Absence of mutations in the MEN2A region of the ret proto-oncogene in non-MEN 2A phaeochromocytomas

Clin Endocrinol (Oxf). 1995 Jan;42(1):17-21. doi: 10.1111/j.1365-2265.1995.tb02593.x.

Abstract

Objective: To determine the presence of abnormalities of the MEN2A region of the ret proto-oncogene in phaeochromocytomas/paragangliomas (PHAEO) of different aetiologies.

Design: Total RNA was extracted from tumours and used as templates for reverse transcriptase polymerase chain reactions. A ret primer pair, which encompasses the region which is mutated in the germ-line of patients with MEN 2A, was used. The resulting 262-bp product was sequenced.

Patients: Ten PHAEOs were examined. Four tumours were from von Hippel-Lindau disease patients; five were sporadic, isolated tumours; one from a patient with multiple endocrine neoplasia type 2A (MEN 2A). The medullary thyroid cancer from the single MEN 2A patient was also examined.

Results: A heterozygous TGC to CGC mutation of codon 634 (cysteine to arginine) was found in the PHAEO and medullary thyroid cancer from the MEN 2A patient. The 262-bp ret fragment was not found in two tumours (one malignant PHAEO and one secretory paraganglioma), although the intra-cellular ret tyrosine kinase domain was detected in these tumours. The cysteine codons were normal in all other non-MEN 2A PHAEOs.

Conclusion: Mutations of key cysteine codons of the ret proto-oncogene may be specific to MEN 2A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Gland Neoplasms / genetics*
  • Arginine
  • Base Sequence
  • Codon
  • Cysteine
  • Drosophila Proteins*
  • Humans
  • Molecular Sequence Data
  • Multiple Endocrine Neoplasia Type 2a / genetics*
  • Paraganglioma / genetics
  • Pheochromocytoma / genetics*
  • Point Mutation / genetics*
  • Polymerase Chain Reaction
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-ret
  • Proto-Oncogenes / genetics*
  • Receptor Protein-Tyrosine Kinases / genetics

Substances

  • Codon
  • Drosophila Proteins
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Arginine
  • Proto-Oncogene Proteins c-ret
  • Receptor Protein-Tyrosine Kinases
  • Ret protein, Drosophila
  • Cysteine