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与人类乳腺癌进展相关的一个肿瘤抑制基因定位在8号染色体短臂22区至23.1区1厘摩的区间内。

Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1.

作者信息

Yokota T, Yoshimoto M, Akiyama F, Sakamoto G, Kasumi F, Nakamura Y, Emi M

机构信息

Department of Molecular Biology, Institute of Gerontology, Nippon Medical School, Kawasaki, Japan.

出版信息

Cancer. 1999 Jan 15;85(2):447-52.

Abstract

BACKGROUND

Frequent allelic losses on the short arm of chromosome 8 in several types of human cancers, and deletion maps of this region in tumor DNAs, have suggested that 8p harbors one or more genes that are important for suppressing tumorigenesis in the tissues in question.

METHODS

To define the locations of potential tumor suppressor genes involved in breast carcinoma, the authors examined 144 primary breast carcinomas for loss of heterozygosity at 18 highly polymorphic microsatellite loci on 8p. They also sought correlations between allelic loss on 8p and several clinicopathologic parameters.

RESULTS

Allelic loss was observed in 74 of the 144 sporadic breast carcinomas examined. Whereas more than half of the informative tumors showed loss of an allele at every locus on the short arm, 32 showed partial or interstitial deletions. Deletion mapping in this panel of tumors identified two distinct commonly deleted regions, one in a 1-cM interval flanked by D8S511 and D8S1991 at 8p22-p23.1, and the other in a 16-cM interval flanked by D8S136 and D8S1477 at 8p22-p21. Allelic losses in both of these regions were observed more frequently in tumors of the solid-tubular or scirrhous type than in less aggressive histologic types. Furthermore, allelic loss in either region occurred more frequently in larger and infiltrative tumors (T1 < T2 < T3).

CONCLUSIONS

The association of allelic losses on 8p with advanced tumor stage and aggressive histologic type implies that loss or inactivation of one of at least two putative tumor suppressor genes on 8p may contribute to the progression of breast carcinoma.

摘要

背景

在几种人类癌症中,8号染色体短臂上频繁出现等位基因缺失,并且肿瘤DNA中该区域的缺失图谱表明,8p含有一个或多个对抑制相关组织肿瘤发生很重要的基因。

方法

为了确定与乳腺癌相关的潜在抑癌基因的位置,作者检测了144例原发性乳腺癌在8p上18个高度多态性微卫星位点的杂合性缺失情况。他们还探寻了8p上等位基因缺失与几个临床病理参数之间的相关性。

结果

在所检测的144例散发性乳腺癌中,有74例观察到等位基因缺失。虽然超过一半的信息性肿瘤在短臂上的每个位点都显示一个等位基因缺失,但有32例显示部分或间质缺失。在这组肿瘤中进行的缺失图谱分析确定了两个不同的常见缺失区域,一个在8p22 - p23.1处,由D8S511和D8S1991侧翼的1 cM区间内;另一个在8p22 - p​​21处,由D8S136和D8S1477侧翼的16 cM区间内。与侵袭性较小的组织学类型相比,在实体管状或硬癌类型的肿瘤中更频繁地观察到这两个区域的等位基因缺失。此外,在较大的浸润性肿瘤(T1 < T2 < T3)中,任一区域的等位基因缺失更频繁地发生。

结论

8p上等位基因缺失与肿瘤晚期和侵袭性组织学类型的关联意味着,8p上至少两个推定的抑癌基因之一的缺失或失活可能促进乳腺癌的进展。

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