دورية أكاديمية
TNFRSF1B Gene Variants in Clinicopathological Aspects and Prognosis of Patients with Cutaneous Melanoma
| العنوان: | TNFRSF1B Gene Variants in Clinicopathological Aspects and Prognosis of Patients with Cutaneous Melanoma |
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| المؤلفون: | Bruna Fernandes Carvalho, Gabriela Vilas Bôas Gomez, Juliana Carron, Ligia Traldi Macedo, Gisele Melo Gonçalves, Vinicius de Lima Vazquez, Sergio Vicente Serrano, Gustavo Jacob Lourenço, Carmen Silvia Passos Lima |
| المصدر: | International Journal of Molecular Sciences, Vol 25, Iss 5, p 2868 (2024) |
| بيانات النشر: | MDPI AG, 2024. |
| سنة النشر: | 2024 |
| المجموعة: | LCC:Biology (General) LCC:Chemistry |
| مصطلحات موضوعية: | cutaneous melanoma, TNFRSF1B, single nucleotide variant, clinicopathological aspects, survival, Biology (General), QH301-705.5, Chemistry, QD1-999 |
| الوصف: | Regulatory T lymphocytes play a critical role in immune regulation and are involved in the aberrant cell elimination by facilitating tumor necrosis factor connection to the TNFR2 receptor, encoded by the TNFRSF1B polymorphic gene. We aimed to examine the effects of single nucleotide variants TNFRSF1B c.587T>G, c.*188A>G, c.*215C>T, and c.*922C>T on the clinicopathological characteristics and survival of cutaneous melanoma (CM) patients. Patients were genotyped using RT-PCR. TNFRSF1B levels were measured using qPCR. Luciferase reporter assay evaluated the interaction of miR-96 and miR-1271 with the 3′-UTR of TNFRSF1B. The c.587TT genotype was more common in patients younger than 54 years old than in older patients. Patients with c.*922CT or TT, c.587TG or GG + c.*922CT or TT genotypes, as well as those with the haplotype TATT, presented a higher risk of tumor progression and death due to the disease effects. Individuals with the c.*922TT genotype had a higher TNFRSF1B expression than those with the CC genotype. miR-1271 had less efficient binding with the 3′-UTR of the T allele when compared with the C allele of the SNV c.*922C>T. Our findings, for the first time, demonstrate that TNFRSF1B c.587T>G and c.*922C>T variants can serve as independent prognostic factors in CM patients. |
| نوع الوثيقة: | article |
| وصف الملف: | electronic resource |
| اللغة: | English |
| تدمد: | 1422-0067 1661-6596 64236994 |
| Relation: | https://www.mdpi.com/1422-0067/25/5/2868; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067 |
| DOI: | 10.3390/ijms25052868 |
| URL الوصول: | https://doaj.org/article/e36b04720cf642369945d3a7636c6eb8 |
| رقم الأكسشن: | edsdoj.36b04720cf642369945d3a7636c6eb8 |
| قاعدة البيانات: | Directory of Open Access Journals |
Full Text Finder | تدمد: | 14220067 16616596 64236994 |
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| DOI: | 10.3390/ijms25052868 |