Cyclin E gene (CCNE) amplification and hCDC4 mutations in endometrial carcinoma

被引:53
作者
Cassia, R
Moreno-Bueno, G
Rodríguez-Perales, S
Hardisson, D
Cigudosa, JC
Palacios, J
机构
[1] Ctr Nacl Invest Oncol, Lab Breast & Gynaecol Canc, Mol Pathol Programme, Madrid 28029, Spain
[2] Ctr Nacl Invest Oncol, Cytogenet Unit, Madrid 28029, Spain
[3] Hosp Univ La Paz, Dept Pathol, Madrid, Spain
关键词
endometrial carcinoma; cyclin E; cyclin E amplification; hCDC4; mutations;
D O I
10.1002/path.1474
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclin E overexpression occurs in a subset of endometrial carcinomas (ECs), but the molecular mechanisms underlying this alteration remain to be established. The present study has analysed amplification of the cyclin E gene (CCNE) and mutation in hCDC4, the gene coding for the F-box protein, which tags phosphorylated cyclin E for proteosomal degradation, to ascertain whether these alterations might be responsible for cyclin E overexpression in ECs. Cyclin E and p53 expression was studied by immunohistochemistry in eight atypical endometrial hyperplasias (AEHs), 51 endometrioid endometrial carcinomas (EECs), and 22 non-endometrioid endometrial carcinomas (NEECs). CCNE amplification was analysed by fluorescence in situ hybridization (FISH). Mutations in exons 2-11 of the hCDC4 gene were screened by PCR-SSCP-sequencing. Finally, the polymorphic marker D4S1610 was used to assess loss of heterozygosity (LOH) in the hCDC4 gene. Cyclin E overexpression was found in 26/81 (32%) cases and was associated with the histological type of the lesion, since it was not found in any AEHs but was present in 27% of EECs and 54.5% of NEECs (p = 0.035). Cyclin E overexpression was associated with histological grade (p = 0.011) and p53 immunostaining in EECs (p = 0.033). CCNE amplification was found in 6 of 37 (16%) ECs examined. There was a significant association between CCNE amplification and the histological type of the lesion, since five (83%) of the six cases with amplification were NEECs (p = 0.008). One EEC harboured an hCDC4 mutation: a CGA to CAA (Arg/Gln) change at codon 479. In addition, D4S1610 LOH was found in 7 of 23 (30%) informative cases analysed, but no correlation with cyclin E overexpression was found. However, the tumour with hCDC4 mutation also showed LOH. This is the first study demonstrating that cyclin F overexpression is associated with gene amplification in ECs, these alterations being more frequent in NEECs. Although hCDC4 exhibits a low mutation frequency in ECs overexpressing cyclin E, it seems to function as a tumour suppressor gene that is involved in endometrial carcinogenesis. Copyright (C) 2003 John Wiley Sons, Ltd.
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页码:589 / 595
页数:7
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