BRAFV600E mutation in the pathogenesis of a large series of papillary thyroid carcinoma in Czech Republic
Jazyk angličtina Země Itálie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20009493
DOI
10.1007/bf03346593
PII: 6722
Knihovny.cz E-zdroje
- MeSH
- černobylská havárie MeSH
- DNA nádorová biosyntéza genetika MeSH
- dospělí MeSH
- exony genetika MeSH
- frekvence genu MeSH
- invazivní růst nádoru genetika MeSH
- kodon genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace fyziologie MeSH
- nádory štítné žlázy epidemiologie genetika patologie MeSH
- papilární karcinom epidemiologie genetika patologie MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- polymorfismus konformace jednovláknové DNA genetika MeSH
- protoonkogenní proteiny B-Raf genetika MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- věkové faktory MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika epidemiologie MeSH
- Názvy látek
- BRAF protein, human MeSH Prohlížeč
- DNA nádorová MeSH
- kodon MeSH
- protoonkogenní proteiny B-Raf MeSH
BACKGROUND: Activating point mutation of the BRAF gene, the most common genetic alteration reported in papillary thyroid carcinomas (PTC), has been associated with poor prognostic characteristics. AIM: Our objective was to determine the frequency of BRAFV600E mutation in PTC tumor tissues from the period 1960-2007 and to correlate it with clinicopathological parameters. SUBJECTS AND METHODS: DNAs were extracted from 242 PTCs, 23 sporadic medullary carcinomas, one anaplastic carcinoma and 6 poorly differentiated carcinomas. The presence of BRAFV600E mutation was determined using single strand conformation polymorphism method and verified by direct sequencing. RESULTS: BRAFV600E mutation was detected in 81 of 242 PTCs (33.5%), in one of 6 poorly differentiated carcinomas (16.7%) and in anaplastic carcinoma. BRAFV600E mutation was much less frequent in the follicular variant compared to classical variant and mixed follicular- classical variant of PTCs (p=0.001). BRAFV600E mutation was significantly associated with presence of nodal metastasis (p=0.029), more advanced TNM stage (p=0.014) and recurrence of disease (p=0.008). The mutation correlated with a higher age at diagnosis (p=0.049) and with a greater tumor size (p=0.041). Multivariate analysis confirmed these findings. The prevalence of BRAFV600E mutation before 1986 was significantly lower than after it (p=0.008). CONCLUSIONS: Our data suggest that BRAFV600E mutation is associated with high-risk clinicopathological characteristics of PTC and worse prognosis of patients. The frequency of the mutation significantly varied during the observed period but rather because of the different age distribution of patients in particular periods than as a consequence of Chernobyl accident.
Zobrazit více v PubMed
Nature. 1995 Jun 1;375(6530):365 PubMed
CA Cancer J Clin. 2005 Jul-Aug;55(4):242-58; quiz 261-2, 264 PubMed
Cancer Res. 1997 May 1;57(9):1690-4 PubMed
J Clin Endocrinol Metab. 2004 Oct;89(10):5175-80 PubMed
Oncogene. 2003 Sep 25;22(41):6455-7 PubMed
Biol Cell. 2001 Sep;93(1-2):53-62 PubMed
Cell. 2004 Mar 19;116(6):855-67 PubMed
Int J Cancer. 1999 Mar 15;80(6):842-7 PubMed
Nature. 1992 Sep 3;359(6390):21 PubMed
J Clin Invest. 2005 Jan;115(1):94-101 PubMed
Endocr J. 2009;56(1):89-97 PubMed
Anticancer Res. 2008 Jan-Feb;28(1A):305-8 PubMed
J Natl Cancer Inst. 2003 Apr 16;95(8):625-7 PubMed
Clin Endocrinol (Oxf). 2004 Aug;61(2):239-43 PubMed
J Clin Endocrinol Metab. 2003 Nov;88(11):5399-404 PubMed
Endocr Relat Cancer. 2006 Mar;13(1):257-69 PubMed
Cancer Lett. 2004 Jun 8;209(1):1-6 PubMed
J Clin Endocrinol Metab. 1999 Nov;84(11):4232-8 PubMed
Br J Cancer. 2000 Jan;82(2):315-22 PubMed
J Clin Endocrinol Metab. 2006 Sep;91(9):3667-70 PubMed
Endocr Rev. 2007 Dec;28(7):742-62 PubMed
Nat Genet. 2003 Jan;33(1):19-20 PubMed
J Clin Endocrinol Metab. 2004 Sep;89(9):4267-71 PubMed
Cancer. 1999 Jul 1;86(1):149-56 PubMed
Ann Surg. 2006 Nov;244(5):799-804 PubMed
Oncogene. 2003 Oct 9;22(44):6942-5 PubMed
Yonsei Med J. 2004 Oct 31;45(5):818-21 PubMed
Cancer Res. 2003 Apr 1;63(7):1454-7 PubMed
Eur J Cancer. 2005 Mar;41(5):816-21 PubMed
Cancer Res. 2003 Aug 1;63(15):4561-7 PubMed
Oncogene. 2003 Jul 17;22(29):4578-80 PubMed
Cancer. 2009 Mar 1;115(5):972-80 PubMed
Lab Invest. 2005 Sep;85(9):1065-75 PubMed
Nature. 2002 Jun 27;417(6892):949-54 PubMed
Virchows Arch. 2005 Jun;446(6):589-95 PubMed
J Clin Endocrinol Metab. 2005 Dec;90(12):6373-9 PubMed
J Clin Endocrinol Metab. 2004 Mar;89(3):1365-8 PubMed
Clin Endocrinol (Oxf). 2005 Oct;63(4):461-6 PubMed
J Proteome Res. 2007 Feb;6(2):469-79 PubMed
J Pathol. 1998 May;185(1):71-8 PubMed
Med Sci Monit. 2004 Jul;10(7):CR300-6 PubMed
J Clin Endocrinol Metab. 2003 Sep;88(9):4393-7 PubMed
Ann Surg. 2007 Sep;246(3):466-70; discussion 470-1 PubMed
J Clin Endocrinol Metab. 2007 Nov;92(11):4085-90 PubMed
Cancer. 2006 Feb 1;106(3):524-31 PubMed
Oncogene. 1996 Aug 15;13(4):687-93 PubMed
J Pathol. 2004 Feb;202(2):247-51 PubMed
Differential Clinicopathological Risk and Prognosis of Major Papillary Thyroid Cancer Variants
A 3-bp Deletion VK600-1E in the BRAF Gene Detected in a Young Woman with Papillary Thyroid Carcinoma
Association between BRAF V600E mutation and recurrence of papillary thyroid cancer