Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer

Abstract Fibroblast growth factor receptor 2 (FGFR2) has two isoforms: IIIb type and IIIc type. Clinicopathologic significance of these two FGFR2 subtypes in gastric cancer remains to be known. This study aimed to clarify the clinicopathologic difference of FGFR2IIIb and/or FGFR2IIIc overexpression....

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Autores principales: Masakazu Yashiro, Kenji Kuroda, Go Masuda, Tomohisa Okuno, Yuichiro Miki, Yurie Yamamoto, Tomohiro Sera, Atsushi Sugimoto, Shuhei Kushiyama, Sadaaki Nishimura, Shingo Togano, Masaichi Ohira
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/57f653c36cdc4e4f86e8dfd190fdd59e
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spelling oai:doaj.org-article:57f653c36cdc4e4f86e8dfd190fdd59e2021-12-02T13:20:12ZClinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer10.1038/s41598-021-84107-x2045-2322https://doaj.org/article/57f653c36cdc4e4f86e8dfd190fdd59e2021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-84107-xhttps://doaj.org/toc/2045-2322Abstract Fibroblast growth factor receptor 2 (FGFR2) has two isoforms: IIIb type and IIIc type. Clinicopathologic significance of these two FGFR2 subtypes in gastric cancer remains to be known. This study aimed to clarify the clinicopathologic difference of FGFR2IIIb and/or FGFR2IIIc overexpression. A total of 562 patients who underwent gastrectomy was enrolled. The expressions of FGFR2IIIb and FGFR2IIIc were retrospectively examined by immunohistochemistry or fluorescence in situ hybridization (FISH) using the 562 gastric tumors. We evaluated the correlation between clinicopathologic features and FGFR2IIIb overexpression and/or FGFR2IIIc overexpression in gastric cancer. FGFR2IIIb overexpression was observed in 28 cases (4.9%), and FGFR2IIIc overexpression was observed in four cases (0.7%). All four FGFR2IIIc cases were also positive for FGFR2IIIb, but not in the same cancer cells. FGFR2IIIb and/or FGFR2IIIc overexpression was significantly correlated with lymph node metastasis and clinical stage. Both FGFR2IIIb and FGFR2IIIc were significantly associated with poor overall survival. A multivariate analysis showed that FGFR2IIIc expression was significantly correlated with overall survival. FISH analysis indicated that FGFR2 amplification was correlated with FGFR2IIIb and/or FGFR2IIIc overexpression. These findings suggested that gastric tumor overexpressed FGFR2IIIc and/or FGFR2IIIb at the frequency of 4.9%. FGFR2IIIc overexpression might be independent prognostic factor for patients with gastric cancer.Masakazu YashiroKenji KurodaGo MasudaTomohisa OkunoYuichiro MikiYurie YamamotoTomohiro SeraAtsushi SugimotoShuhei KushiyamaSadaaki NishimuraShingo ToganoMasaichi OhiraNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Masakazu Yashiro
Kenji Kuroda
Go Masuda
Tomohisa Okuno
Yuichiro Miki
Yurie Yamamoto
Tomohiro Sera
Atsushi Sugimoto
Shuhei Kushiyama
Sadaaki Nishimura
Shingo Togano
Masaichi Ohira
Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer
description Abstract Fibroblast growth factor receptor 2 (FGFR2) has two isoforms: IIIb type and IIIc type. Clinicopathologic significance of these two FGFR2 subtypes in gastric cancer remains to be known. This study aimed to clarify the clinicopathologic difference of FGFR2IIIb and/or FGFR2IIIc overexpression. A total of 562 patients who underwent gastrectomy was enrolled. The expressions of FGFR2IIIb and FGFR2IIIc were retrospectively examined by immunohistochemistry or fluorescence in situ hybridization (FISH) using the 562 gastric tumors. We evaluated the correlation between clinicopathologic features and FGFR2IIIb overexpression and/or FGFR2IIIc overexpression in gastric cancer. FGFR2IIIb overexpression was observed in 28 cases (4.9%), and FGFR2IIIc overexpression was observed in four cases (0.7%). All four FGFR2IIIc cases were also positive for FGFR2IIIb, but not in the same cancer cells. FGFR2IIIb and/or FGFR2IIIc overexpression was significantly correlated with lymph node metastasis and clinical stage. Both FGFR2IIIb and FGFR2IIIc were significantly associated with poor overall survival. A multivariate analysis showed that FGFR2IIIc expression was significantly correlated with overall survival. FISH analysis indicated that FGFR2 amplification was correlated with FGFR2IIIb and/or FGFR2IIIc overexpression. These findings suggested that gastric tumor overexpressed FGFR2IIIc and/or FGFR2IIIb at the frequency of 4.9%. FGFR2IIIc overexpression might be independent prognostic factor for patients with gastric cancer.
format article
author Masakazu Yashiro
Kenji Kuroda
Go Masuda
Tomohisa Okuno
Yuichiro Miki
Yurie Yamamoto
Tomohiro Sera
Atsushi Sugimoto
Shuhei Kushiyama
Sadaaki Nishimura
Shingo Togano
Masaichi Ohira
author_facet Masakazu Yashiro
Kenji Kuroda
Go Masuda
Tomohisa Okuno
Yuichiro Miki
Yurie Yamamoto
Tomohiro Sera
Atsushi Sugimoto
Shuhei Kushiyama
Sadaaki Nishimura
Shingo Togano
Masaichi Ohira
author_sort Masakazu Yashiro
title Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer
title_short Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer
title_full Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer
title_fullStr Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer
title_full_unstemmed Clinical difference between fibroblast growth factor receptor 2 subclass, type IIIb and type IIIc, in gastric cancer
title_sort clinical difference between fibroblast growth factor receptor 2 subclass, type iiib and type iiic, in gastric cancer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/57f653c36cdc4e4f86e8dfd190fdd59e
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