BRAFV600E mutation, but not RET/PTC rearrangements, is correlated with a lower expression of both thyroperoxidase and sodium iodide symporter genes in papillary thyroid cancer

被引:123
作者
Romei, Cristina [2 ]
Ciampi, Raffaele [2 ]
Faviana, Pinuccia [3 ]
Agate, Laura [2 ]
Molinaro, Eleonora [2 ]
Bottici, Valeria [2 ]
Basolo, Fulvio [3 ]
Miccoli, Paolo [4 ]
Pacini, Furio [5 ]
Pinchera, Aldo [1 ,2 ]
Elisei, Rossella [1 ,2 ]
机构
[1] Univ Pisa, Dept Endocrinol, AMBISEN Ctr, Ctr High Technol,Study Environm Damage Endocrine, I-56124 Pisa, Italy
[2] Univ Pisa, Dept Endocrinol & Metab, I-56100 Pisa, Italy
[3] Univ Pisa, Dept Oncol, I-56100 Pisa, Italy
[4] Univ Pisa, Dept Surg, I-56100 Pisa, Italy
[5] Univ Siena, Dept Internal Med, I-53100 Siena, Italy
关键词
D O I
10.1677/ERC-07-0130
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A low sodium iodide symporter (NIS) expression has been shown in papillary thyroid carcinomas (PTCs) harboring the BRAF(V600E) mutation. In the present study, we analyzed the mRNA expression of thyroid differentiation genes, glucose transporter (GLUT)-1 and GLUT-3, in 78 PTCs according to the presence of BRAF(V600E) or RET/PTC rearrangements. We found BRAF(V600E) and RET/PTC rearrangements in 35.8 and 19.4% of PTCs respectively. The mRNA expression of NIS and thyroperoxidase (TPO) genes were significantly lower (P<0.0001 and P=0.004 respectively) in BRAF(V600E)-positive PTC with respect to non-mutated samples. In support of this result, immunohistochemistry showed that the percentage of NIS-positive cells was significantly lower (P=0.005) in BRAF(V600E)-mutated PTC (mean 53.5%) than in negative cases (mean 72.6%). In contrast, no difference either in NIS or in any other thyroid differentiation genes' mRNA expression was found in PTC with or without RET/PTC rearrangements. When GLUT-11 and GLUT-3 mRNA expression was considered, no correlation was found either in BRAF(V600E)-nor in RET/PTC-mutated cases. In conclusion, this study confirmed the presence of a genetic alteration of BRAF and/or RET oncogenes in 64% of PTC cases and revealed a significant correlation of BRAF(V600E) mutation with a lower expression of both NIS and TPO. This latter finding could indicate that an early dedifferentiation process is present at the molecular level in BRAF(V600E)-mutated PTC, thus suggesting that the previously demonstrated poor prognostic significance of BRAF(V600E) mutation could be related to the dedifferentiation process more than to a more advanced stage at diagnosis.
引用
收藏
页码:511 / 520
页数:10
相关论文
共 44 条
[31]  
Smida J, 1999, INT J CANCER, V80, P32, DOI 10.1002/(SICI)1097-0215(19990105)80:1<32::AID-IJC7>3.3.CO
[32]  
2-C
[33]   ret/PTC and BRAF act as distinct molecular, time-dependant triggers in a sporadic Irish cohort of papillary thyroid carcinoma [J].
Smyth, P ;
Finn, S ;
Cahill, S ;
O'Regan, E ;
Flavin, R ;
O'Leary, JJ ;
Sheils, O .
INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2005, 13 (01) :1-8
[34]   BRAF mutations and RET/PTC rearrangements are alternative events in the etiopathogenesis of PTC [J].
Soares, P ;
Trovisco, V ;
Rocha, AS ;
Lima, J ;
Castro, P ;
Preto, A ;
Máximo, V ;
Botelho, T ;
Seruca, R ;
Sobrinho-Simoes, M .
ONCOGENE, 2003, 22 (29) :4578-4580
[35]  
Tallini G, 1998, CLIN CANCER RES, V4, P287
[36]   Type and prevalence of BRAF mutations are closely associated with papillary thyroid carcinoma histotype and patients' age but not with tumour aggressiveness [J].
Trovisco, V ;
Soares, P ;
Preto, A ;
de Castro, IV ;
Lima, J ;
Castro, P ;
Máximo, V ;
Botelho, T ;
Moreira, S ;
Meireles, A ;
Magalhas, J ;
Abrosimov, A ;
Cameselle-Teijeiro, J ;
Sobrinho-Simoes, M .
VIRCHOWS ARCHIV, 2005, 446 (06) :589-595
[37]   Prognostic value of [18F]fluorodeoxyglucose positron emission tomographic scanning in patients with thyroid cancer [J].
Wang, WP ;
Larson, SM ;
Fazzari, M ;
Tickoo, SK ;
Kolbert, K ;
Sgouros, G ;
Yeung, H ;
Macapinlac, H ;
Rosai, J ;
Robbins, RJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (03) :1107-1113
[38]  
Weetman A., 2000, WERNER INGBARS THYRO
[39]   BRAF mutation in thyroid cancer [J].
Xing, M .
ENDOCRINE-RELATED CANCER, 2005, 12 (02) :245-262
[40]   The T1799A BRAF mutation is not a germline mutation in familial nonmedullary thyroid cancer [J].
Xing, MZ .
CLINICAL ENDOCRINOLOGY, 2005, 63 (03) :263-266