Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer

Abstract The risk of developing metachronous gastric cancer (MGC) following curative endoscopic submucosal dissection (ESD) of early gastric cancer (EGC) remains even after eradicating Helicobacter pylori (HP) successfully. We screened initial EGC and adjacent non-cancerous mucosa ESD-resected speci...

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Autores principales: Kazuhiro Sakuta, Yu Sasaki, Yasuhiko Abe, Hidenori Sato, Masakuni Shoji, Takao Yaoita, Makoto Yagi, Naoko Mizumoto, Yusuke Onozato, Takashi Kon, Ayumi Koseki, Sonoko Sato, Ryoko Murakami, Yuki Miyano, Yoshiyuki Ueno
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Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/208876ad5a57449a9803c0d2a68fdd4b
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spelling oai:doaj.org-article:208876ad5a57449a9803c0d2a68fdd4b2021-12-02T13:58:11ZSomatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer10.1038/s41598-020-79195-02045-2322https://doaj.org/article/208876ad5a57449a9803c0d2a68fdd4b2020-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-79195-0https://doaj.org/toc/2045-2322Abstract The risk of developing metachronous gastric cancer (MGC) following curative endoscopic submucosal dissection (ESD) of early gastric cancer (EGC) remains even after eradicating Helicobacter pylori (HP) successfully. We screened initial EGC and adjacent non-cancerous mucosa ESD-resected specimens for somatic variants of 409 cancer-related genes, assessing their mutational burden (MB) to predict molecular markers for metachronous post-ESD development. We compared variants between ten patients diagnosed with MGC more than 3 years after ESD and ten age-matched patients who did not have MGC developments after successful HP eradication. We found no significant background differences between the two groups. In adjacent non-cancerous mucosa, the MB tended to be higher in the patients with metachronous developments than in the others. Somatic genomic alterations of RECQL4, JAK3, ARID1A, and MAGI1 genes were significantly associated with MGC development. The criteria including both the MB and their variants, which had potential significant values for predicting MGC. In conclusion, combined of assessing specific somatic variants and MB may be useful for predicting MGC development. This study included a limited number of subjects; however, our novel findings may encourage further exploration of the significance of the molecular features of EGC that predict MGC development, thereby promoting focused follow-up strategies and helping elucidate the mechanisms.Kazuhiro SakutaYu SasakiYasuhiko AbeHidenori SatoMasakuni ShojiTakao YaoitaMakoto YagiNaoko MizumotoYusuke OnozatoTakashi KonAyumi KosekiSonoko SatoRyoko MurakamiYuki MiyanoYoshiyuki UenoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Kazuhiro Sakuta
Yu Sasaki
Yasuhiko Abe
Hidenori Sato
Masakuni Shoji
Takao Yaoita
Makoto Yagi
Naoko Mizumoto
Yusuke Onozato
Takashi Kon
Ayumi Koseki
Sonoko Sato
Ryoko Murakami
Yuki Miyano
Yoshiyuki Ueno
Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
description Abstract The risk of developing metachronous gastric cancer (MGC) following curative endoscopic submucosal dissection (ESD) of early gastric cancer (EGC) remains even after eradicating Helicobacter pylori (HP) successfully. We screened initial EGC and adjacent non-cancerous mucosa ESD-resected specimens for somatic variants of 409 cancer-related genes, assessing their mutational burden (MB) to predict molecular markers for metachronous post-ESD development. We compared variants between ten patients diagnosed with MGC more than 3 years after ESD and ten age-matched patients who did not have MGC developments after successful HP eradication. We found no significant background differences between the two groups. In adjacent non-cancerous mucosa, the MB tended to be higher in the patients with metachronous developments than in the others. Somatic genomic alterations of RECQL4, JAK3, ARID1A, and MAGI1 genes were significantly associated with MGC development. The criteria including both the MB and their variants, which had potential significant values for predicting MGC. In conclusion, combined of assessing specific somatic variants and MB may be useful for predicting MGC development. This study included a limited number of subjects; however, our novel findings may encourage further exploration of the significance of the molecular features of EGC that predict MGC development, thereby promoting focused follow-up strategies and helping elucidate the mechanisms.
format article
author Kazuhiro Sakuta
Yu Sasaki
Yasuhiko Abe
Hidenori Sato
Masakuni Shoji
Takao Yaoita
Makoto Yagi
Naoko Mizumoto
Yusuke Onozato
Takashi Kon
Ayumi Koseki
Sonoko Sato
Ryoko Murakami
Yuki Miyano
Yoshiyuki Ueno
author_facet Kazuhiro Sakuta
Yu Sasaki
Yasuhiko Abe
Hidenori Sato
Masakuni Shoji
Takao Yaoita
Makoto Yagi
Naoko Mizumoto
Yusuke Onozato
Takashi Kon
Ayumi Koseki
Sonoko Sato
Ryoko Murakami
Yuki Miyano
Yoshiyuki Ueno
author_sort Kazuhiro Sakuta
title Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
title_short Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
title_full Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
title_fullStr Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
title_full_unstemmed Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
title_sort somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/208876ad5a57449a9803c0d2a68fdd4b
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