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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

Circulating exosomal microRNAs as novel potential detection biomarkers in pancreatic cancer.

TL;DR: It is identified that serum ex-miRNAs, miRNA-21 and mi RNA-210 may be of value as potential biomarkers and therapeutic targets for the diagnosis and treatment of PC.
Journal ArticleDOI

Identification of circulating microRNAs as biomarkers in cancers: what have we got?

TL;DR: It is believed that great consideration should be taken in the development of circulating miRNAs as tumor biomarkers, due to poorly characterized preanalytical and analytical variables and the lack of a standardized measurement protocol.
Journal ArticleDOI

Primate-specific miRNA-637 inhibited tumorigenesis in human pancreatic ductal adenocarcinoma cells by suppressing Akt1 expression

TL;DR: In this paper, the authors found that miR-637 was significantly downregulated in pancreatic ductal adenocarcinoma (PDAC) cell lines and most of the PDAC specimens.
Journal ArticleDOI

Metabolomic profiling for biomarker discovery in pancreatic cancer

TL;DR: Mass spectrometry-based metabolomic profiling of human pancreas matched tumor and normal tissue shows significant alterations in the profiles of the tumor metabolome as compared to the normal tissue, offering an information-rich matrix for discovering novel candidate biomarkers with diagnostic or prognostic potential.
Journal ArticleDOI

Appraising MicroRNA-155 as a Noninvasive Diagnostic Biomarker for Cancer Detection: A Meta-Analysis.

TL;DR: Results from meta-analysis suggested that miR-155 had great potential as a novel noninvasive biomarker for human cancer detection, particularly when breast cancer or Caucasian is involved, however, well-designed cohort or case control studies with large sample size should be implemented to confirm the diagnostic value of mi R-155.
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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