Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells

The role of desmoglein-3 (DSG3) in oncogenesis is unclear. This study aimed to uncover molecular mechanisms through comparative transcriptome analysis in oral cancer cells, defining potential key genes and associated biological processes related to DSG3 expression. Four mRNA libraries of oral squamo...

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Main Authors: Hong Wan, Muy-Teck Teh, Giulia Mastroianni, Usama Sharif Ahmad
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/12/23/2710
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author Hong Wan
Muy-Teck Teh
Giulia Mastroianni
Usama Sharif Ahmad
author_facet Hong Wan
Muy-Teck Teh
Giulia Mastroianni
Usama Sharif Ahmad
author_sort Hong Wan
collection DOAJ
description The role of desmoglein-3 (DSG3) in oncogenesis is unclear. This study aimed to uncover molecular mechanisms through comparative transcriptome analysis in oral cancer cells, defining potential key genes and associated biological processes related to DSG3 expression. Four mRNA libraries of oral squamous carcinoma H413 cell lines were sequenced, and 599 candidate genes exhibited differential expression between DSG3-overexpressing and matched control lines, with 12 genes highly significantly differentially expressed, including 9 upregulated and 3 downregulated. Genes with known implications in cancer, such as MMP-13, KRT84, OLFM4, GJA1, AMOT and ADAMTS1, were strongly linked to DSG3 overexpression. Gene ontology analysis indicated that the DSG3-associated candidate gene products participate in crucial cellular processes such as junction assembly, focal adhesion, extracellular matrix formation, intermediate filament organisation and keratinocyte differentiation. Validation of RNA-Seq was performed through RT-qPCR, Western blotting and immunofluorescence analyses. Furthermore, using transmission electron microscopy, we meticulously examined desmosome morphology and revealed a slightly immature desmosome structure in DSG3-overexpressing cells compared to controls. No changes in desmosome frequency and diameter were observed between the two conditions. This study underscores intricate and multifaceted alterations associated with DSG3 in oral squamous carcinoma cells, implying a potential oncogenic role of this gene in biological processes that enable cell communication, motility and survival.
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spelling doaj.art-562663bbccff4092981e0868146986942023-12-08T15:13:07ZengMDPI AGCells2073-44092023-11-011223271010.3390/cells12232710Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer CellsHong Wan0Muy-Teck Teh1Giulia Mastroianni2Usama Sharif Ahmad3Center for Immunobiology and Regenerative Medicine, Institute of Dentistry, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UKCenter for Immunobiology and Regenerative Medicine, Institute of Dentistry, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UKSchool of Biological and Behavioural Sciences, Faculty of Science and Engineering, Queen Mary University of London, London E1 4NS, UKCenter for Immunobiology and Regenerative Medicine, Institute of Dentistry, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UKThe role of desmoglein-3 (DSG3) in oncogenesis is unclear. This study aimed to uncover molecular mechanisms through comparative transcriptome analysis in oral cancer cells, defining potential key genes and associated biological processes related to DSG3 expression. Four mRNA libraries of oral squamous carcinoma H413 cell lines were sequenced, and 599 candidate genes exhibited differential expression between DSG3-overexpressing and matched control lines, with 12 genes highly significantly differentially expressed, including 9 upregulated and 3 downregulated. Genes with known implications in cancer, such as MMP-13, KRT84, OLFM4, GJA1, AMOT and ADAMTS1, were strongly linked to DSG3 overexpression. Gene ontology analysis indicated that the DSG3-associated candidate gene products participate in crucial cellular processes such as junction assembly, focal adhesion, extracellular matrix formation, intermediate filament organisation and keratinocyte differentiation. Validation of RNA-Seq was performed through RT-qPCR, Western blotting and immunofluorescence analyses. Furthermore, using transmission electron microscopy, we meticulously examined desmosome morphology and revealed a slightly immature desmosome structure in DSG3-overexpressing cells compared to controls. No changes in desmosome frequency and diameter were observed between the two conditions. This study underscores intricate and multifaceted alterations associated with DSG3 in oral squamous carcinoma cells, implying a potential oncogenic role of this gene in biological processes that enable cell communication, motility and survival.https://www.mdpi.com/2073-4409/12/23/2710desmoglein-3oral squamous carcinoma cellsRNA-Seqbioinformaticstransmission electron microscopydesmosomes
spellingShingle Hong Wan
Muy-Teck Teh
Giulia Mastroianni
Usama Sharif Ahmad
Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells
Cells
desmoglein-3
oral squamous carcinoma cells
RNA-Seq
bioinformatics
transmission electron microscopy
desmosomes
title Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells
title_full Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells
title_fullStr Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells
title_full_unstemmed Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells
title_short Comparative Transcriptome Analysis Identifies Desmoglein-3 as a Potential Oncogene in Oral Cancer Cells
title_sort comparative transcriptome analysis identifies desmoglein 3 as a potential oncogene in oral cancer cells
topic desmoglein-3
oral squamous carcinoma cells
RNA-Seq
bioinformatics
transmission electron microscopy
desmosomes
url https://www.mdpi.com/2073-4409/12/23/2710
work_keys_str_mv AT hongwan comparativetranscriptomeanalysisidentifiesdesmoglein3asapotentialoncogeneinoralcancercells
AT muyteckteh comparativetranscriptomeanalysisidentifiesdesmoglein3asapotentialoncogeneinoralcancercells
AT giuliamastroianni comparativetranscriptomeanalysisidentifiesdesmoglein3asapotentialoncogeneinoralcancercells
AT usamasharifahmad comparativetranscriptomeanalysisidentifiesdesmoglein3asapotentialoncogeneinoralcancercells