A novel approach for microRNA in situ hybridization using locked nucleic acid probes

Research output: Contribution to journalJournal articleResearchpeer-review

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A novel approach for microRNA in situ hybridization using locked nucleic acid probes. / Paulsen, Isabella W.; Bzorek, Michael; Olsen, Jesper; Grum-Schwensen, Birgitte; Troelsen, Jesper T.; Pedersen, Ole B.

In: Scientific Reports, Vol. 11, No. 1, 4504, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Paulsen, IW, Bzorek, M, Olsen, J, Grum-Schwensen, B, Troelsen, JT & Pedersen, OB 2021, 'A novel approach for microRNA in situ hybridization using locked nucleic acid probes', Scientific Reports, vol. 11, no. 1, 4504. https://doi.org/10.1038/s41598-021-83888-5

APA

Paulsen, I. W., Bzorek, M., Olsen, J., Grum-Schwensen, B., Troelsen, J. T., & Pedersen, O. B. (2021). A novel approach for microRNA in situ hybridization using locked nucleic acid probes. Scientific Reports, 11(1), [4504]. https://doi.org/10.1038/s41598-021-83888-5

Vancouver

Paulsen IW, Bzorek M, Olsen J, Grum-Schwensen B, Troelsen JT, Pedersen OB. A novel approach for microRNA in situ hybridization using locked nucleic acid probes. Scientific Reports. 2021;11(1). 4504. https://doi.org/10.1038/s41598-021-83888-5

Author

Paulsen, Isabella W. ; Bzorek, Michael ; Olsen, Jesper ; Grum-Schwensen, Birgitte ; Troelsen, Jesper T. ; Pedersen, Ole B. / A novel approach for microRNA in situ hybridization using locked nucleic acid probes. In: Scientific Reports. 2021 ; Vol. 11, No. 1.

Bibtex

@article{c5b2a2edd3e64698b2f207caef3c6da8,
title = "A novel approach for microRNA in situ hybridization using locked nucleic acid probes",
abstract = "Identification of target tissue microRNAs (miR) using in situ hybridization (ISH), with digoxigenin-labeled locked nucleic acid (LNA) probes, is influenced by preanalytic parameters. To determine the best retrieval method for common microRNAs, a multiblock composed of paraffin-embedded tonsil, cervix, placenta, and hyperplastic prostate tissue were included. Tissue were fixed in 10% formalin in a range of 5–144 hours (h). Cut sections (5 μm) from the multiblock were subjected to combinations of pretreatment procedures: variable periods of proteinase K (PK) digestion or Heat-induced microRNA Retrieval (HmiRR) using target retrieval solution (TRS) pH 6.1 or 9, with or without enzymatic treatment (pepsin). Results for the overall categories: TRS pH 9 versus PK; p = 2.9e−23, TRS pH 9 versus TRS pH 6.1; p = 1.1e−14, TRS pH 6.1 versus PK; p = 2.9e−03. A long fixation time, resulted in the best microRNA preservation and staining intensity (long vs. short: p = 3.5e−47, long vs. moderate: p = 1.6e−44, moderate vs. short: p = 4.3e−16), was enhanced using HmiRR TRS pH 9 with or without pepsin providing high sensitivity and specificity. These observations conflict with other ISH techniques (e.g., messenger ribonucleic acid), which typically require shorter fixation periods, and therefore, further studies are warranted.",
author = "Paulsen, {Isabella W.} and Michael Bzorek and Jesper Olsen and Birgitte Grum-Schwensen and Troelsen, {Jesper T.} and Pedersen, {Ole B.}",
year = "2021",
doi = "10.1038/s41598-021-83888-5",
language = "English",
volume = "11",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "nature publishing group",
number = "1",

}

RIS

TY - JOUR

T1 - A novel approach for microRNA in situ hybridization using locked nucleic acid probes

AU - Paulsen, Isabella W.

AU - Bzorek, Michael

AU - Olsen, Jesper

AU - Grum-Schwensen, Birgitte

AU - Troelsen, Jesper T.

AU - Pedersen, Ole B.

PY - 2021

Y1 - 2021

N2 - Identification of target tissue microRNAs (miR) using in situ hybridization (ISH), with digoxigenin-labeled locked nucleic acid (LNA) probes, is influenced by preanalytic parameters. To determine the best retrieval method for common microRNAs, a multiblock composed of paraffin-embedded tonsil, cervix, placenta, and hyperplastic prostate tissue were included. Tissue were fixed in 10% formalin in a range of 5–144 hours (h). Cut sections (5 μm) from the multiblock were subjected to combinations of pretreatment procedures: variable periods of proteinase K (PK) digestion or Heat-induced microRNA Retrieval (HmiRR) using target retrieval solution (TRS) pH 6.1 or 9, with or without enzymatic treatment (pepsin). Results for the overall categories: TRS pH 9 versus PK; p = 2.9e−23, TRS pH 9 versus TRS pH 6.1; p = 1.1e−14, TRS pH 6.1 versus PK; p = 2.9e−03. A long fixation time, resulted in the best microRNA preservation and staining intensity (long vs. short: p = 3.5e−47, long vs. moderate: p = 1.6e−44, moderate vs. short: p = 4.3e−16), was enhanced using HmiRR TRS pH 9 with or without pepsin providing high sensitivity and specificity. These observations conflict with other ISH techniques (e.g., messenger ribonucleic acid), which typically require shorter fixation periods, and therefore, further studies are warranted.

AB - Identification of target tissue microRNAs (miR) using in situ hybridization (ISH), with digoxigenin-labeled locked nucleic acid (LNA) probes, is influenced by preanalytic parameters. To determine the best retrieval method for common microRNAs, a multiblock composed of paraffin-embedded tonsil, cervix, placenta, and hyperplastic prostate tissue were included. Tissue were fixed in 10% formalin in a range of 5–144 hours (h). Cut sections (5 μm) from the multiblock were subjected to combinations of pretreatment procedures: variable periods of proteinase K (PK) digestion or Heat-induced microRNA Retrieval (HmiRR) using target retrieval solution (TRS) pH 6.1 or 9, with or without enzymatic treatment (pepsin). Results for the overall categories: TRS pH 9 versus PK; p = 2.9e−23, TRS pH 9 versus TRS pH 6.1; p = 1.1e−14, TRS pH 6.1 versus PK; p = 2.9e−03. A long fixation time, resulted in the best microRNA preservation and staining intensity (long vs. short: p = 3.5e−47, long vs. moderate: p = 1.6e−44, moderate vs. short: p = 4.3e−16), was enhanced using HmiRR TRS pH 9 with or without pepsin providing high sensitivity and specificity. These observations conflict with other ISH techniques (e.g., messenger ribonucleic acid), which typically require shorter fixation periods, and therefore, further studies are warranted.

U2 - 10.1038/s41598-021-83888-5

DO - 10.1038/s41598-021-83888-5

M3 - Journal article

C2 - 33627751

AN - SCOPUS:85101751941

VL - 11

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

IS - 1

M1 - 4504

ER -

ID: 258902454