Iodide symporter gene expression in human thyroid tumors

被引:143
作者
Arturi, F
Russo, D
Schlumberger, M
du Villard, JA
Caillou, B
Vigneri, P
Wicker, R
Chiefari, E
Suarez, HG
Filetti, S
机构
[1] Univ Catanzaro, Dipartimento Med Sperimentale & Clin, Cattedra Endocrinol, I-88100 Catanzaro, Italy
[2] Univ Catanzaro, Fac Farm, Cattedra Farmacol, I-88100 Catanzaro, Italy
[3] Ist Nazl Tumori, I-20133 Milan, Italy
[4] CNRS, Inst Rech Sci Canc, F-94802 Villejuif, France
[5] Inst Gustave Roussy, F-94805 Villejuif, France
关键词
D O I
10.1210/jc.83.7.2493
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Expression of the Na/+I- symporter (NIS) gene was investigated by RT-PCR in a selected series of 26 primary thyroid carcinomas (19 papillary, 5 follicular, and 2 anaplastic). Fifteen follicular adenomas (11 "cold " and 4 "hot" adenomas) were also studied. Five of 19 papillary thyroid cancer did not express NIS messenger ribonucleic acid (mRNA). In all but 1 follicular cancer, NIS transcript was fully detected. In anaplastic tissue, NIS mRNA was only barely detected in 1 case. All of the follicular thyroid adenomas except 1 expressed the NIS gene. In contrast, all tumors studied excluding the anaplastic histotype fully expressed thyroglobulin and thyroid peroxidase mRNA transcripts. In 2 patients, a lower expression (3- to 5-fold) of NIS mRNA was found in metastasis by dot blot analysis compared with those in both normal and primary neoplastic thyroid tissue. Four of 8 differentiated thyroid cancer patients selected for the presence of metastases with negative posttherapy I-131 total body scan showed the lack of NIS gene expression in their primary cancer. This defect, at least in these cases, is a somatic and intrinsic lesion of the primary cancer cells and is not due to a dedifferentiation process in the metastatic tissue. The early detection of the loss of NIS gene expression in the primary cancer, therefore, may provide useful information for the management of differentiated thyroid cancer patients.
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页码:2493 / 2496
页数:4
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