HIF-1 α is associated with resistance to hypoxia-induced apoptosis in ameloblastoma
| dc.creator | Katherine Julissa Palma Valladares | |
| dc.creator | Sérgio de Melo Alves Júnior | |
| dc.creator | João de Jesus Viana Pinheiro | |
| dc.creator | Karolyny Martins Balbinot | |
| dc.creator | Antonia Taiane Lopes de Moraes | |
| dc.creator | Maria Sueli da Silva Kataoka | |
| dc.creator | Aline Maria Pereira Cruz Ramos | |
| dc.creator | Rommel Thiago Jucá Ramos | |
| dc.creator | Artur Luiz da Costa da Silva | |
| dc.creator | Ricardo Alves de Mesquita | |
| dc.creator | David Normando | |
| dc.date.accessioned | 2024-11-01T12:03:55Z | |
| dc.date.accessioned | 2025-09-09T00:55:08Z | |
| dc.date.available | 2024-11-01T12:03:55Z | |
| dc.date.issued | 2021 | |
| dc.description.sponsorship | CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico | |
| dc.format.mimetype | ||
| dc.identifier.doi | https://doi.org/10.1155/2021/3060375 | |
| dc.identifier.issn | 1687-8736 | |
| dc.identifier.uri | https://hdl.handle.net/1843/77769 | |
| dc.language | eng | |
| dc.publisher | Universidade Federal de Minas Gerais | |
| dc.relation.ispartof | International Journal of Dentistry | |
| dc.rights | Acesso Aberto | |
| dc.subject | Correlation of data | |
| dc.subject | Association | |
| dc.subject | Signal transduction | |
| dc.subject | Hypoxia | |
| dc.subject | Proteins | |
| dc.subject | Apoptosis regulatory proteins | |
| dc.title | HIF-1 α is associated with resistance to hypoxia-induced apoptosis in ameloblastoma | |
| dc.type | Artigo de periódico | |
| local.citation.epage | 10 | |
| local.citation.issue | 27 | |
| local.citation.spage | 1 | |
| local.citation.volume | 2021 | |
| local.description.resumo | Background: Ameloblastoma (AMB) is a benign odontogenic tumour, with an aggressive local behaviour and a high rate of recurrence. Previous studies have demonstrated that hypoxia-induced factor alpha 1 (HIF-1α) and activated caspase-3 contribute to tumour invasiveness and cytogenesis in ameloblastoma. Hypoxia increases HIF-1α levels, which triggers a number of signalling pathways. This paper aimed to present data in the study of hypoxia-activated signalling pathways that modulate proapoptotic and antiapoptotic events in AMB. Methods: Twenty cases of AMB and ten cases of dental follicle (DF) were used to analyse the immunoexpression of HIF-1α, p53, BNIP3, Bcl-2, IAP-2, GLUT1, and Bax. To contribute to the study, an analysis of expression and genetic interaction was performed using the cell line AME-1. Results: AMB and DF expressed the studied proteins. These proteins showed significantly greater immunoexpression in AMB compared with the DF (p < 0.05). HIF-1α showed an important association with GLUT1, and a positive correlation was observed among p53, Bcl-2, and IAP-2. Transcriptomic analysis showed the significant expression of the studied proteins, and the network generated showed a direct association of HIF-1αF with GLUT1 (SLC2A1), TP53, and LDHA. Interestingly, GLUT1 also exhibited direct interaction with TP53 and LDHA. Conclusion: In AMB tumorigenesis, hypoxia is possibly related to antiapoptotic events, which suggests an important role for HIF-1α, GLUT1, Bcl-2, IAP-2, and possibly p53. | |
| local.identifier.orcid | https://orcid.org/0000-0003-4721-8165 | |
| local.identifier.orcid | https://orcid.org/0000-0003-0272-9279 | |
| local.identifier.orcid | https://orcid.org/0000-0002-6914-6441 | |
| local.identifier.orcid | https://orcid.org/0000-0003-2507-0243 | |
| local.identifier.orcid | https://orcid.org/0000-0003-2719-3634 | |
| local.identifier.orcid | https://orcid.org/0000-0001-9650-1034 | |
| local.identifier.orcid | https://orcid.org/0000-0003-3207-4007 | |
| local.identifier.orcid | https://orcid.org/0000-0002-1335-1040 | |
| local.identifier.orcid | https://orcid.org/0000-0001-8812-2923 | |
| local.identifier.orcid | https://orcid.org/0000-0002-8032-1474 | |
| local.identifier.orcid | https://orcid.org/0000-0002-4082-1132 | |
| local.publisher.country | Brasil | |
| local.publisher.department | FAO - DEPARTAMENTO DE CLÍNICA | |
| local.publisher.initials | UFMG | |
| local.url.externa | https://onlinelibrary.wiley.com/doi/10.1155/2021/3060375 |