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Accuracy and Clinical Relevance of Intra-Tumoral Fusobacterium nucleatum Detection in Formalin-Fixed Paraffin-Embedded (FFPE) Tissue by Droplet Digital PCR (ddPCR) in Colorectal Cancer.
Datorre, José Guilherme; de Carvalho, Ana Carolina; Dos Reis, Mariana Bisarro; Dos Reis, Monise; Matsushita, Marcus; Santos, Florinda; Guimarães, Denise Peixoto; Reis, Rui Manuel.
Afiliación
  • Datorre JG; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • de Carvalho AC; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • Dos Reis MB; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • Dos Reis M; Department of Pathology, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • Matsushita M; Department of Pathology, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • Santos F; Department of Medical Oncology, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • Guimarães DP; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos 14784400, Brazil.
  • Reis RM; Department of Prevention, Barretos Cancer Hospital, Barretos 14784400, Brazil.
Diagnostics (Basel) ; 12(1)2022 Jan 05.
Article en En | MEDLINE | ID: mdl-35054281
ABSTRACT
The use of droplet digital PCR (ddPCR) to identify and quantify low-abundance targets is a significant advantage for accurately detecting potentially oncogenic bacteria. Fusobacterium nucleatum (Fn) is implicated in colorectal cancer (CRC) tumorigenesis and is becoming an important prognostic biomarker. We evaluated the detection accuracy and clinical relevance of Fn DNA by ddPCR in a molecularly characterized, formalin-fixed, paraffin-embedded (FFPE) CRC cohort previously analyzed by qPCR for Fn levels. Following a ddPCR assay optimization and an analytical evaluation, Fn DNA were measured in 139 CRC FFPE cases. The measures of accuracy for Fn status compared to the prior results generated by qPCR and the association with clinicopathological and molecular patients' features were also evaluated. The ddPCR-based Fn assay was sensitive and specific to positive controls. Fn DNA were detected in 20.1% of cases and further classified as Fn-high and Fn-low/negative, according to the median amount of Fn DNA that were detected in all cases and associated with the patient's worst prognosis. There was a low agreement between the Fn status determined by ddPCR and qPCR (Cohen's Kappa = 0.210). Our findings show that ddPCR can detect and quantify Fn in FFPE tumor tissues and highlights its clinical relevance in Fn detection in a routine CRC setting.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Diagnostics (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Diagnostics (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Brasil