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Ultra-Rapid Droplet Digital PCR Enables Intraoperative Tumor Quantification.
Murphy, Zachary R; Bianchini, Emilia C; Smith, Andrew; Körner, Lisa I; Russell, Teresa; Reinecke, David; Wang, Yuxiu; Snuderl, Matija; Orringer, Daniel A; Evrony, Gilad D.
Afiliación
  • Murphy ZR; Center for Human Genetics and Genomics, New York University Grossman School of Medicine, USA.
  • Bianchini EC; Department of Pediatrics, Department of Neuroscience & Physiology, Institute for Systems Genetics, Laura and Isaac Perlmutter Cancer Center, and Neuroscience Institute, New York University Grossman School of Medicine, USA.
  • Smith A; Center for Human Genetics and Genomics, New York University Grossman School of Medicine, USA.
  • Körner LI; Department of Pediatrics, Department of Neuroscience & Physiology, Institute for Systems Genetics, Laura and Isaac Perlmutter Cancer Center, and Neuroscience Institute, New York University Grossman School of Medicine, USA.
  • Russell T; Department of Neurosurgery, New York University Grossman School of Medicine, USA.
  • Reinecke D; Department of Neurosurgery, New York University Grossman School of Medicine, USA.
  • Wang Y; Department of Neurosurgery, New York University Grossman School of Medicine, USA.
  • Snuderl M; Department of Neurosurgery, New York University Grossman School of Medicine, USA.
  • Orringer DA; Department of Pathology, New York University Grossman School of Medicine, USA.
  • Evrony GD; Brain and Spine Tumor Center, Laura and Isaac Perlmutter Cancer Center, New York University Langone Health.
medRxiv ; 2024 May 31.
Article en En | MEDLINE | ID: mdl-38854127
ABSTRACT
The diagnosis and treatment of tumors often depends on molecular-genetic data. However, rapid and iterative access to molecular data is not currently feasible during surgery, complicating intraoperative diagnosis and precluding measurement of tumor cell burdens at surgical margins to guide resections. To address this gap, we developed Ultra-Rapid droplet digital PCR (UR-ddPCR), which can be completed in 15 minutes from tissue to result with an accuracy comparable to standard ddPCR. We demonstrate UR-ddPCR assays for the IDH1 R132H and BRAF V600E clonal mutations that are present in many low-grade gliomas and melanomas, respectively. We illustrate the clinical feasibility of UR-ddPCR by performing it intraoperatively for 13 glioma cases. We further combine UR-ddPCR measurements with UR-stimulated Raman histology intraoperatively to estimate tumor cell densities in addition to tumor cell percentages. We anticipate that UR-ddPCR, along with future refinements in assay instrumentation, will enable novel point-of-care diagnostics and the development of molecularly-guided surgeries that improve clinical outcomes.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: MedRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: MedRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos