Status and expression of the p16(INK)4 gene in human thyroid tumors and thyroid-tumor cell lines

被引:0
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作者
Calabro, V
Strazzullo, M
LaMantia, G
Fedele, M
Paulin, C
Fusco, A
Lania, L
机构
[1] UNIV NAPLES FEDERICO II,FAC SCI,DIPARTIMENTO GENET BIOL GEN & MOLEC,I-80134 NAPLES,ITALY
[2] IST NAZL TUMORI FDN PASCLAE,I-80131 NAPLES,ITALY
[3] CTR HOSP LYON SUD,LAB HISTOL & CYTOL,F-69600 OULLINS,FRANCE
[4] UNIV REGGIO CALABRIA,DIPARTIMENTO MED SPERIMENTALE & CLIN,I-88100 CATANZARO,ITALY
关键词
D O I
10.1002/(SICI)1097-0215(19960703)67:1<29::AID-IJC7>3.0.CO;2-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The p16(INK4) tumor-suppressor gene (also known as CDKN2, CDK41 and MTS1) encodes a negative regulator of the cell cycle. This gene, located in 9p21, is mutated or homozygously deleted in a high percentage of tumor cell lines and specific types of primary tumors. We have examined the status of the p16(INK4) gene in 31 thyroid tumors and 7 thyroid cell liner. No DNA abnormalities were found in primary tumors. Conversely, p16(INK4) gene structural alterations, deletions and point mutations were found in 4 thyroid cell lines. The expression of the 2 different p16(INK4) mRNAs, the p16 alpha and p16 beta transcripts, was determined by RNA-PCR experiments. All the primary thyroid tumors expressed the beta transcript, while the p16 alpha was barely detectable. The thyroid cell lines always expressed the p16 beta transcript, while the a transcript was absent or, whenever present, coded for a mutated form of the p16(INK4) gene product. Taken together, our results suggest that loss of p16(INK4) function is not directly involved in the process of thyroid-tumor development, but it probably gives cells in tissue culture a selective growth advantage. (C) 1996 Wiley-Liss, Inc.
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页码:29 / 34
页数:6
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