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前列腺腺癌中的DNA异质性。一项对前列腺全器官切片进行的DNA流式细胞术图谱研究。

DNA heterogeneity in prostatic adenocarcinoma. A DNA flow cytometric mapping study with whole organ sections of prostate.

作者信息

O'Malley F P, Grignon D J, Keeney M, Kerkvliet N, McLean C

机构信息

Department of Pathology, Victoria Hospital, University of Western Ontario, London, Canada.

出版信息

Cancer. 1993 May 1;71(9):2797-802. doi: 10.1002/1097-0142(19930501)71:9<2797::aid-cncr2820710918>3.0.co;2-d.

Abstract

BACKGROUND

The degree of DNA heterogeneity varies between tumors arising at different sites. The presence of a significant degree of variability within a given tumor may result in problems in the interpretation of DNA flow cytometric findings. This study evaluated the degree of DNA heterogeneity in prostatic adenocarcinoma.

METHODS

A total of 122 3-mm punch biopsy specimens were evaluated from single representative whole organ sections from nine cases of prostate cancer (range, 4-18 samples per case; mean, 12 samples; median, 14 samples). Individual punch biopsy specimens were graded and reviewed to confirm the presence of carcinoma and processed for DNA ploidy analysis.

RESULTS

Assessable histograms, defined as having a coefficient of variation of the diploid G0/G1 peak of 7.5% or less, were available for 111 (91%) of the samples. Of the nine cases studied, five (56%) showed heterogeneity in the DNA pattern (diploid plus aneuploid, n = 1; diploid plus tetraploid, n = 2; and diploid plus tetraploid plus aneuploid, n = 2). All four cases having a homogeneous DNA content were DNA diploid in all samples. In those cases with a heterogeneous pattern, the areas having abnormal DNA patterns could not be predicted by histologic pattern or grade.

CONCLUSIONS

From this study, the authors conclude that a significant degree of DNA heterogeneity exists within individual cases of prostatic adenocarcinoma, and this may be an important confounding factor in DNA ploidy studies.

摘要

背景

不同部位发生的肿瘤之间,DNA异质性程度存在差异。给定肿瘤内存在显著程度的变异性可能会导致DNA流式细胞术检测结果解读方面的问题。本研究评估了前列腺腺癌中的DNA异质性程度。

方法

从9例前列腺癌患者的单个代表性全器官切片中获取了总共122个3毫米的穿刺活检标本(范围为每个病例4 - 18个样本;平均12个样本;中位数14个样本)。对各个穿刺活检标本进行分级并复查以确认癌的存在,然后进行DNA倍体分析处理。

结果

111个(91%)样本可获得可评估的直方图,定义为二倍体G0/G1峰的变异系数为7.5%或更低。在研究的9例病例中,5例(56%)显示出DNA模式的异质性(二倍体加非整倍体,n = 1;二倍体加四倍体,n = 2;二倍体加四倍体加非整倍体,n = 2)。所有4例DNA含量均一的病例在所有样本中均为DNA二倍体。在那些具有异质性模式的病例中,具有异常DNA模式的区域无法通过组织学模式或分级来预测。

结论

作者从本研究得出结论,前列腺腺癌的个体病例中存在显著程度的DNA异质性,这可能是DNA倍体研究中的一个重要混杂因素。

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