Genotype-phenotype correlation in gemistocytic astrocytomas

被引:0
|
作者
Kösel, S
Scheithauer, BW
Graeber, MB
机构
[1] Max Planck Inst Neurobiol, Dept Neuromorphol, Martinsried, Germany
[2] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
关键词
astrocytoma; gemistocytes; p53; phenotype; polymerase chain reaction;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: Gemistocytic astrocytomas often behave aggressively and carry the least favorable prognosis among diffuse astrocytomas. The frequency of p53 mutations has been reported to be significantly higher in the gemistocytic variant as compared with other astrocytomas. METHODS: Between 1985 and 1998, we selected 25 tumor samples from among 201 samples from patients with gemistocytic astrocytomas operated on at the Mayo Clinic. Exons 5 to 8 of the p53 gene were sequenced using an automated deoxyribonucleic acid sequencer. Morphometric characterization of individual gemistocytes was performed using an image analysis program. RESULTS: Of 25 tissue samples analyzed, 16 were found to carry a p53 missense mutation (three in exon 5, three in exon 6, one in exon 7, and nine in exon 8), and one sequence variant was synonymous. Mutations were clustered at codons 151 (2 of 17 mutations), 193 (3 of 17 mutations), and 273 (5 of 17 mutations) of the p53 gene. Patients whose tumors carried a p53 mutation were significantly younger than other patients, and their tumors tended to accumulate more p53 protein than those of other patients. Phenotype analysis of gemistocytes revealed that the sizes of tumor cell nuclei and of entire tumor cells in the same tissue area were positively correlated. Smaller tumor cell nuclei tended to be less circular or more atypical. In addition, more atypical gemistocytes were found in tumors lacking a wild-type p53 allele as well as in tissue from patients whose postoperative survival was shorter. CONCLUSION: Our data confirm that the frequency of p53 mutations is significantly higher (approximately twofold) in gemistocytic astrocytomas as compared with other astrocytoma subtypes. Whether the high frequency of p53 mutations contributes to the more aggressive behavior of gemistocytic astrocytomas, however, remains unclear.
引用
收藏
页码:187 / 193
页数:7
相关论文
共 50 条
  • [31] GENOTYPE-PHENOTYPE CORRELATION IN A PEDIATRIC ADPKD COHORT
    Van Giel, Dorien
    De Rechter, Stephanie
    Breysem, Luc
    Hindryckx, An
    Janssens, Peter
    Decuypere, Jean-Paul
    Bammens, Bert
    Corveleyn, Anniek
    Ferec, Claude
    Vennekens, Rudi
    Audrezet, Marie-Pierre
    Harris, Peter
    Mekahli, Djalila
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2020, 35 : 257 - 257
  • [32] Assessment of genotype-phenotype correlation in children with pseudohypoparathyroidism
    Roztoczynska, Dorota
    Preizner-Rzucidlo, Ewelina
    Corica, Domenico
    Janus, Dominika
    Janeczko, Magdalena
    Anna, Wedrychowicz
    Ossowska, Magdalena
    Malgorzata, Wasniewska
    Starzyk, Jarzy
    HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 424 - 425
  • [33] Genotype-phenotype correlation in mitochondrial optic neuropathies
    Verny, Christophe
    Amati-Bonneau, Patrizia
    Ferre, Marc
    Barth, Magalie
    Guillet, Virginie
    Chevrollier, Arnaud
    Malthierry, Yves
    Dubas, Frederic
    Bonneau, Dominique
    Reynier, Pascal
    NEUROLOGY, 2007, 68 (12) : A304 - A304
  • [34] Huntington disease in children: Genotype-phenotype correlation
    Rasmussen, A
    Macias, R
    Yescas, P
    Ochoa, A
    Davila, G
    Alonso, E
    NEUROPEDIATRICS, 2000, 31 (04) : 190 - 194
  • [35] NOVEL METHODS FOR GENOTYPE-PHENOTYPE CORRELATION IN SCHWANNOMATOSIS
    Jordan, Justin
    Smith, Miriam
    Merker, Vanessa
    Cai, Wenli
    Harris, Gordon
    Bredella, Miriam
    Erdin, Serkan
    Gusella, James
    Plotkin, Scott
    NEURO-ONCOLOGY, 2016, 18 : 138 - 138
  • [36] Genotype-phenotype correlation in a French cohort of aniridia
    Bremond-Gignac, Dominique
    ACTA OPHTHALMOLOGICA, 2019, 97
  • [37] Evidence for genotype-phenotype correlation for OTOF mutations
    Yildirim-Baylan, Muzeyyen
    Bademci, Guney
    Duman, Duygu
    Ozturkmen-Akay, Hatice
    Tokgoz-Yilmaz, Suna
    Tekin, Mustafa
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2014, 78 (06) : 950 - 953
  • [38] Genotype-phenotype correlation in spinocerebellar ataxias (SCA)
    Klockgether, T
    Dichgans, J
    CLINICAL NEUROPHYSIOLOGY: FROM RECEPTORS TO PERCEPTION, 1999, 50 : 195 - 201
  • [39] Genotype-Phenotype Correlation in Primary Carnitine Deficiency
    Rose, Emily C.
    di San Filippo, Cristina Amat
    Erlingsson, Uzochi C. Ndukwe
    Ardon, Orly
    Pasquali, Marzia
    Longo, Nicola
    HUMAN MUTATION, 2012, 33 (01) : 118 - 123
  • [40] Genotype-phenotype correlation analysis in GNE myopathy
    Pogoryelova, O.
    Cammish, P.
    Mansbach, H.
    Lochmuller, H.
    NEUROMUSCULAR DISORDERS, 2017, 27 : S41 - S41