PTEN mutation is rare in chondrosarcoma

被引:20
作者
Lin, CZ [1 ]
Meitner, PA [1 ]
Terek, RM [1 ]
机构
[1] Brown Univ, Sch Med, Dept Orthopaed, Providence, RI 02912 USA
关键词
bone tumor; chondrosarcoma; PTEN; tumor suppressor gene;
D O I
10.1097/00019606-200203000-00005
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
Chondrosarcoma is the second most common primary malignant neoplasm of bone in adults. but the major genetic events invoked in the progression of this often-fatal cancer remain to he elucidated. Loss of heterozygosity of chromosome 10q has been reported in 67% of chondrosarcoma. The tumor suppressor gene PTEN is located on chromosome 10q, specifically 10q23, raising the possibility that the loss of PTEN function is responsible for some chondrosarcomas. The authors examined 40 chondrosarcoma tumors and tumor-derived cell lines for alterations in PTEN. Only one mutation resulting in a truncated PTEN protein was detected, which was in a metastasized extraskeletal myxoid chondrosarcoma. Thus, mutated PTEN is an uncommon event in the development of chondrosarcoma. The high frequency of loss of heterozygosity on 10q suggests the presence of additional tumor suppressor genes at these loci.
引用
收藏
页码:22 / 26
页数:5
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