Literature DB >> 11227733

RET proto-oncogene mutation in a mixed medullary-follicular thyroid carcinoma.

F Orlandi1, E Chiefari, P Caraci, A Mussa, I Gonzatto, P De Giuli, D Giuffrida, A Angeli, S Filetti.   

Abstract

A case of a patient with an uncommon thyroid carcinoma, showing histological and immunohistochemical features of both follicular and parafollicular cells is described. Somatic point mutation (ATG to ACG heterozygotic mutation at codon 918) of the RET proto-oncogene was detected in tumor tissue, as confirmed by immunohistochemical expression of RET oncoprotein. Our findings suggest that constitutive RET proto-oncogene activation may be involved in the development of mixed medullary-follicular thyroid carcinoma.

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Year:  2001        PMID: 11227733     DOI: 10.1007/BF03343809

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  19 in total

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Journal:  Am J Surg Pathol       Date:  1996-02       Impact factor: 6.394

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Journal:  Thyroid       Date:  1991       Impact factor: 6.568

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  2 in total

1.  The oncogenic activity of RET point mutants for follicular thyroid cells may account for the occurrence of papillary thyroid carcinoma in patients affected by familial medullary thyroid carcinoma.

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Journal:  Am J Pathol       Date:  2004-08       Impact factor: 4.307

Review 2.  Goblet cell carcinoids and other mixed neuroendocrine/nonneuroendocrine neoplasms.

Authors:  Marco Volante; Luisella Righi; Sofia Asioli; Gianni Bussolati; Mauro Papotti
Journal:  Virchows Arch       Date:  2007-08-08       Impact factor: 4.064

  2 in total

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