Evaluation of microRNA stability in feces from healthy dogs

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Evaluation of microRNA stability in feces from healthy dogs. / Cirera, Susanna; Willumsen, Line M.; Johansen, Thea T.; Nielsen, Lise N.

In: Veterinary Clinical Pathology, Vol. 47, No. 1, 03.2018, p. 115-121.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Cirera, S, Willumsen, LM, Johansen, TT & Nielsen, LN 2018, 'Evaluation of microRNA stability in feces from healthy dogs', Veterinary Clinical Pathology, vol. 47, no. 1, pp. 115-121. https://doi.org/10.1111/vcp.12566

APA

Cirera, S., Willumsen, L. M., Johansen, T. T., & Nielsen, L. N. (2018). Evaluation of microRNA stability in feces from healthy dogs. Veterinary Clinical Pathology, 47(1), 115-121. https://doi.org/10.1111/vcp.12566

Vancouver

Cirera S, Willumsen LM, Johansen TT, Nielsen LN. Evaluation of microRNA stability in feces from healthy dogs. Veterinary Clinical Pathology. 2018 Mar;47(1):115-121. https://doi.org/10.1111/vcp.12566

Author

Cirera, Susanna ; Willumsen, Line M. ; Johansen, Thea T. ; Nielsen, Lise N. / Evaluation of microRNA stability in feces from healthy dogs. In: Veterinary Clinical Pathology. 2018 ; Vol. 47, No. 1. pp. 115-121.

Bibtex

@article{108d897d50204e2386165ed769c19c88,
title = "Evaluation of microRNA stability in feces from healthy dogs",
abstract = "Background: Gastrointestinal cancer accounts for approximately 8% of all canine malignancies. Early detection of cancer may have a tremendous impact on both treatment options and prognosis. MicroRNAs (miRNAs), a class of noncoding RNAs that can be found stably expressed in body fluids and feces, have been suggested as valuable human cancer biomarkers. Objectives: The purpose of the study was to investigate the feasibility of detecting miRNAs in canine feces and to determine the miRNA stability in fecal samples stored at different temperatures for different duration. Methods: The levels of 4 Canine familiaris (cfa) miRNAs (cfa-miR-16, cfa-miR-20a, cfa-miR-21, and cfa-miR-92a) were investigated by quantitative real-time PCR(qPCR) in fecal samples from 10 healthy dogs. Fecal samples were collected at 3 different time points and samples from the first time point were stored at different temperatures and for a different duration. Results: A statistically significant difference was found in miRNA levels from samples stored at room temperature compared with samples stored at −20°C for cfa-miR-16 and cfa-miR-21. No significant difference was found in the level of the investigated miRNAs over time. Conclusions: Overall, miRNAs are present in dog feces at measurable levels. Some miRNAs seem to be subject to a higher degree of degradation in samples stored at room temperature for 24 hours compared with samples frozen after collection at −20°C. The investigated miRNAs were stably expressed over time. This study provides the basis for further research on miRNA expression profiles as biomarkers for gastrointestinal cancer in dogs.",
keywords = "Biomarker, canine, diagnostics, feces, microRNA profiling, qPCR, Male, Reference Values, MicroRNAs/chemistry, RNA Stability, Feasibility Studies, Animals, Dogs, Female, Feces/chemistry",
author = "Susanna Cirera and Willumsen, {Line M.} and Johansen, {Thea T.} and Nielsen, {Lise N.}",
year = "2018",
month = mar,
doi = "10.1111/vcp.12566",
language = "English",
volume = "47",
pages = "115--121",
journal = "Veterinary Clinical Pathology",
issn = "0275-6382",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Evaluation of microRNA stability in feces from healthy dogs

AU - Cirera, Susanna

AU - Willumsen, Line M.

AU - Johansen, Thea T.

AU - Nielsen, Lise N.

PY - 2018/3

Y1 - 2018/3

N2 - Background: Gastrointestinal cancer accounts for approximately 8% of all canine malignancies. Early detection of cancer may have a tremendous impact on both treatment options and prognosis. MicroRNAs (miRNAs), a class of noncoding RNAs that can be found stably expressed in body fluids and feces, have been suggested as valuable human cancer biomarkers. Objectives: The purpose of the study was to investigate the feasibility of detecting miRNAs in canine feces and to determine the miRNA stability in fecal samples stored at different temperatures for different duration. Methods: The levels of 4 Canine familiaris (cfa) miRNAs (cfa-miR-16, cfa-miR-20a, cfa-miR-21, and cfa-miR-92a) were investigated by quantitative real-time PCR(qPCR) in fecal samples from 10 healthy dogs. Fecal samples were collected at 3 different time points and samples from the first time point were stored at different temperatures and for a different duration. Results: A statistically significant difference was found in miRNA levels from samples stored at room temperature compared with samples stored at −20°C for cfa-miR-16 and cfa-miR-21. No significant difference was found in the level of the investigated miRNAs over time. Conclusions: Overall, miRNAs are present in dog feces at measurable levels. Some miRNAs seem to be subject to a higher degree of degradation in samples stored at room temperature for 24 hours compared with samples frozen after collection at −20°C. The investigated miRNAs were stably expressed over time. This study provides the basis for further research on miRNA expression profiles as biomarkers for gastrointestinal cancer in dogs.

AB - Background: Gastrointestinal cancer accounts for approximately 8% of all canine malignancies. Early detection of cancer may have a tremendous impact on both treatment options and prognosis. MicroRNAs (miRNAs), a class of noncoding RNAs that can be found stably expressed in body fluids and feces, have been suggested as valuable human cancer biomarkers. Objectives: The purpose of the study was to investigate the feasibility of detecting miRNAs in canine feces and to determine the miRNA stability in fecal samples stored at different temperatures for different duration. Methods: The levels of 4 Canine familiaris (cfa) miRNAs (cfa-miR-16, cfa-miR-20a, cfa-miR-21, and cfa-miR-92a) were investigated by quantitative real-time PCR(qPCR) in fecal samples from 10 healthy dogs. Fecal samples were collected at 3 different time points and samples from the first time point were stored at different temperatures and for a different duration. Results: A statistically significant difference was found in miRNA levels from samples stored at room temperature compared with samples stored at −20°C for cfa-miR-16 and cfa-miR-21. No significant difference was found in the level of the investigated miRNAs over time. Conclusions: Overall, miRNAs are present in dog feces at measurable levels. Some miRNAs seem to be subject to a higher degree of degradation in samples stored at room temperature for 24 hours compared with samples frozen after collection at −20°C. The investigated miRNAs were stably expressed over time. This study provides the basis for further research on miRNA expression profiles as biomarkers for gastrointestinal cancer in dogs.

KW - Biomarker

KW - canine

KW - diagnostics

KW - feces

KW - microRNA profiling

KW - qPCR

KW - Male

KW - Reference Values

KW - MicroRNAs/chemistry

KW - RNA Stability

KW - Feasibility Studies

KW - Animals

KW - Dogs

KW - Female

KW - Feces/chemistry

U2 - 10.1111/vcp.12566

DO - 10.1111/vcp.12566

M3 - Journal article

C2 - 29393972

AN - SCOPUS:85041313275

VL - 47

SP - 115

EP - 121

JO - Veterinary Clinical Pathology

JF - Veterinary Clinical Pathology

SN - 0275-6382

IS - 1

ER -

ID: 194910585