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NTRK fusion in Japanese colorectal adenocarcinomas
NTRK fusion-positive tumors are known to be highly sensitive to TRK inhibitors, such as larotrectinib and entrectinib. Therefore, identification of patients who can potentially benefit from these inhibitors is important; however, the frequency of NTRK fusions in Japanese patients with colorectal can...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952565/ https://www.ncbi.nlm.nih.gov/pubmed/33707574 http://dx.doi.org/10.1038/s41598-021-85075-y |
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author | Yamashiro, Yuya Kurihara, Taisei Hayashi, Takuo Suehara, Yoshiyuki Yao, Takashi Kato, Shunsuke Saito, Tsuyoshi |
author_facet | Yamashiro, Yuya Kurihara, Taisei Hayashi, Takuo Suehara, Yoshiyuki Yao, Takashi Kato, Shunsuke Saito, Tsuyoshi |
author_sort | Yamashiro, Yuya |
collection | PubMed |
description | NTRK fusion-positive tumors are known to be highly sensitive to TRK inhibitors, such as larotrectinib and entrectinib. Therefore, identification of patients who can potentially benefit from these inhibitors is important; however, the frequency of NTRK fusions in Japanese patients with colorectal cancer (CRC) is unknown. We performed pan-TRK staining using TMA-based immunohistochemistry (IHC) on samples from 971 consecutive Japanese CRC cases from a single institution. Positive cases were further analyzed using NanoString and subsequent targeted RNA sequencing. We found three positive cases using TRK-IHC. Furthermore, the Nanostring assay supported the presence of NTRK fusion in these cases. Subsequent targeted RNA-sequencing and RT-PCR revealed two cases with TPM3-NTRK1 and one with TPR-NTRK1. The TNM stages of these cases were stage I, stage IIA, and stage IIIB, and two showed microsatellite instability-high status. Next-generation sequencing analysis using Cancer hotspot panel revealed TP53 and SMAD4 mutations in separate cases. IHC of β-catenin did not show nuclear accumulation. We found three cases (0.31%) of CRC with NTRK1 fusion among 971 consecutive Japanese CRC cases. No potential driver alterations other than NTRK fusion were identified in these three patients. |
format | Online Article Text |
id | pubmed-7952565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79525652021-03-12 NTRK fusion in Japanese colorectal adenocarcinomas Yamashiro, Yuya Kurihara, Taisei Hayashi, Takuo Suehara, Yoshiyuki Yao, Takashi Kato, Shunsuke Saito, Tsuyoshi Sci Rep Article NTRK fusion-positive tumors are known to be highly sensitive to TRK inhibitors, such as larotrectinib and entrectinib. Therefore, identification of patients who can potentially benefit from these inhibitors is important; however, the frequency of NTRK fusions in Japanese patients with colorectal cancer (CRC) is unknown. We performed pan-TRK staining using TMA-based immunohistochemistry (IHC) on samples from 971 consecutive Japanese CRC cases from a single institution. Positive cases were further analyzed using NanoString and subsequent targeted RNA sequencing. We found three positive cases using TRK-IHC. Furthermore, the Nanostring assay supported the presence of NTRK fusion in these cases. Subsequent targeted RNA-sequencing and RT-PCR revealed two cases with TPM3-NTRK1 and one with TPR-NTRK1. The TNM stages of these cases were stage I, stage IIA, and stage IIIB, and two showed microsatellite instability-high status. Next-generation sequencing analysis using Cancer hotspot panel revealed TP53 and SMAD4 mutations in separate cases. IHC of β-catenin did not show nuclear accumulation. We found three cases (0.31%) of CRC with NTRK1 fusion among 971 consecutive Japanese CRC cases. No potential driver alterations other than NTRK fusion were identified in these three patients. Nature Publishing Group UK 2021-03-11 /pmc/articles/PMC7952565/ /pubmed/33707574 http://dx.doi.org/10.1038/s41598-021-85075-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yamashiro, Yuya Kurihara, Taisei Hayashi, Takuo Suehara, Yoshiyuki Yao, Takashi Kato, Shunsuke Saito, Tsuyoshi NTRK fusion in Japanese colorectal adenocarcinomas |
title | NTRK fusion in Japanese colorectal adenocarcinomas |
title_full | NTRK fusion in Japanese colorectal adenocarcinomas |
title_fullStr | NTRK fusion in Japanese colorectal adenocarcinomas |
title_full_unstemmed | NTRK fusion in Japanese colorectal adenocarcinomas |
title_short | NTRK fusion in Japanese colorectal adenocarcinomas |
title_sort | ntrk fusion in japanese colorectal adenocarcinomas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952565/ https://www.ncbi.nlm.nih.gov/pubmed/33707574 http://dx.doi.org/10.1038/s41598-021-85075-y |
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