DNA ploidy, nuclear size, proliferation index and DNA-hypomethylation in ovarian cancer

被引:48
作者
Zeimet, Alain G. [1 ,2 ]
Fiegl, Heidi [1 ,2 ]
Goebel, Georg [2 ,3 ]
Kopp, Francis [4 ,5 ]
Allasia, Claude [5 ,6 ]
Reimer, Daniel [1 ,2 ]
Steppan, Ilona [1 ,2 ]
Mueller-Holzner, Elisabeth [1 ,2 ]
Ehrlich, Melanie [7 ,8 ]
Marth, Christian [1 ,2 ]
机构
[1] Innsbruck Med Univ, Dept Gynecol & Obstet, Innsbruck, Austria
[2] Med Univ Innsbruck, Innsbruck, Austria
[3] Innsbruck Med Univ, Dept Med Stat Informat & Hlth Econ, Innsbruck, Austria
[4] Hop Nord Marseille, Fac Med, Histol Lab, Marseille, France
[5] Univ Aix Marseille 2, F-13284 Marseille 07, France
[6] Hop Nord Marseille, Dept Pathol, Marseille, France
[7] Tulane Canc Ctr, Human Genet Program, New Orleans, LA USA
[8] Tulane Med Sch, Dept Biochem, New Orleans, LA USA
关键词
DNA ploidy; Nuclear area; Proliferation index; DNA-hypomethylation; Ovarian cancer; PROGNOSTIC-SIGNIFICANCE; CELL CARCINOMAS; BLADDER-CANCER; METHYLATION; TUMORS; PROGRESSION; CHROMATIN; SURVIVAL; LEUKEMIA; LEVEL;
D O I
10.1016/j.ygyno.2010.12.332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. The present study was undertaken to analyze the impact of epigenetic alterations with a main focus on nuclear area, aneuploidy, hyperploidy, and proliferation in 70 ovarian cancer specimens. Methods. Morphometric changes and somatic chromosomal ploidy status were assessed by Feulgen spectrophotometry. DNA-hypomethylation of LINE1 repeats was analyzed by means of MethyLight PCR, and methylation levels of satellite 2 (Sat2) and satellite alpha (Sat alpha) DNA sequences in chromosome 1 were measured by Southern blot analysis. These parameters were analyzed with regard to correlations as well as to recurrence and survival. Results. We identified a significant association between LINE1 DNA-hypomethylation and patient age (p = 0.029). Furthermore, LINE1 DNA-hypomethylation was positively correlated with the nuclear area (r = 0.47; p < 0.001) and the proliferation index (r = 0.36; p < 0.001). Univariate survival analysis showed that the nuclear area and LINE1 DNA-hypomethylation were prognostic factors for overall (p = 0.015 and = 0.006, respectively) and progression-free survival (p = 0.020 and p = 0.001 respectively), the percentage of aneuploidy only for overall survival (p = 0.031). Subgroup survival analyses revealed that the prognostic value of these factors is strictly confined to mucinous cancers. In serous cancers no prognostic value could be pointed out for any analyzed parameter. Multivariate analysis of the entire cohort showed that the percentage of hyperploidy was an independent prognostic parameter for overall survival (p = 0.003) and LINE1 DNA-hypomethylation for progression-free survival (p = 0.03). In mucinous cancers nuclear area and LINE1 DNA-hypomethylation were found to be independent predictors of progression-free and overall survival. Conclusions. In this study we identified the correlations between early cancer-associated genome DNA-hypomethylation, nuclear morphometric changes, somatic chromosomal ploidy status and the proliferation index. Prognostic relevance of nuclear area and LINE1 DNA-hypomethylation was revealed exclusively in mucinous ovarian cancers. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:24 / 31
页数:8
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