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Open AccessJournal ArticleDOI

Distribution of microRNA biomarker candidates in solid tissues and body fluids

TLDR
The Human miRNA Tissue Atlas is reported, and the web-based repository now hosting 982 full miRNomes all of which are measured by the same microarray technology, identified miRNAs that are rather specific for tissues.
Abstract
Small non-coding RNAs, especially microRNAs, are discussed as promising biomarkers for a substantial number of human pathologies. A broad understanding in which solid tissues, cell types or body fluids a microRNA is expressed helps also to understand and to improve the suitability of miRNAs as non- or minimally-invasive disease markers. We recently reported the Human miRNA Tissue Atlas ( http://www.ccb.uni-saarland.de/tissueatlas ) containing 105 miRNA profiles of 31 organs from 2 corpses. We subsequently added miRNA profiles measured by others and us using the same array technology as for the first version of the Human miRNA Tissue Atlas. The latter profiles stem from 163 solid organs including lung, prostate and gastric tissue, from 253 whole blood samples and 66 fractioned blood cell isolates, from body fluids including 72 serum samples, 278 plasma samples, 29 urine samples, and 16 saliva samples and from different collection and storage conditions. While most miRNAs are ubiquitous abundant in solid tissues and whole blood, we also identified miRNAs that are rather specific for tissues. Our web-based repository now hosting 982 full miRNomes all of which are measured by the same microarray technology. The knowledge of these variant abundances of miRNAs in solid tissues, in whole blood and in other body fluids is essential to judge the value of miRNAs as biomarker.

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Citations
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Journal ArticleDOI

Trends in the development of miRNA bioinformatics tools.

TL;DR: Five key trends were observed: miRNA identification and target prediction have been hot spots in the past decade; manual curation and TM are the main methods for collecting miRNA knowledge from literature; most early tools are well maintained and widely used; however, novel ones have begun to emerge and disease-associated miRNA tools are emerging.
Journal ArticleDOI

Total Extracellular Small RNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects.

TL;DR: A systematic analysis of small exRNAs present in each biofluid, as well as an analysis of exogenous RNAs are provided, finding that a large number of RNA fragments in plasma and urine have sequences that are assigned to YRNA and tRNA fragments respectively.
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MicroRNA in diagnosis and therapy monitoring of early-stage triple-negative breast cancer

TL;DR: It is reported that miRNA expression measured from blood facilitates early and minimally-invasive diagnosis of basal-like TNBC and that blood-borne miRNA profiles monitored over time have potential to predict pathological complete response (pCR).
Journal ArticleDOI

Circulating miRNA analysis for cancer diagnostics and therapy.

TL;DR: This review provides a comprehensive overview of circulating miRNA analysis and highlights the importance of sampling and quality control, the technical aspects of miRNA extraction and quantification, recommendations for downstream analysis and conclude with future perspectives.
References
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Journal ArticleDOI

A mammalian microRNA expression atlas based on small RNA library sequencing.

TL;DR: A relatively small set of miRNAs, many of which are ubiquitously expressed, account for most of the differences in miRNA profiles between cell lineages and tissues.
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Distribution of miRNA expression across human tissues

TL;DR: A human miRNA tissue atlas is presented by determining the abundance of 1997 miRNAs in 61 tissue biopsies of different organs from two individuals collected post-mortem, revealing that tissues like several areas of the brain clustered together andMiRNAs that were highly abundant in certain human tissues were likewise abundant in according rat tissues.
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Cardiac-specific miRNA in cardiogenesis, heart function, and cardiac pathology (with focus on myocardial infarction).

TL;DR: Great cardiospecific capacity of these miRNAs is very helpful for enhancing regenerative properties and survival of stem cell and cardiac progenitor transplants and for reprogramming of mature non-cardiac cells to cardiomyocytes.
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Targeting oncomiRNAs and mimicking tumor suppressor miRNAs: Νew trends in the development of miRNA therapeutic strategies in oncology (Review).

TL;DR: This review focuses on the most promising examples potentially leading to the development of anticancer, miRNA-based therapeutic protocols and concludes that the combination of anti-miRNA and miRNA replacement strategies may lead to excellent results, in terms of antitumor effects.
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The transcardiac gradient of cardio‐microRNAs in the failing heart

TL;DR: The transcardiac gradient of 84 cardio‐microRNAs in healthy and failing hearts is evaluated to determine which microRNAs are released or absorbed by the myocardium in heart failure.
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