Molecular alterations of the RB1, TP53, and MDM2 genes in primary and xenografted human osteosarcomas

被引:23
|
作者
Pellin, A
Boix-Ferrero, J
Carpio, D
Lopez-Terrada, D
Carda, C
Navarro, S
Peydro-Olaya, A
Triche, TJ
Llombart-Bosch, A
机构
[1] Univ Valencia, Sch Med, Dept Pathol, Valencia 46010, Spain
[2] Univ So Calif, Childrens Hosp, Dept Pathol, Los Angeles, CA 90027 USA
关键词
RB1; TP53; MDM2; osteosarcomas; exon duplication; exon loss; mutation; amplification; polymorphism; polymerase chain reaction; single strand conformational polymorphism; immunohistochemistry;
D O I
10.1097/00019606-199712000-00005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the status of the RB1, TP53, and MDM2 genes in human osteosarcomas and cell lines established from surgical specimens and transplanted into athymic naked mice. By using reverse transcriptase-polymerase chain reaction (RT-FCR) as a prescreening technique and posterior sequencing, we observe new mutations in the RB1 gene, notably a duplication in tan dem of exons 3 through 6. TP53 mutations appear in codons most frequently mutated in osteosarcomas. We have not seer MDM2 gene amplification in any reported case. These molecular alterations appear in different osteosarcomas not simultaneously present in the same tumor sample. A link has been described between these three genes in the pathways that control the cell cycle and the tumoral progression, but their functions are probably independent in the development of osteosarcomas. TP53 mutations appear in adult patients, whereas RB1 alterations occur mostly in younger patients.
引用
收藏
页码:333 / 341
页数:9
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