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染色体缺失发生在睾丸生殖细胞癌5q的特定区域。

Chromosomal deletions occur in restricted regions of 5q in testicular germ cell cancer.

作者信息

Peng H Q, Liu L, Goss P E, Bailey D, Hogg D

机构信息

Department of Medicine, University of Toronto, Ontario, Canada.

出版信息

Oncogene. 1999 May 27;18(21):3277-83. doi: 10.1038/sj.onc.1202662.

Abstract

Since the biologic behavior and molecular genetic changes observed in testicular germ cell cancer differ from those seen in more common epithelial tumors, it is likely that hitherto uncharacterized genes play a role in the development of germ cell tumors. Our previous work on testicular germ cell cancer suggested that chromosome 5q might contain one or more novel tumor suppressor genes that play a role in this malignancy. In this study, we performed a high resolution loss of heterozygosity (LOH) study of testicular cancer using 37 informative markers on chromosome 5. We detected allelic losses in 20/48 (42%) specimens and identified three common sites of loss on chromosome 5q14, 5q21 and 5q34-qter, defined respectively by minimal regions of deletion of < or = 1 cM, 10 cM and approximately 20 (cM). Using an overlapping series of YACs and radiation hybrid mapping, we have constructed a physical map of the 5q14 deletion that should aid in the isolation and characterization of the putative tumor suppressor gene located therein.

摘要

由于睾丸生殖细胞癌中观察到的生物学行为和分子遗传学变化不同于更常见的上皮性肿瘤,因此可能有迄今未被鉴定的基因在生殖细胞肿瘤的发生发展中起作用。我们之前关于睾丸生殖细胞癌的研究表明,5号染色体q臂可能包含一个或多个在这种恶性肿瘤中起作用的新的肿瘤抑制基因。在本研究中,我们使用位于5号染色体上的37个信息性标记,对睾丸癌进行了高分辨率杂合性缺失(LOH)研究。我们在20/48(42%)的标本中检测到等位基因缺失,并在5q14、5q21和5q34 - qter区域确定了三个常见的缺失位点,分别由小于或等于1 cM、10 cM和大约20 cM的最小缺失区域定义。利用一系列重叠的酵母人工染色体(YAC)和辐射杂种图谱,我们构建了5q14缺失区域的物理图谱,这将有助于分离和鉴定位于其中的假定肿瘤抑制基因。

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