Thyroid papillary carcinoma:: preliminary evidence for a germ-line single nucleotide polymorphism in the Fas gene

被引:15
作者
Basolo, F
Giannini, R
Faviana, P
Fontanini, G
Malizia, AP
Ugolini, C
Elisei, R
Miccoli, P
Toniolo, A
机构
[1] Univ Pisa, Dipartimento Oncol, I-56126 Pisa, Italy
[2] Univ Pisa, Dipartimento Chirurg, I-56126 Pisa, Italy
[3] Univ Pisa, Dipartimento Endocrinol & Metab, I-56124 Pisa, Italy
[4] Univ Insubria, Dipartimento Sci Clin & Biol, I-21100 Varese, Italy
关键词
D O I
10.1677/joe.0.1820479
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The expression of Fas in thyroid tumours and Graves' disease was analysed by mRNA transcript expression. As compared with unaffected thyroid tissue, Fas expression was enhanced in Graves' disease, adenomas, and papillary and follicular carcinomas. This pattern was also reflected in immunohistochemical studies. The PCR single-strand conformational polymorphism (SSCP) method and DNA sequencing were used to analyse Fas exons 1-9. The study was carried out on five different histotypes of thyroid tumours (n = 93) and tissue from Graves' disease patients. As compared with a group of healthy blood donors (n = 64), a significant association (P = 0.006) emerged between papillary thyroid carcinoma and a silent single nucleotide polymorphism (SNP, 988C-->T) in exon 7 of the Fas gene. Other forms of thyroid pathology were not associated with the above polymorphism. Patients with neoplasia showed the same SNP in turnout tissue, in the unaffected contralateral thyroid lobe, and in peripheral blood cells. Thus, the 988C-->T polymorphism appeared to be of germ-line origin.
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页码:479 / 484
页数:6
相关论文
共 41 条
[1]   Fas (CD95) expression is up-regulated on papillary thyroid carcinoma [J].
Arscott, PL ;
Stokes, T ;
Myc, A ;
Giordano, TJ ;
Thompson, NW ;
Baker, JR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (11) :4246-4252
[2]   Suppression of Fas expression and down-regulation of Fas ligand in highly aggressive human thyroid carcinoma [J].
Basolo, F ;
Fiore, L ;
Baldanzi, A ;
Giannini, R ;
Dell'Omodarme, M ;
Fontanini, G ;
Pacini, F ;
Danesi, R ;
Miccoli, P ;
Toniolo, A .
LABORATORY INVESTIGATION, 2000, 80 (09) :1413-1419
[3]   Mutation analysis of CD95 (APO-1/Fas) in childhood B-lineage acute lymphoblastic leukaemia [J].
Beltinger, C ;
Böhler, T ;
Karawajew, L ;
Ludwig, WD ;
Schrappe, M ;
Debatin, KM .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 102 (03) :722-728
[4]   Lack of CD95/FAS gene somatic mutations in extranodal, nodal and splenic marginal zone B cell lymphomas [J].
Bertoni, F ;
Conconi, A ;
Luminari, S ;
Realini, C ;
Roggero, E ;
Baldini, L ;
Carobbio, S ;
Cavalli, F ;
Neri, A ;
Zucca, E .
LEUKEMIA, 2000, 14 (03) :446-448
[5]  
Boldrini L, 2002, INT J ONCOL, V20, P155
[6]  
Bolstad AI, 2000, J RHEUMATOL, V27, P2397
[7]  
CHENG JH, 1995, J IMMUNOL, V154, P1239
[8]   Fas and Fas ligand gene mutations in Hashimoto's thyroiditis [J].
Dong, ZM ;
Takakuwa, T ;
Takayama, H ;
Luo, WJ ;
Takano, T ;
Amino, N ;
Matsuzuka, F ;
Aozasa, K .
LABORATORY INVESTIGATION, 2002, 82 (12) :1611-1616
[9]   Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome [J].
Eriksson, M ;
Brown, WT ;
Gordon, LB ;
Glynn, MW ;
Singer, J ;
Scott, L ;
Erdos, MR ;
Robbins, CM ;
Moses, TY ;
Berglund, P ;
Dutra, A ;
Pak, E ;
Durkin, S ;
Csoka, AB ;
Boehnke, M ;
Glover, TW ;
Collins, FS .
NATURE, 2003, 423 (6937) :293-298
[10]   Many cuts to ruin:: a comprehensive update of caspase substrates [J].
Fischer, U ;
Jänicke, RU ;
Schulze-Osthoff, K .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (01) :76-100