of HepG2 cell lines by gene HOXB8, caspase-3 regulation, however, there is no correlation between miRNA196a and P53 andHOXB9.
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Biofluids in hypobaric hypoxia: best possible use, investigative strategies and putative markers

TL;DR: This review concisely outlines the myriad results (particularly translational) in context of hypobaric hypoxia that have been observed in biological fluids, their collection strategies, storage strategies and ethical guidelines.
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Circulating Blood-Borne microRNAs as Biomarkers in Solid Tumors.

TL;DR: The tumor-specific profiles of blood-borne microRNAs are summarized and their potential utility for personalized medicine of solid tumors is discussed, suggesting that these molecules could be optimal noninvasive biomarkers in various diseases.
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Developing a nano-biosensor for early detection of pancreatic cancer

TL;DR: In this article, a simple electrochemical nanobiosensor for early detection of pancreatic cancer was developed using the newly emerged stable micro ribonucleic acid (miR-21) as a cancerassociated biomarker for diagnosis, prognosis or therapy response.
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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