HLA-G 14 bp In/Del and +3142 C/G genotypes are differentially expressed between patients with grade IV gliomas and controls
| dc.creator | Kênia Cristina S.f.de Magalhães | |
| dc.creator | Eduardo a. Donadi | |
| dc.creator | Istéfani Luciene da Silva | |
| dc.creator | Renata t. Simões | |
| dc.creator | Karla r. Silva | |
| dc.creator | Nathália a. Gomes | |
| dc.creator | Ibrahim Sadissou | |
| dc.creator | Gérvasio t. Carvalho | |
| dc.creator | Marcelo a. Buzellin | |
| dc.creator | Luciene s. Tafuri | |
| dc.creator | Cristiana Buzelin Nunes | |
| dc.creator | Maurício b. Nunes | |
| dc.date.accessioned | 2023-05-15T19:22:47Z | |
| dc.date.accessioned | 2025-09-09T01:30:33Z | |
| dc.date.available | 2023-05-15T19:22:47Z | |
| dc.date.issued | 2021 | |
| dc.format.mimetype | ||
| dc.identifier.doi | 10.1080/00207454.2020.1744593 | |
| dc.identifier.issn | 00207454 | |
| dc.identifier.uri | https://hdl.handle.net/1843/53385 | |
| dc.language | eng | |
| dc.publisher | Universidade Federal de Minas Gerais | |
| dc.relation.ispartof | International Journal of Neuroscience | |
| dc.rights | Acesso Restrito | |
| dc.subject | Neoplasias Encefálicas | |
| dc.subject | Glioma | |
| dc.subject.other | Brain tumors | |
| dc.subject.other | GBM | |
| dc.subject.other | HLA-G polymorphism | |
| dc.subject.other | 3' UTR; | |
| dc.subject.other | Plasma expression | |
| dc.title | HLA-G 14 bp In/Del and +3142 C/G genotypes are differentially expressed between patients with grade IV gliomas and controls | |
| dc.type | Artigo de periódico | |
| local.citation.epage | 335 | |
| local.citation.issue | 4 | |
| local.citation.spage | 327 | |
| local.citation.volume | 131 | |
| local.description.resumo | Aim: Human Leukocyte Antigen-G (HLA-G) is a non-classical class I molecule that is involved in maternal–fetal immunotolerance. In cancer, this molecule contributes to the tumor escape. The aim of this study was to evaluate the 14 bp In/Del and þ3142 C > G polymorphisms of the HLAG 30 UTR and its relation with plasma and tissue HLA-G expression in patients with grade IV (high-grade) and grade I/II (low-grade) gliomas and controls. Patients and methods: Peripheral blood and tumor biopsies were collected from 85 patients with gliomas and blood samples from 94 controls. Polymorphisms were analyzed from blood DNA. Soluble HLA-G (sHLA-G) was measured by ELISA in plasma of the subjects and the tissue expression by immunohistochemistry on patient’s tissue. Results: Higher levels of sHLA-G were observed in grade IV gliomas patients than in controls (p < 0.0001). In grade IV patients, the heterozygous 14pb In/Del, þ3142 C/G genotypes and Del/C In/G haplotype were associated with higher sHLA-G levels (p < 0.0001) when compared with controls. GBM patients were stratified into high and low sHLA-G expression and an association was found between þ3142 C allele and high sHLA-G plasmatic levels (p ¼ 0.0095). Tissue HLA-G immunolabel was higher in high-grade than low-grade gliomas (p ¼ 0.0033). Conclusion: This was the first study evaluating HLA-G 30 UTR polymorphisms and expression in patients with gliomas. The 14 bp In/Del and þ3142 C/G genotypes and haplotypes showed high influence over sHLA-G expression, suggesting a heterozygous advantage in the tumor context and may contribute to a worse prognosis in glioma patients. | |
| local.identifier.orcid | https://orcid.org/0000-0002-5266-6870 | |
| local.publisher.country | Brasil | |
| local.publisher.department | MED - DEPARTAMENTO DE ANATOMIA PATOLÓGICA E MEDICINA LEGAL | |
| local.publisher.initials | UFMG | |
| local.url.externa | https://www.tandfonline.com/doi/full/10.1080/00207454.2020.1744593 |
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