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Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer

We compared the performance of the 3D-Gene® mutation assay (3D-Gene® KRAS mutation assay kit) with the Scorpion-ARMS (therascreen® KRAS RGQ PCR Kit) and Luminex (MEBGEN™ KRAS kit) assays for the detection of KRAS mutations in formalin-fixed, paraffin-embedded tissue samples from 150 patients diagnos...

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Autores principales: Sakai, Kazuko, Yoneshige, Azusa, Ito, Akihiko, Ueda, Yoji, Kondo, Satoshi, Nobumasa, Hitoshi, Fujita, Yoshihiko, Togashi, Yosuke, Terashima, Masato, De Velasco, Marco A, Tomida, Shuta, Nishio, Kazuto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320212/
https://www.ncbi.nlm.nih.gov/pubmed/25674493
http://dx.doi.org/10.1186/2193-1801-4-7
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author Sakai, Kazuko
Yoneshige, Azusa
Ito, Akihiko
Ueda, Yoji
Kondo, Satoshi
Nobumasa, Hitoshi
Fujita, Yoshihiko
Togashi, Yosuke
Terashima, Masato
De Velasco, Marco A
Tomida, Shuta
Nishio, Kazuto
author_facet Sakai, Kazuko
Yoneshige, Azusa
Ito, Akihiko
Ueda, Yoji
Kondo, Satoshi
Nobumasa, Hitoshi
Fujita, Yoshihiko
Togashi, Yosuke
Terashima, Masato
De Velasco, Marco A
Tomida, Shuta
Nishio, Kazuto
author_sort Sakai, Kazuko
collection PubMed
description We compared the performance of the 3D-Gene® mutation assay (3D-Gene® KRAS mutation assay kit) with the Scorpion-ARMS (therascreen® KRAS RGQ PCR Kit) and Luminex (MEBGEN™ KRAS kit) assays for the detection of KRAS mutations in formalin-fixed, paraffin-embedded tissue samples from 150 patients diagnosed with colorectal cancer. DNA was extracted from the paraffin-embedded tissue samples with or without macrodissection under hematoxylin and eosin staining and the KRAS mutation status was independently determined using these assays. Discordant results were re-analyzed by Sanger sequencing. Mutation detection analysis was successfully performed in all 150 specimens using the 3D-Gene® mutation assay without an invalid case. The concordance rate between the 3D-Gene® mutation assay and Scorpion-ARMS or Luminex was 98.7% (148/150). KRAS mutations were detected at a frequency of 35.3% (53/150) in colorectal cancer specimens. Three discrepant cases were found between the three assays. Overall, our results demonstrate a high concordance rate of between the 3D-Gene® mutation assay and the two existing in-vitro diagnostics kits. All three assays proved to be validated methods for detecting clinically significant KRAS mutations in paraffin-embedded tissue samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-4-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-43202122015-02-11 Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer Sakai, Kazuko Yoneshige, Azusa Ito, Akihiko Ueda, Yoji Kondo, Satoshi Nobumasa, Hitoshi Fujita, Yoshihiko Togashi, Yosuke Terashima, Masato De Velasco, Marco A Tomida, Shuta Nishio, Kazuto Springerplus Research We compared the performance of the 3D-Gene® mutation assay (3D-Gene® KRAS mutation assay kit) with the Scorpion-ARMS (therascreen® KRAS RGQ PCR Kit) and Luminex (MEBGEN™ KRAS kit) assays for the detection of KRAS mutations in formalin-fixed, paraffin-embedded tissue samples from 150 patients diagnosed with colorectal cancer. DNA was extracted from the paraffin-embedded tissue samples with or without macrodissection under hematoxylin and eosin staining and the KRAS mutation status was independently determined using these assays. Discordant results were re-analyzed by Sanger sequencing. Mutation detection analysis was successfully performed in all 150 specimens using the 3D-Gene® mutation assay without an invalid case. The concordance rate between the 3D-Gene® mutation assay and Scorpion-ARMS or Luminex was 98.7% (148/150). KRAS mutations were detected at a frequency of 35.3% (53/150) in colorectal cancer specimens. Three discrepant cases were found between the three assays. Overall, our results demonstrate a high concordance rate of between the 3D-Gene® mutation assay and the two existing in-vitro diagnostics kits. All three assays proved to be validated methods for detecting clinically significant KRAS mutations in paraffin-embedded tissue samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-4-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2015-01-05 /pmc/articles/PMC4320212/ /pubmed/25674493 http://dx.doi.org/10.1186/2193-1801-4-7 Text en © Sakai et al.; licensee Springer. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Sakai, Kazuko
Yoneshige, Azusa
Ito, Akihiko
Ueda, Yoji
Kondo, Satoshi
Nobumasa, Hitoshi
Fujita, Yoshihiko
Togashi, Yosuke
Terashima, Masato
De Velasco, Marco A
Tomida, Shuta
Nishio, Kazuto
Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
title Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
title_full Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
title_fullStr Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
title_full_unstemmed Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
title_short Performance of a novel KRAS mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
title_sort performance of a novel kras mutation assay for formalin-fixed paraffin embedded tissues of colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320212/
https://www.ncbi.nlm.nih.gov/pubmed/25674493
http://dx.doi.org/10.1186/2193-1801-4-7
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