Absence of mutations at codon 768 of the RET proto-oncogene in sporadic and hereditary pheochromocytomas.

Abstract:

:Sixteen sporadic pheochromocytomas, 3 pheochromocytomas in neurofibromatosis 1, and 4 pheochromocytomas in multiple endocrine neoplasia (MEN) 2A or 2B were screened for mutations at codon 768 of the RET proto-oncogene by AluI digestion of polymerase chain reaction PCR products and mutations in exon 13 by PCR-single strand conformation polymorphism (SSCP) analysis. Although mutations at codon 768 (GAG --> GAC; Glu --> Asp) of the RET proto-oncogene were recently reported to be found in 40% of sporadic medullary thyroid carcinomas (MTCs), the absence of missense mutations at codon 768 was confirmed both with PCR-restriction fragment length polymorphism (RFLP) and PCR-SSCP analysis in all examined cases of pheochromocytomas. These results suggest that mutations at codon 768 of the RET proto-oncogene do not represent a frequent mechanism of tumorigenesis for both sporadic and hereditary pheochromocytomas.

journal_name

Endocr J

journal_title

Endocrine journal

authors

Yoshimoto K,Kimura T,Tanaka C,Moritani M,Iwahana H,Itakura M

doi

10.1507/endocrj.43.109

subject

Has Abstract

pub_date

1996-02-01 00:00:00

pages

109-14

issue

1

eissn

0918-8959

issn

1348-4540

journal_volume

43

pub_type

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