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[原发性前列腺癌的细胞遗传学研究]

[Cytogenetic investigations in primary prostate carcinomas].

作者信息

Szücs S, Zitzelsberger H, Roter M, Bauchinger M, Höfler H

机构信息

Institut für Allgemeine Pathologie und Pathologische Anatomie der Technischen Universität München Klinikum rechts der Isar.

出版信息

Verh Dtsch Ges Pathol. 1993;77:138-41.

PMID:7511272
Abstract

Primary cultures of 48 cases of prostate carcinoma were established. The expression of cytokeratin and prostate specific antigen were determined in the cultures routinely. G-banding analysis revealed some clonal numerical and structural aberrations: Trisomy 7 occurred in 4 cases, in one case in combination with a t(Y;22). Loss of the Y chromosome was found in 3 cases, in one case in combination with gain of chromosome #5. The most frequent clonal structural aberration var9(qh) occurred in 6 cases. A deletion of 6q(23) was found in two cases. None of these aberrations were found in normal tissue of the same patients. Numerical changes were demonstrated by fluorescence in situ hybridization (FISH) on native tissue, confirming the conventional cytogenetic findings.

摘要

建立了48例前列腺癌的原代培养物。常规检测培养物中细胞角蛋白和前列腺特异性抗原的表达。G显带分析显示出一些克隆性数目和结构异常:7号染色体三体在4例中出现,其中1例伴有t(Y;22)。Y染色体缺失在3例中发现,其中1例伴有5号染色体增加。最常见的克隆性结构异常var9(qh)在6例中出现。2例发现6q(23)缺失。在同一患者的正常组织中未发现这些异常。通过对天然组织进行荧光原位杂交(FISH)证实了数目变化,确认了传统细胞遗传学的发现。

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