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Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors

BACKGROUND AND AIM: The mechanism underlying carcinogenesis and the genomic features of superficial non‐ampullary duodenal epithelial tumors (SNADETs) have not been elucidated in detail. In this study, we examined the genomic features of incipient SNADETs, such as small lesions resected via endoscop...

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Autores principales: Miyamoto, Shuichi, Suda, Goki, Ishikawa, Marin, Hayashi, Hideyuki, Nimura, Satoshi, Matsuno, Yoshihiro, Mori, Ryo, Tanishima, Shigeki, Kudo, Takahiko, Takagi, Tomofumi, Yamamoto, Yoshiya, Ono, Shoko, Shimizu, Yuichi, Sakamoto, Naoya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454473/
https://www.ncbi.nlm.nih.gov/pubmed/34584977
http://dx.doi.org/10.1002/jgh3.12632
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author Miyamoto, Shuichi
Suda, Goki
Ishikawa, Marin
Hayashi, Hideyuki
Nimura, Satoshi
Matsuno, Yoshihiro
Mori, Ryo
Tanishima, Shigeki
Kudo, Takahiko
Takagi, Tomofumi
Yamamoto, Yoshiya
Ono, Shoko
Shimizu, Yuichi
Sakamoto, Naoya
author_facet Miyamoto, Shuichi
Suda, Goki
Ishikawa, Marin
Hayashi, Hideyuki
Nimura, Satoshi
Matsuno, Yoshihiro
Mori, Ryo
Tanishima, Shigeki
Kudo, Takahiko
Takagi, Tomofumi
Yamamoto, Yoshiya
Ono, Shoko
Shimizu, Yuichi
Sakamoto, Naoya
author_sort Miyamoto, Shuichi
collection PubMed
description BACKGROUND AND AIM: The mechanism underlying carcinogenesis and the genomic features of superficial non‐ampullary duodenal epithelial tumors (SNADETs) have not been elucidated in detail. In this study, we examined the genomic features of incipient SNADETs, such as small lesions resected via endoscopic treatment, using next‐generation sequencing (NGS). METHODS: Twenty consecutive patients who underwent endoscopic treatment for SNADETs of less than 20 mm between January and December 2017 were enrolled. Targeted genomic sequencing was performed through NGS using a panel of 160 cancer‐related genes. Furthermore, the alteration/mutation frequencies in SNADETs were examined. RESULTS: The maximum size of the SNADETs examined in this study was 12 mm in diameter. Five SNADETs were classified as low‐grade dysplasia (LGD) tumors, while 14 SNADETs were classified as high‐grade dysplasia tumors. Only one carcinoma in situ was detected. NGS data for 16 samples were obtained. APC alterations were detected in 81% of samples (13/16). KRAS, BRAF, and TP53 alterations were detected in 25% (4/16), 18.8% (3/16), and 6.3% (1/16) of cases, respectively. CONCLUSION: We detected APC alterations in most small SNADETs resected via endoscopic treatment, from LGD to carcinoma samples. Even in SNADETs classified as small LGD exhibited KRAS and BRAF alterations.
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spelling pubmed-84544732021-09-27 Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors Miyamoto, Shuichi Suda, Goki Ishikawa, Marin Hayashi, Hideyuki Nimura, Satoshi Matsuno, Yoshihiro Mori, Ryo Tanishima, Shigeki Kudo, Takahiko Takagi, Tomofumi Yamamoto, Yoshiya Ono, Shoko Shimizu, Yuichi Sakamoto, Naoya JGH Open Original Articles BACKGROUND AND AIM: The mechanism underlying carcinogenesis and the genomic features of superficial non‐ampullary duodenal epithelial tumors (SNADETs) have not been elucidated in detail. In this study, we examined the genomic features of incipient SNADETs, such as small lesions resected via endoscopic treatment, using next‐generation sequencing (NGS). METHODS: Twenty consecutive patients who underwent endoscopic treatment for SNADETs of less than 20 mm between January and December 2017 were enrolled. Targeted genomic sequencing was performed through NGS using a panel of 160 cancer‐related genes. Furthermore, the alteration/mutation frequencies in SNADETs were examined. RESULTS: The maximum size of the SNADETs examined in this study was 12 mm in diameter. Five SNADETs were classified as low‐grade dysplasia (LGD) tumors, while 14 SNADETs were classified as high‐grade dysplasia tumors. Only one carcinoma in situ was detected. NGS data for 16 samples were obtained. APC alterations were detected in 81% of samples (13/16). KRAS, BRAF, and TP53 alterations were detected in 25% (4/16), 18.8% (3/16), and 6.3% (1/16) of cases, respectively. CONCLUSION: We detected APC alterations in most small SNADETs resected via endoscopic treatment, from LGD to carcinoma samples. Even in SNADETs classified as small LGD exhibited KRAS and BRAF alterations. Wiley Publishing Asia Pty Ltd 2021-08-03 /pmc/articles/PMC8454473/ /pubmed/34584977 http://dx.doi.org/10.1002/jgh3.12632 Text en © 2021 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Miyamoto, Shuichi
Suda, Goki
Ishikawa, Marin
Hayashi, Hideyuki
Nimura, Satoshi
Matsuno, Yoshihiro
Mori, Ryo
Tanishima, Shigeki
Kudo, Takahiko
Takagi, Tomofumi
Yamamoto, Yoshiya
Ono, Shoko
Shimizu, Yuichi
Sakamoto, Naoya
Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
title Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
title_full Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
title_fullStr Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
title_full_unstemmed Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
title_short Genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
title_sort genomic profiling of intestinal/mixed‐type superficial non‐ampullary duodenal epithelial tumors
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454473/
https://www.ncbi.nlm.nih.gov/pubmed/34584977
http://dx.doi.org/10.1002/jgh3.12632
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