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腮腺黏液表皮样癌显示唯一的染色体异常为易位(3;8)(p21;q12)和缺失(5)(q22)。

Mucoepidermoid tumor of the parotid gland showing a translocation (3;8)(p21;q12) and a deletion (5)(q22) as sole chromosome abnormalities.

作者信息

Bullerdiek J, Vollrath M, Wittekind C, Caselitz J, Bartnitzke S

机构信息

Centre of Human Genetics and Genetic Counselling, University of Bremen, F.R.G.

出版信息

Cancer Genet Cytogenet. 1990 Nov 1;50(1):161-4. doi: 10.1016/0165-4608(90)90250-e.

Abstract

The cytogenetic findings in a mucoepidermoid tumor of the parotid gland are described. In addition to a t(3;8)(p21;q12), all cells analyzed showed a deletion of part of the long arm of chromosome 5. Although the typical translocation of benign pleomorphic adenomas was found, histologic examination did not show remnants of a pleomorphic adenoma. Nevertheless, we assumed that the malignant tumor most likely arose in a preexisting pleomorphic adenoma. As a mechanism for malignant transformation, the loss of a suppressor gene located on the long arm of chromosome 5 is discussed.

摘要

本文描述了一例腮腺黏液表皮样癌的细胞遗传学研究结果。除了t(3;8)(p21;q12)外,所有分析的细胞均显示5号染色体长臂部分缺失。虽然发现了良性多形性腺瘤的典型易位,但组织学检查未显示多形性腺瘤残留。然而,我们推测该恶性肿瘤很可能起源于先前存在的多形性腺瘤。作为恶性转化的一种机制,本文讨论了位于5号染色体长臂上的一个抑癌基因的缺失。

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