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RNAscope compatibility with image analysis platforms for the quantification of tissue-based colorectal cancer biomarkers in archival formalin-fixed paraffin-embedded tissue.

Authors :
Morley-Bunker AE
Wiggins GAR
Currie MJ
Morrin HR
Whitehead MR
Eglinton T
Pearson J
Walker LC
Source :
Acta histochemica [Acta Histochem] 2021 Sep; Vol. 123 (6), pp. 151765. Date of Electronic Publication: 2021 Aug 05.
Publication Year :
2021

Abstract

RNAscope®, has emerged as an important in-situ hybridisation method to validate mRNA expression within single cells whilst preserving tissue morphology in histological samples. The aim of this research was to compare the utility of various open-source and commercial image analysis methods, to quantify mRNA transcripts identified by RNAscope within formalin fixed paraffin embedded (FFPE) histological samples and cell monolayer preparations. Examination of MLH1 expression from 10 histological FFPE colorectal cancer specimens using four image analysis tools (Colour Deconvolution, SpotStudio, WEKA and the LEICA RNA-ISH algorithm) showed the WEKA tool as having the greatest level of agreement with manual quantification. Comparing image analysis methods to qRT-PCR for quantifying MLH1, GFI1 and TNFRSF11A expression within two colorectal cell lines results suggest that these image analysis methods perform at a similar level to qRT-PCR. Furthermore, we describe the strengths and limitations for each image analysis method when used in combination with RNAscope assays. Our study concludes that there are several freely available and commercial image analysis tools that enable reliable RNA in situ expression analysis, however operators need to consider factors, such as expected expression levels of target genes, software usability and functionality.<br /> (Copyright © 2021 The Authors. Published by Elsevier GmbH.. All rights reserved.)

Details

Language :
English
ISSN :
1618-0372
Volume :
123
Issue :
6
Database :
MEDLINE
Journal :
Acta histochemica
Publication Type :
Academic Journal
Accession number :
34364165
Full Text :
https://doi.org/10.1016/j.acthis.2021.151765