Cargando…

Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker

Background: The family with sequence similarity 83 member D (FAM83D) protein is known to play a significant role in many human diseases. However, its role in cancer remains ambiguous. This study aimed to investigate the function of FAM83D in a pan-cancer analysis, with a special focus on breast canc...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Haiyang, Chen, Qinhao, Wang, Ziming, Qian, Xiaojun, Pan, Yueyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780495/
https://www.ncbi.nlm.nih.gov/pubmed/36568373
http://dx.doi.org/10.3389/fgene.2022.1009325
_version_ 1784856852456013824
author Yu, Haiyang
Chen, Qinhao
Wang, Ziming
Qian, Xiaojun
Pan, Yueyin
author_facet Yu, Haiyang
Chen, Qinhao
Wang, Ziming
Qian, Xiaojun
Pan, Yueyin
author_sort Yu, Haiyang
collection PubMed
description Background: The family with sequence similarity 83 member D (FAM83D) protein is known to play a significant role in many human diseases. However, its role in cancer remains ambiguous. This study aimed to investigate the function of FAM83D in a pan-cancer analysis, with a special focus on breast cancer. Methods: Samples were collected from The Cancer Genome Atlas (TCGA) and used for bioinformatic analysis. Datasets from the Gene Expression Omnibus (GEO) and Genotype-Tissue Expression (GTEx) databases were also analyzed for verification. The potential value of FAM83D as a prognostic and diagnostic biomarker was visualized through R software. The “survival” and “GSVA” package were used for univariate, multivariate and pathway enrichment analyseis. We further analyzed the CancerSEA databases and TISIDB websites for single-cell and immune-related profiling. Lastly, we validated those data in vitro using quantitative reverse transcriptase-polymerase chain reaction (RT‒qPCR), cell counting kit-8 (CCK-8), transwell, flow cytometry, and tumorigenicity assays in a murine cell line model. Results: The expression of FAM83D in tumor samples was significantly higher than in normal tissues for most cancer types in the datasets. We confirmed this finding using RT‒qPCR in a breast cancer cell line. Analysis of multiple datasets suggests that overall survival (OS) was extremely poor for breast cancer patients with high FAM83D expression. The CCK-8 assay demonstrated that MCF-7 cell proliferation was inhibited after genetic silencing of FAM83D. Transwell assay showed that knockdown of FAM83D significantly inhibited the invasion and migration ability of MCF-7 cells compared to the control. The results of flow cytometry showed that silencing FAM83D could block the G1 phase of MCF-7 cells compared with negative groups. The tumorigenicity assay in nude mice indicated that the tumorigenic ability to silence FAM83D decreased compared. Conclusion: Results suggest that FAM83D expression can serve as a valuable biomarker and core gene across cancer types. Furthermore, FAM83D expression is significantly associated with MCF-7 cell proliferation and thus may be a prospective prognostic biomarker especially for breast cancer.
format Online
Article
Text
id pubmed-9780495
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-97804952022-12-24 Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker Yu, Haiyang Chen, Qinhao Wang, Ziming Qian, Xiaojun Pan, Yueyin Front Genet Genetics Background: The family with sequence similarity 83 member D (FAM83D) protein is known to play a significant role in many human diseases. However, its role in cancer remains ambiguous. This study aimed to investigate the function of FAM83D in a pan-cancer analysis, with a special focus on breast cancer. Methods: Samples were collected from The Cancer Genome Atlas (TCGA) and used for bioinformatic analysis. Datasets from the Gene Expression Omnibus (GEO) and Genotype-Tissue Expression (GTEx) databases were also analyzed for verification. The potential value of FAM83D as a prognostic and diagnostic biomarker was visualized through R software. The “survival” and “GSVA” package were used for univariate, multivariate and pathway enrichment analyseis. We further analyzed the CancerSEA databases and TISIDB websites for single-cell and immune-related profiling. Lastly, we validated those data in vitro using quantitative reverse transcriptase-polymerase chain reaction (RT‒qPCR), cell counting kit-8 (CCK-8), transwell, flow cytometry, and tumorigenicity assays in a murine cell line model. Results: The expression of FAM83D in tumor samples was significantly higher than in normal tissues for most cancer types in the datasets. We confirmed this finding using RT‒qPCR in a breast cancer cell line. Analysis of multiple datasets suggests that overall survival (OS) was extremely poor for breast cancer patients with high FAM83D expression. The CCK-8 assay demonstrated that MCF-7 cell proliferation was inhibited after genetic silencing of FAM83D. Transwell assay showed that knockdown of FAM83D significantly inhibited the invasion and migration ability of MCF-7 cells compared to the control. The results of flow cytometry showed that silencing FAM83D could block the G1 phase of MCF-7 cells compared with negative groups. The tumorigenicity assay in nude mice indicated that the tumorigenic ability to silence FAM83D decreased compared. Conclusion: Results suggest that FAM83D expression can serve as a valuable biomarker and core gene across cancer types. Furthermore, FAM83D expression is significantly associated with MCF-7 cell proliferation and thus may be a prospective prognostic biomarker especially for breast cancer. Frontiers Media S.A. 2022-12-09 /pmc/articles/PMC9780495/ /pubmed/36568373 http://dx.doi.org/10.3389/fgene.2022.1009325 Text en Copyright © 2022 Yu, Chen, Wang, Qian and Pan. 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 Genetics
Yu, Haiyang
Chen, Qinhao
Wang, Ziming
Qian, Xiaojun
Pan, Yueyin
Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker
title Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker
title_full Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker
title_fullStr Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker
title_full_unstemmed Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker
title_short Pan-cancer and single-cell analysis reveals FAM83D expression as a cancer prognostic biomarker
title_sort pan-cancer and single-cell analysis reveals fam83d expression as a cancer prognostic biomarker
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780495/
https://www.ncbi.nlm.nih.gov/pubmed/36568373
http://dx.doi.org/10.3389/fgene.2022.1009325
work_keys_str_mv AT yuhaiyang pancancerandsinglecellanalysisrevealsfam83dexpressionasacancerprognosticbiomarker
AT chenqinhao pancancerandsinglecellanalysisrevealsfam83dexpressionasacancerprognosticbiomarker
AT wangziming pancancerandsinglecellanalysisrevealsfam83dexpressionasacancerprognosticbiomarker
AT qianxiaojun pancancerandsinglecellanalysisrevealsfam83dexpressionasacancerprognosticbiomarker
AT panyueyin pancancerandsinglecellanalysisrevealsfam83dexpressionasacancerprognosticbiomarker