p53 mutations in chondrosarcoma

被引:44
|
作者
Terek, RM
Healey, JH
Garin-Chesa, P
Mak, S
Huvos, A
Albino, AP
机构
[1] Brown Univ, Sch Med, Rhode Isl Hosp, Dept Orthopaed, Providence, RI USA
[2] Vet Adm Med Ctr, Providence, RI 02908 USA
[3] Cornell Univ, Sch Med, Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[4] Cornell Univ, Sch Med, Mem Sloan Kettering Canc Ctr, Orthopaed Surg Serv, New York, NY 10021 USA
[5] Cornell Univ, Sch Med, Mem Sloan Kettering Canc Ctr, Lab Mammalian Cell Transformat, New York, NY 10021 USA
关键词
bone tumors; tumor suppressor genes; cartilage; chondrosarcoma; p53; single-strand conformational polymorphism;
D O I
10.1097/00019606-199802000-00009
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 a primary bone tumor that has several different grades and variants. We evaluated 48 chondrosarcomas for p53 overexpression and p53 mutations. p53 expression was evaluated with immunohistochemistry using monoclonal antibodies PAb421, PAb1801, and PAb240. p53 mutations were identified with single-strand conformational polymorphism (SSCP) and DNA sequencing in selected cases. Immunohistochemistry revealed nuclear staining with PAb421 and PAb 1801 in the spindle cell portion of one dedifferentiated chondrosarcoma. SSCP analysis was abnormal only in the case with positive immunostaining and localized the mutation to exons 7 and 8. DNA sequence analysis identified a point mutation of G to C in codon 276, resulting in an amino acid substitution of proline for alanine. This point mutation has been reported previously in other tumors but not in chondrosarcoma. Assimilation of our results with previous studies suggests that p53 mutations are present in a minority of chondrosarcomas but when present, are in higher grade chondrosarcomas and their variants.
引用
收藏
页码:51 / 56
页数:6
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