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A Novel DNA Variant in SMARCA4 Gene Found in a Patient Affected by Early Onset Colon Cancer.
Di Maggio, Federica; Boccia, Giuseppe; Nunziato, Marcella; Filotico, Marcello; Montesarchio, Vincenzo; D'Armiento, Maria; Corcione, Francesco; Salvatore, Francesco.
Afiliação
  • Di Maggio F; CEINGE-Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy.
  • Boccia G; Department of Molecular Medicine and Medical Biotechnologies, University of Naples "Federico II", 80131 Naples, Italy.
  • Nunziato M; Department of Public Health, University of Naples "Federico II", 80131 Naples, Italy.
  • Filotico M; CEINGE-Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy.
  • Montesarchio V; Department of Molecular Medicine and Medical Biotechnologies, University of Naples "Federico II", 80131 Naples, Italy.
  • D'Armiento M; Department of Public Health, University of Naples "Federico II", 80131 Naples, Italy.
  • Corcione F; Division of Medical Oncology, AORN dei Colli-Monaldi Hospital, 80131 Naples, Italy.
  • Salvatore F; Pathology Unit, Department of Public Health, University of Naples "Federico II", 80131 Naples, Italy.
Int J Mol Sci ; 25(5)2024 Feb 27.
Article em En | MEDLINE | ID: mdl-38473962
ABSTRACT
Colorectal cancer is the third leading cause of death from neoplasia worldwide. Thanks to new screening programs, we are now seeing an increase in Early Onset of ColoRectal Cancer (EOCRC) in patients below the age of 50. Herein, we report a clinical case of a woman affected by EOCRC. This case illustrates the importance of genetic predisposition testing also in tumor patients. Indeed, for our patient, we used a combined approach of multiple molecular and cellular biology technologies that revealed the presence of an interesting novel variant in the SMARCA4 gene. The latter gene is implicated in damage repair processes and related, if mutated, to the onset of various tumor types. In addition, we stabilized Patient-Derived Organoids from the tumor tissue of the same patient and the result confirmed the presence of this novel pathogenic variant that has never been found before even in early onset cancer. In conclusion, with this clinical case, we want to underscore the importance of including patients even those below the age of 50 years in appropriate screening programs which should also include genetic tests for predisposition to early onset cancers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias do Colo Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias do Colo Idioma: En Ano de publicação: 2024 Tipo de documento: Article