Romei Cristina, Ciampi Raffaele, Faviana Pinuccia, Agate Laura, Molinaro Eleonora, Bottici Valeria, Basolo Fulvio, Miccoli Paolo, Pacini Furio, Pinchera Aldo, Elisei Rossella
Departments of Endocrinology and Metabolism Oncology Surgery, University of Pisa, 56100 Pisa, Italy.
Endocr Relat Cancer. 2008 Jun;15(2):511-20. doi: 10.1677/ERC-07-0130.
A low sodium iodide symporter (NIS) expression has been shown in papillary thyroid carcinomas (PTCs) harboring the BRAFV600E 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 BRAFV600E or RET/PTC rearrangements. We found BRAFV600E 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 BRAFV600E-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 BRAFV600E-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-1 and GLUT-3 mRNA expression was considered, no correlation was found either in BRAFV600E- 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 BRAFV600E 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 BRAFV600E-mutated PTC, thus suggesting that the previously demonstrated poor prognostic significance of BRAFV600E mutation could be related to the dedifferentiation process more than to a more advanced stage at diagnosis.
在携带BRAFV600E突变的甲状腺乳头状癌(PTC)中已显示出低钠碘同向转运体(NIS)表达。在本研究中,我们根据BRAFV600E或RET/PTC重排的存在情况,分析了78例PTC中甲状腺分化基因、葡萄糖转运蛋白(GLUT)-1和GLUT-3的mRNA表达。我们分别在35.8%和19.4%的PTC中发现了BRAFV600E和RET/PTC重排。与未突变样本相比,BRAFV600E阳性PTC中NIS和甲状腺过氧化物酶(TPO)基因的mRNA表达显著降低(分别为P<0.0001和P=0.004)。支持这一结果的是,免疫组织化学显示,BRAFV600E突变的PTC中NIS阳性细胞的百分比(平均53.5%)显著低于阴性病例(平均72.6%)(P=0.005)。相比之下,有或无RET/PTC重排的PTC在NIS或任何其他甲状腺分化基因的mRNA表达上均未发现差异。当考虑GLUT-1和GLUT-3的mRNA表达时,在BRAFV600E或RET/PTC突变病例中均未发现相关性。总之,本研究证实64%的PTC病例中存在BRAF和/或RET癌基因的基因改变,并揭示BRAFV600E突变与NIS和TPO的低表达显著相关。后一发现可能表明,BRAFV600E突变的PTC在分子水平上存在早期去分化过程,因此表明先前证明的BRAFV600E突变的不良预后意义可能更多地与去分化过程有关,而不是与诊断时更晚期的阶段有关。