Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing

Paul Komminoth, Eva Kunz, Olaf Hiort, Sören Schröder, Xavier Matias-Guiu, Gudrun Christiansen, Jürgen Roth, Philipp U. Heitz

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59 Citations (Scopus)

Abstract

The suitability of formalin-fixed and paraffin-embedded tumor material was evaluated for molecular analysis of the RET proto-oncogene. We analyzed exons 10, 11, and 16 for point mutations in seven sporadic and six multiple endocrine neoplasia (MEN) 2A-associated pheochromocytomas by a nonradioactive single-strand conformation polymorphism assay followed by nonradioactive direct sequencing of PCR-amplified DNA using an automated DNA sequencer. All MEN 2A-associated pheochromocytomas contained a heterozygous missense germline mutation within cysteine codons of the cysteine-rich extracellular domain encoded by exons 10 and 11. Mutations were located in codon 619 (TGC→TCC; Cys→Ser) in one, in codon 635 (TGC→CGC; Cys→Arg) in three, and in codon 635 (TGC→TAC; Cys→Tyr) in two pheochromocytomas. No tumor-specific (somatic) mutations were detected in exons 10, 11, and 16 of the sporadic pheochromocytomas. These data support recent findings that germline point mutations that are clustered in distinct cysteine codons of the RET proto- oncogene are involved in the neoplastic phenotype of the MEN 2A syndrome. Our results demonstrate that both nonradioactive single-strand conformation polymorphism and direct sequencing are suitable methods to detect single base substitutions in DNA extracted from archival material.
Original languageEnglish
Pages (from-to)922-929
JournalAmerican Journal of Pathology
Volume145
Issue number4
Publication statusPublished - 1 Oct 1994

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