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A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors

OBJECTIVE: We performed a pan-cancer analysis to explore the potential mechanisms of FAT4 in 33 different tumors. METHODS: In this study, we selected 33 types of cancers based on the datasets of TCGA (the cancer genome atlas). We analyzed the expression of FAT4 in tumor and normal tissues. Meanwhile...

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Autores principales: Mao, Weili, Zhou, Jiajing, Hu, Jie, Zhao, Kui, Fu, Zhenling, Wang, Jun, Mao, Kaili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424548/
https://www.ncbi.nlm.nih.gov/pubmed/36051999
http://dx.doi.org/10.3389/fpubh.2022.969070
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author Mao, Weili
Zhou, Jiajing
Hu, Jie
Zhao, Kui
Fu, Zhenling
Wang, Jun
Mao, Kaili
author_facet Mao, Weili
Zhou, Jiajing
Hu, Jie
Zhao, Kui
Fu, Zhenling
Wang, Jun
Mao, Kaili
author_sort Mao, Weili
collection PubMed
description OBJECTIVE: We performed a pan-cancer analysis to explore the potential mechanisms of FAT4 in 33 different tumors. METHODS: In this study, we selected 33 types of cancers based on the datasets of TCGA (the cancer genome atlas). We analyzed the expression of FAT4 in tumor and normal tissues. Meanwhile, we analyzed the expression levels of FAT4 in tissues from tumors of different stages. Kaplan-Meier survival analysis, Tumor Mutational Burden (TMB), Microsatellite Instability (MSI), immune infiltration analysis, Gene set enrichment analysis (GSEA), and FAT4-related gene enrichment analysis were performed. RESULTS: FAT4 expression in most tumor tissues was lower than in corresponding control tissues. FAT4 expression was different in different stages of bladder cancer (BLCA), kidney clear cell carcinoma (KIRC), and breast cancer (BRCA). In addition, the expression level of FAT4 in different types of tumors has an important impact on the prognosis of patients. FAT4 might influence the efficacy of immunotherapy via tumor burden and microsatellite instability. We observed a statistically positive correlation between cancer-associated fibroblasts and FAT4 expression in most tumors. GSEA of BLCA indicated that low FAT4 expression groups were mainly enriched in calcium signaling pathway and chemokine signaling pathway. GSEA analysis of KIRC suggested low FAT4 expression groups were mainly involved in olfactory transduction and oxidative phosphorylation. Kyoto Encyclopedia of Genes and Genomes (KEGG) indicated that the role of FAT4 in the pathogenesis of cancer may be related to human papillomavirus infection, Hippo signaling pathway, PI3K–Akt signaling pathway, etc. Gene Ontology (GO) enrichment analysis further showed that most of these genes were related to the pathways or cell biology, such as peptidyl–tyrosine phosphorylation, cell junction assembly, protein tyrosine kinase activity, etc. CONCLUSION: Our study summarized and analyzed the antitumor effect of FAT4 in different tumors comprehensively, which aided in understanding the role of FAT4 in tumorigenesis from the perspective of clinical tumor samples. Pan-cancer analysis showed that FAT4 to be novel biomarkers for various cancers prognosis.
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spelling pubmed-94245482022-08-31 A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors Mao, Weili Zhou, Jiajing Hu, Jie Zhao, Kui Fu, Zhenling Wang, Jun Mao, Kaili Front Public Health Public Health OBJECTIVE: We performed a pan-cancer analysis to explore the potential mechanisms of FAT4 in 33 different tumors. METHODS: In this study, we selected 33 types of cancers based on the datasets of TCGA (the cancer genome atlas). We analyzed the expression of FAT4 in tumor and normal tissues. Meanwhile, we analyzed the expression levels of FAT4 in tissues from tumors of different stages. Kaplan-Meier survival analysis, Tumor Mutational Burden (TMB), Microsatellite Instability (MSI), immune infiltration analysis, Gene set enrichment analysis (GSEA), and FAT4-related gene enrichment analysis were performed. RESULTS: FAT4 expression in most tumor tissues was lower than in corresponding control tissues. FAT4 expression was different in different stages of bladder cancer (BLCA), kidney clear cell carcinoma (KIRC), and breast cancer (BRCA). In addition, the expression level of FAT4 in different types of tumors has an important impact on the prognosis of patients. FAT4 might influence the efficacy of immunotherapy via tumor burden and microsatellite instability. We observed a statistically positive correlation between cancer-associated fibroblasts and FAT4 expression in most tumors. GSEA of BLCA indicated that low FAT4 expression groups were mainly enriched in calcium signaling pathway and chemokine signaling pathway. GSEA analysis of KIRC suggested low FAT4 expression groups were mainly involved in olfactory transduction and oxidative phosphorylation. Kyoto Encyclopedia of Genes and Genomes (KEGG) indicated that the role of FAT4 in the pathogenesis of cancer may be related to human papillomavirus infection, Hippo signaling pathway, PI3K–Akt signaling pathway, etc. Gene Ontology (GO) enrichment analysis further showed that most of these genes were related to the pathways or cell biology, such as peptidyl–tyrosine phosphorylation, cell junction assembly, protein tyrosine kinase activity, etc. CONCLUSION: Our study summarized and analyzed the antitumor effect of FAT4 in different tumors comprehensively, which aided in understanding the role of FAT4 in tumorigenesis from the perspective of clinical tumor samples. Pan-cancer analysis showed that FAT4 to be novel biomarkers for various cancers prognosis. Frontiers Media S.A. 2022-08-16 /pmc/articles/PMC9424548/ /pubmed/36051999 http://dx.doi.org/10.3389/fpubh.2022.969070 Text en Copyright © 2022 Mao, Zhou, Hu, Zhao, Fu, Wang and Mao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Mao, Weili
Zhou, Jiajing
Hu, Jie
Zhao, Kui
Fu, Zhenling
Wang, Jun
Mao, Kaili
A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors
title A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors
title_full A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors
title_fullStr A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors
title_full_unstemmed A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors
title_short A pan-cancer analysis of FAT atypical cadherin 4 (FAT4) in human tumors
title_sort pan-cancer analysis of fat atypical cadherin 4 (fat4) in human tumors
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424548/
https://www.ncbi.nlm.nih.gov/pubmed/36051999
http://dx.doi.org/10.3389/fpubh.2022.969070
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