A nondestructive molecule extraction method allowing morphological and molecular analyses using a single tissue section

In clinical practice, molecular analysis of tumor specimens is often restricted by available technology for sample preparation. Virtually all current methods require homogenization of tissues for molecule extraction. We have developed a simple, rapid, nondestructive molecule extraction (NDME) method...

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Bibliographic Details
Published in:Laboratory investigation Vol. 85; no. 11; pp. 1416 - 1428
Main Authors: CHU, Wei-Sing, QI LIANG, JILAN LIU, MIN QI WEI, WINTERS, Mary, LIOTTA, Lance, SANDBERG, Glenn, MAOKAI GONG
Format: Journal Article
Language:English
Published: New York, NY Nature Publishing 01-11-2005
Nature Publishing Group
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Summary:In clinical practice, molecular analysis of tumor specimens is often restricted by available technology for sample preparation. Virtually all current methods require homogenization of tissues for molecule extraction. We have developed a simple, rapid, nondestructive molecule extraction (NDME) method to extract proteins and nucleic acids directly from a single fixed or frozen tissue section without destroying the tissue morphology. The NDME method is based upon exposure of micron-thick tissue section to extraction buffer with the help of heating and/or intact physical forces (ultrasound and microwave) to facilitate release of macromolecules into the buffer. The extracted proteins and nucleic acids can be used directly without further purification for downstream SDS-PAGE analysis, immunoblotting, protein array, mass spectra protein profiling, PCR, and RT-PCR reactions. Most importantly, the NDME procedure also serves as an antigen retrieval treatment, so that after NDME, the same tissue section can be used for histopathological analyses, such as H&E staining, immunohistochemistry, and in situ hybridization. Thus, the NDME method allows, for the first time, both histological diagnosis and molecular analysis on a single tissue section, whether it is from frozen or fixed tissue specimens.
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ISSN:0023-6837
1530-0307
DOI:10.1038/labinvest.3700337