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Updated: Oct 2, 2025

Enhancing Tumor Content through Tumor Macrodissection
Published on: February 12, 2022
Enhancing Tumor Content through Tumor Macrodissection
Lee Wisner1, Brandon Larsen2, Alanna Maguire3
1Department of Research, Mayo Clinic.
Abstract:
The presence of contaminating non-tumor tissues in formalin-fixed paraffin-embedded (FFPE) tissues can greatly undermine genomic studies. Herein we describe macrodissection, a method designed to augment the percentage tumor content of a tissue specimen by removing and eliminating unwanted tissue prior to performing downstream nucleic acid extractions. FFPE tissue blocks were sectioned to produce 4-5 µm slide-mounted tissue sections. A representative section was submitted for hematoxylin and eosin (H&E) staining and subsequently reviewed by a board-certified pathologist. During the review, the pathologist identified and marked the regions of tumor tissue in the H&E. Once complete, the demarked H&E was used to guide resection of the serial unstained sections from the same tissue block. To demonstrate the effects of macrodissection, RNA extracted from matched macrodissected and non-dissected Diffuse Large B-Cell Lymphomas (DLBCL) were run on a digital gene expression assay capable of determining DLBCL subtype and BCL2 translocation status. The results showed that macrodissection changed the subtype or BCL2 translocation status calls in 60% of the samples examined. In conclusion, macrodissection is a simple and effective method for performing tumor enrichment prior to nucleic acid extractions, the product of which can then be confidently used in downstream genomic studies.
Insights
Macrodissection enriches tumor content in formalin-fixed paraffin-embedded tissues, improving genomic study accuracy. This method removes non-tumor tissues, significantly impacting Diffuse Large B-Cell Lymphoma subtype and BCL2 translocation status determination.
Area of Science:
- Pathology
- Genomics
- Molecular Biology
Background:
- Contaminating non-tumor tissues in FFPE samples compromise genomic study integrity.
- Accurate genomic analysis requires high tumor cell purity.
Purpose of the Study:
- To introduce and validate macrodissection as a method for increasing tumor content in FFPE tissues.
- To assess the impact of macrodissection on downstream genomic analyses, specifically for Diffuse Large B-Cell Lymphoma (DLBCL).
Main Methods:
- FFPE tissue blocks were sectioned, and a representative section was H&E stained.
- A pathologist identified and marked tumor regions on the H&E stained section.
- Macrodissection guided the removal of non-tumor tissue from serial unstained sections.
Main Results:
- RNA was extracted from macrodissected and non-dissected DLBCL samples.
- Digital gene expression assay determined DLBCL subtype and BCL2 translocation status.
- Macrodissection altered subtype or BCL2 translocation status calls in 60% of examined samples.
Conclusions:
- Macrodissection is a simple and effective technique for tumor enrichment in FFPE tissues.
- This method enhances the reliability of nucleic acid extracts for genomic studies.
- Macrodissection improves confidence in downstream genomic analysis results.

