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Preparation of Formalin-fixed Paraffin-embedded Tissue Cores for both RNA and DNA Extraction.
Patel, Palak G; Selvarajah, Shamini; Boursalie, Suzanne; How, Nathan E; Ejdelman, Joshua; Guerard, Karl-Philippe; Bartlett, John M; Lapointe, Jacques; Park, Paul C; Okello, John B A; Berman, David M.
Afiliación
  • Patel PG; Department of Pathology & Molecular Medicine, Queen's University; Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University.
  • Selvarajah S; Department of Pathology & Molecular Medicine, Queen's University; Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University.
  • Boursalie S; Department of Pathology & Molecular Medicine, Queen's University; Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University.
  • How NE; Department of Pathology & Molecular Medicine, Queen's University; Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University.
  • Ejdelman J; Department of Surgery, Division of Urology, McGill University.
  • Guerard KP; Department of Surgery, Division of Urology, McGill University.
  • Bartlett JM; Transformative Pathology Program, Ontario Institute for Cancer Research (OICR).
  • Lapointe J; Department of Surgery, Division of Urology, McGill University.
  • Park PC; Department of Pathology & Molecular Medicine, Queen's University.
  • Okello JB; Department of Pathology & Molecular Medicine, Queen's University; Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University.
  • Berman DM; Department of Pathology & Molecular Medicine, Queen's University; Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University; bermand@queensu.ca.
J Vis Exp ; (114)2016 08 21.
Article en En | MEDLINE | ID: mdl-27583817
ABSTRACT
Formalin-fixed paraffin embedded tissue (FFPET) represents a valuable, well-annotated substrate for molecular investigations. The utility of FFPET in molecular analysis is complicated both by heterogeneous tissue composition and low yields when extracting nucleic acids. A literature search revealed a paucity of protocols addressing these issues, and none that showed a validated method for simultaneous extraction of RNA and DNA from regions of interest in FFPET. This method addresses both issues. Tissue specificity was achieved by mapping cancer areas of interest on microscope slides and transferring annotations onto FFPET blocks. Tissue cores were harvested from areas of interest using 0.6 mm microarray punches. Nucleic acid extraction was performed using a commercial FFPET extraction system, with modifications to homogenization, deparaffinization, and Proteinase K digestion steps to improve tissue digestion and increase nucleic acid yields. The modified protocol yields sufficient quantity and quality of nucleic acids for use in a number of downstream analyses, including a multi-analyte gene expression platform, as well as reverse transcriptase coupled real time PCR analysis of mRNA expression, and methylation-specific PCR (MSP) analysis of DNA methylation.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN / ARN / Fijación del Tejido / Adhesión en Parafina Límite: Humans Idioma: En Revista: J Vis Exp Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN / ARN / Fijación del Tejido / Adhesión en Parafina Límite: Humans Idioma: En Revista: J Vis Exp Año: 2016 Tipo del documento: Article