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Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis

Gastric cancer (GC) is one of the most wide-spread malignancies in the world. The oncogenic role of signaling of fibroblast growing factors (FGFs) and their receptors (FGFRs) in gastric tumorigenesis has been gradually elucidated by recent studies. The expression pattern and clinical correlations of...

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Autores principales: Zhang, Jinglin, Tang, Patrick M. K., Zhou, Yuhang, Cheng, Alfred S. L., Yu, Jun, Kang, Wei, To, Ka Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627225/
https://www.ncbi.nlm.nih.gov/pubmed/31242658
http://dx.doi.org/10.3390/cells8060637
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author Zhang, Jinglin
Tang, Patrick M. K.
Zhou, Yuhang
Cheng, Alfred S. L.
Yu, Jun
Kang, Wei
To, Ka Fai
author_facet Zhang, Jinglin
Tang, Patrick M. K.
Zhou, Yuhang
Cheng, Alfred S. L.
Yu, Jun
Kang, Wei
To, Ka Fai
author_sort Zhang, Jinglin
collection PubMed
description Gastric cancer (GC) is one of the most wide-spread malignancies in the world. The oncogenic role of signaling of fibroblast growing factors (FGFs) and their receptors (FGFRs) in gastric tumorigenesis has been gradually elucidated by recent studies. The expression pattern and clinical correlations of FGF and FGFR family members have been comprehensively delineated. Among them, FGF18 and FGFR2 demonstrate the most prominent driving role in gastric tumorigenesis with gene amplification or somatic mutations and serve as prognostic biomarkers. FGF-FGFR promotes tumor progression by crosstalking with multiple oncogenic pathways and this provides a rational therapeutic strategy by co-targeting the crosstalks to achieve synergistic effects. In this review, we comprehensively summarize the pathogenic mechanisms of FGF-FGFR signaling in gastric adenocarcinoma together with the current targeted strategies in aberrant FGF-FGFR activated GC cases.
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spelling pubmed-66272252019-07-23 Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis Zhang, Jinglin Tang, Patrick M. K. Zhou, Yuhang Cheng, Alfred S. L. Yu, Jun Kang, Wei To, Ka Fai Cells Review Gastric cancer (GC) is one of the most wide-spread malignancies in the world. The oncogenic role of signaling of fibroblast growing factors (FGFs) and their receptors (FGFRs) in gastric tumorigenesis has been gradually elucidated by recent studies. The expression pattern and clinical correlations of FGF and FGFR family members have been comprehensively delineated. Among them, FGF18 and FGFR2 demonstrate the most prominent driving role in gastric tumorigenesis with gene amplification or somatic mutations and serve as prognostic biomarkers. FGF-FGFR promotes tumor progression by crosstalking with multiple oncogenic pathways and this provides a rational therapeutic strategy by co-targeting the crosstalks to achieve synergistic effects. In this review, we comprehensively summarize the pathogenic mechanisms of FGF-FGFR signaling in gastric adenocarcinoma together with the current targeted strategies in aberrant FGF-FGFR activated GC cases. MDPI 2019-06-25 /pmc/articles/PMC6627225/ /pubmed/31242658 http://dx.doi.org/10.3390/cells8060637 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhang, Jinglin
Tang, Patrick M. K.
Zhou, Yuhang
Cheng, Alfred S. L.
Yu, Jun
Kang, Wei
To, Ka Fai
Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis
title Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis
title_full Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis
title_fullStr Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis
title_full_unstemmed Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis
title_short Targeting the Oncogenic FGF-FGFR Axis in Gastric Carcinogenesis
title_sort targeting the oncogenic fgf-fgfr axis in gastric carcinogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627225/
https://www.ncbi.nlm.nih.gov/pubmed/31242658
http://dx.doi.org/10.3390/cells8060637
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