| Texto completo | |
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Munari, Fernanda Franco
[1]
;
dos Santos, Wellington
[1]
;
Evangelista, Adriane Feijo
[1]
;
Carvalho, Ana Carolina
[1]
;
Pastrez, Paula Aguiar
[1]
;
Bugatti, Diego
[2]
;
Wohnrath, Durval R.
[2]
;
Scapulatempo-Neto, Cristovam
[3, 1]
;
Guimaraes, Denise Peixoto
[4, 1]
;
Longatto-Filho, Adhemar
[5, 6, 7, 1]
;
Reis, Rui Manuel
[5, 6, 1]
Número total de Autores: 11
|
| Afiliação do(s) autor(es): | [1] Barretos Canc Hosp, Mol Oncol Res Ctr, Antenor Duarte Villela 1331, BR-14784400 Barretos, SP - Brazil
[2] Barretos Canc Hosp, Dept Upper Digest, Barretos - Brazil
[3] Barretos Canc Hosp, Dept Pathol, Barretos - Brazil
[4] Barretos Canc Hosp, Dept Endoscopy, Barretos - Brazil
[5] ICVS 3Bs PT Govt Associate Lab, Braga, Guimaraes - Portugal
[6] Univ Minho, Sch Med, Life & Hlth Sci Res Inst ICVS, Braga - Portugal
[7] Univ Sao Paulo, Med Sch, Dept Pathol, Med Lab Med Invest LIM 14, Sao Paulo - Brazil
Número total de Afiliações: 7
|
| Tipo de documento: | Artigo Científico |
| Fonte: | SCIENTIFIC REPORTS; v. 11, n. 1 OCT 18 2021. |
| Citações Web of Science: | 0 |
| Resumo | |
Esophageal cancer is an aggressive tumor that has a high rate of incidence and mortality worldwide. It is the 10th most frequent type in Brazil, being squamous cell carcinoma (ESCC) the predominant subtype. There is currently an incessant search to identify the frequently altered genes associated with esophageal squamous cell carcinoma biology that could be druggable. This study aimed to analyze the somatic mutation profile of a large panel of cancer-related genes in Brazilian ESCC. In a series of 46 ESCC diagnoses at Barretos Cancer Hospital, DNA isolated from paired fresh-frozen and blood tissue, a panel of 150 cancer-related genes was analyzed by next-generation sequencing. The genes with the highest frequency of mutations were TP53 (39/46, 84.8%), followed by NOTCH1 ( 7/46, 15.2%), NFE2L2 ( 5/46, 10.8%), RB1 (3/46, 6.5%), PTEN (3/46, 6.5%), CDKN2A (3/46, 6.5%), PTCH1 (2/46, 4.3%) and PIK3CA (2/46, 4.3%). There was no significant association between molecular and patients' clinicopathological features. Applying an evolutionary action score of p53 ( EAp53), we observed that 14 (35.9%) TP53 mutations were classified as high-risk, yet no association with overall survival was observed. Concluding, this the largest mutation profile of Brazilian ESCC patients, which helps in the elucidation of the major cancer-related genes in this population. (AU) | |
| Processo FAPESP: | 15/20077-3 - Detecção de DNA de HPV de alto risco e análises do status mutacional dos genes KRAS e PIK3CA e do painel de citocinas inflamatórias em pacientes com câncer de esôfago e megaesôfago chagásico com e sem câncer |
| Beneficiário: | Fernanda Franco Munari |
| Modalidade de apoio: | Bolsas no Brasil - Mestrado |