ANALYSIS OF ADENOMATOUS POLYPOSIS-COLI GENE IN THYROID-TUMORS

被引:29
作者
COLLETTA, G
SCIACCHITANO, S
PALMIROTTA, R
RANIERI, A
ZANELLA, E
CAMA, A
COSTANTINI, RM
BATTISTA, P
PONTECORVI, A
机构
[1] IST TUMORI REGINA ELENA, ONCOGENESI MOLEC LAB, I-00158 ROME, ITALY
[2] UNIV ROMA LA SAPIENZA, DEPT EXPTL MED, I-00100 ROME, ITALY
[3] UNIV ROMA TOR VERGATA, DEPT SURG, I-00100 ROME, ITALY
[4] UNIV CATTOLICA SACRO CUORE, INST MED PATHOL, I-00100 ROME, ITALY
[5] UNIV CHIETI, INST HUMAN PATHOL, CHIETI, ITALY
关键词
D O I
10.1038/bjc.1994.452
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Familial adenomatous polyposis (FAP) is known to be associated with neoplasia of various tissues, including thyroid carcinoma. Germline mutations of the tumour-suppressor gene APC, responsible for the predisposition to FAP, may therefore be involved in the pathogenesis of these tumours. In this report the structure of the APC gene has been investigated in 26 thyroid tumours, at different stages of dedifferentiation, that were surgically excised from patients with a negative history of FAP. Approximately 35% of the APC gene coding region, where most of the mutations are clustered, has been analysed by a combination of single-strand conformation polymorphism and direct sequencing. No significant alterations could be demonstrated in any sample examined. It is concluded that, at least in patients not affected by FAP, APC gene abnormalities do not seem to play a relevant role in the pathogenesis of thyroid carcinoma.
引用
收藏
页码:1085 / 1088
页数:4
相关论文
共 45 条
[1]  
ALM T, 1973, CLIN GASTROENTEROL, V2, P577
[2]   FAMILIAL ADENOMATOUS POLYPOSIS (GARDNERS-SYNDROME) AND THYROID-CARCINOMA - A CASE-REPORT AND REVIEW OF THE LITERATURE [J].
BELL, B ;
MAZZAFERRI, EL .
DIGESTIVE DISEASES AND SCIENCES, 1993, 38 (01) :185-190
[3]   PAPILLARY THYROID-CARCINOMA IN DANISH PATIENTS WITH FAMILIAL ADENOMATOUS POLYPOSIS [J].
BULOW, S ;
HOLM, NV ;
MELLEMGAARD, A .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 1988, 3 (01) :29-31
[4]  
CAMA A, 1993, IN PRESS HUM MUTAT
[5]   ASSOCIATION OF THYROID CARCINOMA WITH GARDNERS SYNDROME IN SIBLINGS [J].
CAMIEL, MR ;
MULE, JE ;
ALEXANDER, LL ;
BENNINGHOFF, DL .
NEW ENGLAND JOURNAL OF MEDICINE, 1968, 278 (19) :1056-+
[6]  
CRAIL H W, 1949, U S Nav Med Bull, V49, P123
[7]   THYROID-CARCINOMA IN 2 SISTERS WITH FAMILIAL POLYPOSIS OF THE COLON - CASE-REPORTS AND REVIEW OF THE LITERATURE [J].
DELAMARRE, J ;
CAPRON, JP ;
ARMAND, A ;
DUPAS, JL ;
DESCHEPPER, B ;
DAVION, T .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1988, 10 (06) :659-662
[8]  
DELAMARRE J, 1982, GASTROEN CLIN BIOL, V6, P1016
[9]   GENE P53 MUTATIONS ARE RESTRICTED TO POORLY DIFFERENTIATED AND UNDIFFERENTIATED CARCINOMAS OF THE THYROID-GLAND [J].
DONGHI, R ;
LONGONI, A ;
PILOTTI, S ;
MICHIELI, P ;
DELLAPORTA, G ;
PIEROTTI, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) :1753-1760
[10]   HIGH PREVALENCE OF MUTATIONS OF THE P53 GENE IN POORLY DIFFERENTIATED HUMAN THYROID CARCINOMAS [J].
FAGIN, JA ;
MATSUO, K ;
KARMAKAR, A ;
CHEN, DL ;
TANG, SH ;
KOEFFLER, HP .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) :179-184