• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Genetics and cancer: application to the breast].

作者信息

Lidereau R, Nogues C

机构信息

Laboratoire d'Oncogénétique, Centre René Huguenin, Saint-Cloud.

出版信息

Arch Anat Cytol Pathol. 1995;43(1-2):5-11.

PMID:7794027
Abstract

Various gene systems are involved in events occurring during transformation of a normal cell into a cancer cell. By order of intervention, genes responsible for an increased individual susceptibility to cancer can be distinguished from actual cancer genes, followed by genes involved at other levels of carcinogenesis. 15 to 20% of patients with breast cancer have a first-degree relative affected by the same cancer, although an inherited predisposition to cancer is only established in 4 to 10% of cases. The genetic heterogeneity of familial forms of breast cancer make it difficult to identify susceptibility genes. At the present time, 3 regions of the genome have been implicated in the predisposition to breast cancer in women: the BRCA1 gene, the BRCA2 gene and the TP53 gene. All predisposition genes are able to transmit susceptibility due to a mutation or inherited microdeletion.

摘要

相似文献

1
[Genetics and cancer: application to the breast].
Arch Anat Cytol Pathol. 1995;43(1-2):5-11.
2
[Somatic genetics of breast cancer].
Bull Cancer. 1997 Jan;84(1):83-96.
3
[Biology of solid cancers: breast cancer as an example. First part: genetic systems implicated in carcinogenesis].[实体癌生物学:以乳腺癌为例。第一部分:与致癌作用相关的遗传系统]
J Gynecol Obstet Biol Reprod (Paris). 1996;25(2):131-41.
4
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals.对来自乳腺癌-卵巢癌家族的BRCA1和BRCA2阴性先证者、早发性乳腺癌病例及对照个体中与BRCA1相互作用的基因ZNF350/ZBRK1和BRIP1/BACH1进行突变分析。
Hum Mutat. 2003 Aug;22(2):121-8. doi: 10.1002/humu.10238.
5
Tumor suppressor genes and their alterations in breast cancer.
Semin Cancer Biol. 1995 Jun;6(3):119-25. doi: 10.1006/scbi.1995.0019.
6
A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer families.捷克遗传性乳腺癌和乳腺-卵巢癌家族中BRCA1和BRCA2突变的高发生率。
Cas Lek Cesk. 2000 Oct 11;139(20):635-7.
7
A region close to Tp53 shows LOH in familial breast cancer.在家族性乳腺癌中,靠近Tp53的一个区域显示出杂合性缺失。
Int J Mol Med. 2002 Apr;9(4):405-9.
8
Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study.基于人群的BRCA1和BRCA2中一组特定蛋白质截短突变的乳腺癌平均年龄特异性累积风险估计。澳大利亚乳腺癌家族研究。
Cancer Epidemiol Biomarkers Prev. 1999 Sep;8(9):741-7.
9
THe genetics of familial breast cancer.
Semin Oncol. 1996 Feb;23(1 Suppl 2):1-5.
10
Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers.利用表达数据和CGEMS全基因组乳腺癌关联研究来鉴定可能改变BRCA1/2突变携带者风险的基因。
Breast Cancer Res Treat. 2008 Nov;112(2):229-36. doi: 10.1007/s10549-007-9848-5. Epub 2007 Dec 20.