Literature DB >> 10363573

Somatic mutation of the APC gene in thyroid carcinoma associated with familial adenomatous polyposis.

T Iwama1, M Konishi, T Iijima, K Yoshinaga, T Tominaga, M Koike, M Miyaki.   

Abstract

We report the existence of both germline and somatic mutations of the APC gene in thyroid carcinomas from familial adenomatous polyposis (FAP) patients. One papillary thyroid carcinoma from a 210-year-old woman, with germline mutation of the APC gene (TCA to TGA at codon 1110), showed a somatic mutation of AAAAC deletion between codons 1060 and 1063. Another somatic mutation of CAG to TAG at codon 886 was also found in one of multiple thyroid carcinomas from a 26-year-old woman with attenuated FAP and germline mutation at codon 175 (C deletion). This is the first evidence that total absence of the normal function of the APC gene is involved in development of thyroid carcinomas in FAP.

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Year:  1999        PMID: 10363573      PMCID: PMC5926080          DOI: 10.1111/j.1349-7006.1999.tb00757.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


  29 in total

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Authors:  W A McAdam; J C Goligher
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4.  Loss of normal allele of the APC gene in an adrenocortical carcinoma from a patient with familial adenomatous polyposis.

Authors:  M Seki; K Tanaka; R Kikuchi-Yanoshita; M Konishi; H Fukunari; T Iwama; M Miyaki
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7.  Coexistence of somatic and germ-line mutations of APC gene in desmoid tumors from patients with familial adenomatous polyposis.

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6.  Nuclear localization of immunoreactive beta-catenin is specific to familial adenomatous polyposis in papillary thyroid carcinoma.

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7.  A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis.

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Review 9.  Influencers on Thyroid Cancer Onset: Molecular Genetic Basis.

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Review 10.  Genetic Mutations and Variants in the Susceptibility of Familial Non-Medullary Thyroid Cancer.

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  10 in total

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