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DETECTing Merkel Cell Polyomavirus in Merkel Tumors

Merkel cell carcinoma (MCC) is a rare, aggressive skin cancer caused either by Merkel cell polyomavirus (MCV) T antigen expression, post-integration (~80% cases), or by UV-mediated DNA damage. Interestingly, overall survival of MCV-positive Merkel cell carcinoma patients is better, making this diffe...

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Autores principales: Arora, Reety, Gupta, Komal, Vijaykumar, Anjali, Krishna, Sudhir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011098/
https://www.ncbi.nlm.nih.gov/pubmed/32118036
http://dx.doi.org/10.3389/fmolb.2020.00010
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author Arora, Reety
Gupta, Komal
Vijaykumar, Anjali
Krishna, Sudhir
author_facet Arora, Reety
Gupta, Komal
Vijaykumar, Anjali
Krishna, Sudhir
author_sort Arora, Reety
collection PubMed
description Merkel cell carcinoma (MCC) is a rare, aggressive skin cancer caused either by Merkel cell polyomavirus (MCV) T antigen expression, post-integration (~80% cases), or by UV-mediated DNA damage. Interestingly, overall survival of MCV-positive Merkel cell carcinoma patients is better, making this differential information of significant diagnostic and prognostic value. Also, MCV provides a direct target for therapy in MCC patients. Currently, the methods used for diagnosis of MCV in tumors are often discordant and unreliable. Here we used a guided molecular scissors based–DNA Endonuclease Targeted CRISPR Trans Reporter (DETECTR) technique to develop an in vitro molecular diagnostic tool for MCV-positive MCC. DETECTR couples recombinase polymerase based amplification of target MCV DNA with Cas12a mediated detection. CRISPR diagnostics couple specific detection followed by cutting of the pathogenic DNA by the Cas enzyme–gRNA complex, with non-specific cutting of ssDNA that provides a measurable visual cue. To detect MCV DNA in MCC, we designed Cas12a gRNAs targeting the MCV DNA and tested their targeting efficiency, and sensitivity using a fluorophore quencher labeled reporter assay. We show that MCV DETECTR system can detect MCV integrated in Merkel tumor rapidly, specifically and with femto-molar sensitivity. Our study is a preliminary, proof-of-principle analysis showing the use of CRISPR for MCV diagnosis. Further validation in human tumor samples is needed for its clinical use in the near future. This new system is promising and we hope it can be coupled with immunohistochemical studies to diagnose the viral status of MCC in clinics soon.
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spelling pubmed-70110982020-02-28 DETECTing Merkel Cell Polyomavirus in Merkel Tumors Arora, Reety Gupta, Komal Vijaykumar, Anjali Krishna, Sudhir Front Mol Biosci Molecular Biosciences Merkel cell carcinoma (MCC) is a rare, aggressive skin cancer caused either by Merkel cell polyomavirus (MCV) T antigen expression, post-integration (~80% cases), or by UV-mediated DNA damage. Interestingly, overall survival of MCV-positive Merkel cell carcinoma patients is better, making this differential information of significant diagnostic and prognostic value. Also, MCV provides a direct target for therapy in MCC patients. Currently, the methods used for diagnosis of MCV in tumors are often discordant and unreliable. Here we used a guided molecular scissors based–DNA Endonuclease Targeted CRISPR Trans Reporter (DETECTR) technique to develop an in vitro molecular diagnostic tool for MCV-positive MCC. DETECTR couples recombinase polymerase based amplification of target MCV DNA with Cas12a mediated detection. CRISPR diagnostics couple specific detection followed by cutting of the pathogenic DNA by the Cas enzyme–gRNA complex, with non-specific cutting of ssDNA that provides a measurable visual cue. To detect MCV DNA in MCC, we designed Cas12a gRNAs targeting the MCV DNA and tested their targeting efficiency, and sensitivity using a fluorophore quencher labeled reporter assay. We show that MCV DETECTR system can detect MCV integrated in Merkel tumor rapidly, specifically and with femto-molar sensitivity. Our study is a preliminary, proof-of-principle analysis showing the use of CRISPR for MCV diagnosis. Further validation in human tumor samples is needed for its clinical use in the near future. This new system is promising and we hope it can be coupled with immunohistochemical studies to diagnose the viral status of MCC in clinics soon. Frontiers Media S.A. 2020-02-04 /pmc/articles/PMC7011098/ /pubmed/32118036 http://dx.doi.org/10.3389/fmolb.2020.00010 Text en Copyright © 2020 Arora, Gupta, Vijaykumar and Krishna. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Arora, Reety
Gupta, Komal
Vijaykumar, Anjali
Krishna, Sudhir
DETECTing Merkel Cell Polyomavirus in Merkel Tumors
title DETECTing Merkel Cell Polyomavirus in Merkel Tumors
title_full DETECTing Merkel Cell Polyomavirus in Merkel Tumors
title_fullStr DETECTing Merkel Cell Polyomavirus in Merkel Tumors
title_full_unstemmed DETECTing Merkel Cell Polyomavirus in Merkel Tumors
title_short DETECTing Merkel Cell Polyomavirus in Merkel Tumors
title_sort detecting merkel cell polyomavirus in merkel tumors
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011098/
https://www.ncbi.nlm.nih.gov/pubmed/32118036
http://dx.doi.org/10.3389/fmolb.2020.00010
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