The sodium/iodide symporter (NIS):: Characterization, regulation, and medical significance

被引:652
作者
Dohán, O [1 ]
De la Vieja, A [1 ]
Paroder, V [1 ]
Riedel, C [1 ]
Artani, M [1 ]
Reed, M [1 ]
Ginter, CS [1 ]
Carrasco, N [1 ]
机构
[1] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10461 USA
关键词
D O I
10.1210/er.2001-0029
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The Na+/I- symporter (NIS) is an integral plasma membrane glycoprotein that mediates active I- transport into the thyroid follicular cells, the first step in thyroid hormone biosynthesis. NIS-mediated thyroidal I- transport from the bloodstream to the colloid is a vectorial process made possible by the selective targeting of NIS to the basolateral membrane. NIS also mediates active I- transport in other tissues, including salivary glands, gastric mucosa, and lactating mammary gland, in which it translocates I- into the milk for thyroid hormone biosynthesis by the nursing newborn. NIS provides the basis for the effective diagnostic and therapeutic management of thyroid cancer and its metastases with radioiodide. NIS research has proceeded at an astounding pace after the 1996 isolation of the rat NIS cDNA, comprising the elucidation of NIS secondary structure and topology, biogenesis and posttranslational modifications, transcriptional and posttranscriptional regulation, electrophysiological analysis, isolation of the human NIS cDNA, and determination of the human NIS genomic organization. Clinically related topics include the analysis of congenital I- transport defect-causing NIS mutations and the role of NIS in thyroid cancer. NIS has been transduced into various kinds of cancer cells to render them susceptible to destruction with radioiodide. Most dramatically, the discovery of endogenous NIS expression in more than 80% of human breast cancer samples has raised the possibility that radioiodide may be a valuable novel tool in breast cancer diagnosis and treatment.
引用
收藏
页码:48 / 77
页数:30
相关论文
共 242 条
[1]
IDENTIFICATION OF A MUTATION IN THE CODING SEQUENCE OF THE HUMAN THYROID PEROXIDASE GENE CAUSING CONGENITAL GOITER [J].
ABRAMOWICZ, MJ ;
TARGOVNIK, HM ;
VARELA, V ;
COCHAUX, P ;
KRAWIEC, L ;
PISAREV, MA ;
PROPATO, FVE ;
JUVENAL, G ;
CHESTER, HA ;
VASSART, G .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (04) :1200-1204
[2]
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland [J].
Abramowicz, MJ ;
Duprez, L ;
Parma, J ;
Vassart, G ;
Heinrichs, C .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :3018-3024
[3]
Detection of binding and blocking autoantibodies to the human sodium-iodide symporter in patients with autoimmune thyroid disease [J].
Ajjan, RA ;
Kemp, EH ;
Waterman, EA ;
Watson, PF ;
Endo, T ;
Onaya, T ;
Weetman, AP .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (05) :2020-2027
[4]
Regulation and tissue distribution of the human sodium iodide symporter gene [J].
Ajjan, RA ;
Kamaruddin, NA ;
Crisp, M ;
Watson, PF ;
Ludgate, M ;
Weetman, AP .
CLINICAL ENDOCRINOLOGY, 1998, 49 (04) :517-523
[5]
The sodium iodide symporter gene and its regulation by cytokines found in autoimmmunity [J].
Ajjan, RA ;
Watson, PF ;
Findlay, C ;
Metcalfe, RA ;
Crisp, M ;
Ludgate, M ;
Weetman, AP .
JOURNAL OF ENDOCRINOLOGY, 1998, 158 (03) :351-358
[6]
The modulation of the human sodium iodide symporter activity by Graves' disease sera [J].
Ajjan, RA ;
Findlay, C ;
Metcalfe, RA ;
Watson, PF ;
Crisp, M ;
Ludgate, M ;
Weetman, AP .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (04) :1217-1221
[7]
ALALAWI N, 1995, MOL CELL BIOL, V15, P1162
[8]
CONGENITAL HYPOTHYROIDISM FROM COMPLETE IODIDE TRANSPORT DEFECT - LONG-TERM EVOLUTION WITH IODIDE TREATMENT [J].
ALBERO, R ;
CERDAN, A ;
FRANCO, FS .
POSTGRADUATE MEDICAL JOURNAL, 1987, 63 (746) :1043-1047
[9]
[Anonymous], 1923, J AM MED ASS
[10]
ARMSTRONG R, 1995, MOL CELL BIOL, V15, P1826