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Use of TP53 reference materials to validate mutations in clinical tissue specimens by single-strand conformational polymorphism analysis

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Abstract

Background: As genetic information moves from basic research laboratories in to the clinical testing environment, there is a critical need for reliable reference materials for the quality assurance of genetic tests. A panel of 12 plasmid clones containing wild-type or point mutations within exons 5–9 have been developed as reference materials for the detection of TP53 mutations.

Aim: The goal of this study was to validate the reference materials in providing quality assurance for the detection of TP53 mutations in clinical specimens.

Methods: We studied 33 gynecological samples, 11 apparently normal samples and 22 malignant tumors of various origins. Mutations were identified using single-strand conformational polymorphism analysis with both slab gel and capillary electrophoresis. All DNA samples were amplified with fluorescently labeled PCR primers specific for exons 5–9 for mutation detection.

Results: Of the 33 patient samples tested, mutations and polymorphisms were found in six specimens in three of the five exons scanned; no mutations were found in exons 7 or 9. Both a mutation and polymorphism were found in non-malignant specimens from the control group. The mutations were confirmed by DNA sequence analysis of the regions scanned.

Conclusions: Mutations and polymorphisms were detected in the clinical samples. All of the mutations were silent except for one non-conservative mutation in exon 5, codon 181. This study demonstrates the usefulness of the National Institute of Standards and Technology (NIST) TP53 reference panel in TP53 mutation detection in clinical tissue specimens.

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Acknowledgements

Certain commercial equipment, instruments, materials, or companies are identified in this paper to specify adequately the experimental procedure. Such identification does not imply recommendation nor endorsement by the National Institute of Standards and Technology, nor does it imply that the materials or equipment identified are the best available for the purpose.

Dr Sunar-Reeder and Dr Atha contributed equally to the study.

This study was funded using funds appropriated by the Congress of the United States to the National Institute of Standards and Technology, an agency of the United States government. The authors were federal employees at the time the article was written and are subject to the conflict of interest laws governing federal employees.

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Correspondence to Catherine D. O’Connell.

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Sunar-Reeder, B., Atha, D.H., Aydemir, S. et al. Use of TP53 reference materials to validate mutations in clinical tissue specimens by single-strand conformational polymorphism analysis. CNS Drugs 8, 123–130 (2004). https://doi.org/10.1007/BF03260055

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