COMPARATIVE-STUDY OF P53 GENE AND PROTEIN ALTERATIONS IN HUMAN ASTROCYTIC TUMORS

被引:206
作者
LOUIS, DN
VONDEIMLING, A
CHUNG, RY
RUBIO, MP
WHALEY, JM
EIBL, RH
OHGAKI, H
WIESTLER, OD
THOR, AD
SEIZINGER, BR
机构
[1] MASSACHUSETTS GEN HOSP,DEPT PATHOL,BOSTON,MA 02114
[2] MASSACHUSETTS GEN HOSP,MOLEC NEURORONCOL LAB,BOSTON,MA 02114
[3] MASSACHUSETTS GEN HOSP,NEUROSURG SERV,BOSTON,MA 02114
[4] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[5] UNIV ZURICH,DEPT NEUROPATHOL,CH-8006 ZURICH,SWITZERLAND
关键词
AGE; ASTROCYTOMA; GLIOBLASTOMA MULTIFORME; IMMUNOHISTOCHEMISTRY; P53; GENE; PROTEIN; SEX;
D O I
10.1097/00005072-199301000-00005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The p53 gene is a tumor suppressor gene involved in many common malignancies, including astrocytomas. Genetic analysis of the p53 gene and immunohistochemistry of the p53 protein have each been used to screen astrocytomas. To compare these methods, we performed immunohistochemistry with the monoclonal antibody PAb 1801 and single-strand conformational polymorphism (SSCP) with sequence analysis on 34 astrocytic tumors (WHO grades II, III and IV). Seven cases had detectable p53 protein and gene mutations, while twelve cases had neither detectable protein nor gene mutations. Four tumors had frameshift mutations in the p53 gene that were not revealed by immunohistochemistry. One tumor had a genetic polymorphism and no detectable p53 protein. Ten tumors had p53 protein accumulation but no mutations by SSCP; these cases may represent p53 mutations outside of the conserved exons or elevated levels of wild-type p53 protein. Thus, some p53 mutations are missed with PAb 1801 immunohistochemistry alone. p53 immunohistochemistry, however, may reveal p53 accumulation independent of mutations in the conserved portions of the gene. Finally, we suggest that glioblastomas with p53 mutations in the conserved region of the gene may be a subset that are more common in women and in younger patients.
引用
收藏
页码:31 / 38
页数:8
相关论文
共 57 条
[21]   HORMONE DEPENDENCE OF EXPERIMENTALLY INDUCED GLIOMAS IN RAT [J].
HOPEWELL, JW .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1975, 1 (02) :141-148
[22]   SEX DEPENDENCE OF HUMAN INTRACRANIAL GLIOMATA [J].
HOPEWELL, JW ;
EDWARDS, DN ;
WIERNIK, G .
BRITISH JOURNAL OF CANCER, 1976, 34 (06) :666-670
[23]   INCREASED EXPRESSION OF MUTANT FORMS OF P53 ONCOGENE IN PRIMARY LUNG-CANCER [J].
IGGO, R ;
GATTER, K ;
BARTEK, J ;
LANE, D ;
HARRIS, AL .
LANCET, 1990, 335 (8691) :675-679
[24]   NUCLEAR P53 IMMUNOREACTION ASSOCIATED WITH POOR PROGNOSIS OF BREAST-CANCER [J].
IWAYA, K ;
TSUDA, H ;
HIRAIDE, H ;
TAMAKI, K ;
TAMAKUMA, S ;
FUKUTOMI, T ;
MUKAI, K ;
HIROHASHI, S .
JAPANESE JOURNAL OF CANCER RESEARCH, 1991, 82 (07) :835-840
[25]  
JAROS E, 1991, Neuropathology and Applied Neurobiology, V17, P522
[26]   IDENTIFICATION OF P53 AS A SEQUENCE-SPECIFIC DNA-BINDING PROTEIN [J].
KERN, SE ;
KINZLER, KW ;
BRUSKIN, A ;
JAROSZ, D ;
FRIEDMAN, P ;
PRIVES, C ;
VOGELSTEIN, B .
SCIENCE, 1991, 252 (5013) :1708-1711
[27]  
KLEIHUES P, 1992, IN PRESS HISTOLOGICA
[28]   CHARACTERIZATION OF THE HUMAN P53-GENE [J].
LAMB, P ;
CRAWFORD, L .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (05) :1379-1385
[29]  
LEHMAN TA, 1991, CANCER RES, V51, P4090
[30]   THE P53 TUMOR SUPPRESSOR GENE [J].
LEVINE, AJ ;
MOMAND, J ;
FINLAY, CA .
NATURE, 1991, 351 (6326) :453-456