Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/143536
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dc.creatorSousa, A
dc.creatorFerreira, M
dc.creatorOliveira, C
dc.creatorFerreira, PG
dc.date.accessioned2022-08-29T14:35:34Z-
dc.date.available2022-08-29T14:35:34Z-
dc.date.issued2020
dc.identifier.issn1664-8021
dc.identifier.urihttps://hdl.handle.net/10216/143536-
dc.description.abstractCancer has an important and considerable gender differential susceptibility confirmed by several epidemiological studies. Gastric (GC) and thyroid cancer (TC) are examples of malignancies with a higher incidence in males and females, respectively. Beyond environmental predisposing factors, it is expected that gender-specific gene deregulation contributes to this differential incidence. We performed a detailed characterization of the transcriptomic differences between genders in normal and tumor tissues from stomach and thyroid using Genotype-Tissue Expression (GTEx) and The Cancer Genome Atlas (TCGA) data. We found hundreds of sex-biased genes (SBGs). Most of the SBGs shared by normal and tumor belong to sexual chromosomes, while the normal and tumor-specific tend to be found in the autosomes. Expression of several cancer-associated genes is also found to differ between sexes in both types of tissue. Thousands of differentially expressed genes (DEGs) between paired tumor–normal tissues were identified in GC and TC. For both cancers, in the most susceptible gender, the DEGs were mostly under-expressed in the tumor tissue, with an enrichment for tumor-suppressor genes (TSGs). Moreover, we found gene networks preferentially associated to males in GC and to females in TC and correlated with cancer histological subtypes. Our results shed light on the molecular differences and commonalities between genders and provide novel insights in the differential risk underlying these cancers.
dc.description.sponsorshipThis work was supported by the FCT (Fundação para a Ciência e a Tecnologia) research grant IF/01127/2014, funded in the scope of the FCT Investigator Exploratory Project: “Understanding the impact of acquired and germline genetic variants in the complexity of gastric cancer”; FCT Ph.D. Studentship PD/BD/128007/2016; GenomePT project (reference 22184): “National Laboratory for Genome Sequencing and Analysis”; QREN L2 project (reference NORTE-01-0145- FEDER-000029): “Tumour secreted factors in EMT/non-EMT cells for invasion and metastization”; QREN L3 project (reference NORTE-01-0145-FEDER-000029): “Mapping genetic and phenotypic heterogeneity in HER2 positive cancers to anticipate and counteract resistance phenotypes”; 3D-ChroMe project (reference POCI-01-0145-FEDER-30164): “Solving the 3D chromatin structure of CDH1 locus to identify diseaseassociated mechanisms”; DOCnet project (reference NORTE01-0145-FEDER-000003): “Diabetes & obesity at the crossroads between Oncological and Cardiovascular diseases—A system analysis NETtwork towards precision medicine.”
dc.language.isoeng
dc.publisherFrontiers Media
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_NORTE/PD%2FBD%2F128007%2F2016/PT
dc.relation.ispartofFrontiers in Genetics, vol.11:808
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectdifferential expression
dc.subjectgastric cancer
dc.subjectgender differences
dc.subjectgene co-expression networks
dc.subjectGenotype-Tissue Expression
dc.subjectRNA-seq
dc.subjectThe Cancer Genome Atlas
dc.subjectthyroid cancer
dc.titleGender Differential Transcriptome in Gastric and Thyroid Cancers
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3389/fgene.2020.00808
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fgene.2020.00808/full
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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