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人类睾丸生殖细胞肿瘤中选定的肿瘤抑制基因杂合性缺失。

Loss of heterozygosity of selected tumor suppressor genes in human testicular germ cell tumors.

机构信息

Department of Biochemical Engineering, Faculty of Food Technology and Biotechnology, University of Zagreb, Zagreb, Croatia.

出版信息

Pathol Res Pract. 2010 Mar 15;206(3):163-7. doi: 10.1016/j.prp.2009.10.007. Epub 2010 Jan 25.

Abstract

Human testicular germ cell tumors (TGCTs) are histologically heterogenous neoplasms with a variable malignant potential. Two main groups of germ cell tumors occur in men: seminomas and nonseminomas. In the present study, a set of four tumor suppressor genes was investigated in testicular cancers. CDH1, APC, p53, and nm23-H1 genes were tested for loss of heterozygosity (LOH). Thirty-eight testicular germ cell tumors (17 seminomas and 21 nonseminomas) were analyzed by PCR using restriction fragment length polymorphism or the dinucleotide/tetranucleotide repeat polymorphism method. An allelic loss of p53 at exon 4 was detected in five nonseminomas, whereas LOH of p53 at intron 6 occurred in one of the seminoma and two of the nonseminoma samples. Allelic losses of the APC gene were present in three seminomas and one nonseminoma, whereas one seminoma and three nonseminomas showed LOH of CDH1. The analysis of allelic losses showed no common structural genetic alterations in tumor tissues, although a different pattern of LOH was observed between the two main histological groups of TGCTs.

摘要

人类睾丸生殖细胞肿瘤 (TGCTs) 是组织学上具有异质性的肿瘤,具有不同的恶性潜能。两种主要的睾丸生殖细胞肿瘤发生在男性中:精原细胞瘤和非精原细胞瘤。在本研究中,研究了一组四个肿瘤抑制基因在睾丸癌中的变化。使用 PCR 结合限制片段长度多态性或二核苷酸/四核苷酸重复多态性方法检测 CDH1、APC、p53 和 nm23-H1 基因的杂合性丢失 (LOH)。对 38 例睾丸生殖细胞肿瘤(17 例精原细胞瘤和 21 例非精原细胞瘤)进行了分析。在 5 例非精原细胞瘤中检测到 p53 外显子 4 的等位基因丢失,而在 1 例精原细胞瘤和 2 例非精原细胞瘤样本中检测到 p53 内含子 6 的 LOH。在 3 例精原细胞瘤和 1 例非精原细胞瘤中存在 APC 基因的等位基因丢失,而 1 例精原细胞瘤和 3 例非精原细胞瘤显示 CDH1 的 LOH。虽然在 TGCTs 的两个主要组织学组之间观察到不同的 LOH 模式,但对肿瘤组织的分析显示没有共同的结构遗传改变。

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