Your browser doesn't support javascript.
loading
Detection of Cancer-Associated Gene Mutations in Urinary Cell-Free DNA among Prostate Cancer Patients in South Africa.
Temilola, Dada Oluwaseyi; Wium, Martha; Paccez, Juliano; Salukazana, Azola Samkele; Rotimi, Solomon O; Otu, Hasan H; Carbone, Giuseppina M; Kaestner, Lisa; Cacciatore, Stefano; Zerbini, Luiz Fernando.
Afiliação
  • Temilola DO; International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town 7925, South Africa.
  • Wium M; Integrative Biomedical Sciences Division, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
  • Paccez J; International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town 7925, South Africa.
  • Salukazana AS; International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town 7925, South Africa.
  • Rotimi SO; Division of Urology, University of Cape Town, Groote Schuur Hospital, Cape Town 7925, South Africa.
  • Otu HH; Biochemistry Department, Covenant University, Ota 112104, Nigeria.
  • Carbone GM; Department of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588, USA.
  • Kaestner L; Institute of Oncology Research (IOR), Università della Svizzera italiana, 6900 Bellinzona, Switzerland.
  • Cacciatore S; Division of Urology, University of Cape Town, Groote Schuur Hospital, Cape Town 7925, South Africa.
  • Zerbini LF; International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town 7925, South Africa.
Genes (Basel) ; 14(10)2023 09 27.
Article em En | MEDLINE | ID: mdl-37895233
ABSTRACT
Prostate cancer (PCa) is the most common cause of cancer death among African men. The presence of tumor-specific variations in cell-free DNA (cfDNA), such as mutations, microsatellite instability, and DNA methylation, has been explored as a source of biomarkers for cancer diagnosis. In this study, we investigated the diagnostic role of cfDNA among South African PCa patients. We performed whole exome sequencing (WES) of urinary cfDNA. We identified a novel panel of 31 significantly deregulated somatic mutated genes between PCa and benign prostatic hyperplasia (BPH). Additionally, we performed whole-genome sequencing (WGS) on matching PCa and normal prostate tissue in an independent PCa cohort from South Africa. Our results suggest that the mutations are of germline origin as they were also found in the normal prostate tissue. In conclusion, our study contributes to the knowledge of cfDNA as a biomarker for diagnosing PCa in the South African population.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperplasia Prostática / Neoplasias da Próstata / Ácidos Nucleicos Livres Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperplasia Prostática / Neoplasias da Próstata / Ácidos Nucleicos Livres Idioma: En Ano de publicação: 2023 Tipo de documento: Article