• 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

癌症基因组图谱:乳腺癌的临床应用。

The Cancer Genome Atlas: clinical applications for breast cancer.

出版信息

Oncology (Williston Park). 2013 Dec;27(12):1263-9, 1274-9.

PMID:24624545
Abstract

Advances in next-generation sequencing technologies in recent years have allowed in-depth study of somatic mutations in over 1,000 breast cancer samples.The Cancer Genome Atlas (TCGA) is the largest single genome-characterization effort to date. It is remarkable for the integration of DNA sequencing with genome-wide profiling of the epigenome, microRNAome, transcriptome, and proteome for more than 500 diverse primary untreated breast cancers. This article aims to provide an overview ofTCGA findings, with a particular focus on their potential biological relevance and therapeutic implications.

摘要

近年来,下一代测序技术的进步使得对超过 1000 个乳腺癌样本中的体细胞突变进行深入研究成为可能。癌症基因组图谱(TCGA)是迄今为止最大的单一基因组特征分析工作。它的显著特点是将 DNA 测序与对超过 500 个不同的未经治疗的原发性乳腺癌的全基因组表观基因组、microRNAome、转录组和蛋白质组进行整合。本文旨在概述 TCGA 的发现,特别关注其潜在的生物学相关性和治疗意义。

相似文献

1
The Cancer Genome Atlas: clinical applications for breast cancer.癌症基因组图谱:乳腺癌的临床应用。
Oncology (Williston Park). 2013 Dec;27(12):1263-9, 1274-9.
2
Research and clinical applications of cancer genome sequencing.癌症基因组测序的研究与临床应用。
Curr Opin Obstet Gynecol. 2013 Feb;25(1):3-10. doi: 10.1097/GCO.0b013e32835af17c.
3
Initial experience with genomic profiling of heavily pretreated breast cancers.对经过大量预处理的乳腺癌进行基因组分析的初步经验。
Ann Surg Oncol. 2014 Oct;21(10):3216-22. doi: 10.1245/s10434-014-3925-x. Epub 2014 Jul 22.
4
Comprehensive genomic sequencing and the molecular profiles of clinically advanced breast cancer.临床晚期乳腺癌的综合基因组测序与分子图谱
Pathology. 2017 Feb;49(2):120-132. doi: 10.1016/j.pathol.2016.11.005. Epub 2016 Dec 26.
5
Detection of mitochondrial DNA mutations by high-throughput sequencing in the blood of breast cancer patients.高通量测序检测乳腺癌患者血液中的线粒体 DNA 突变。
Int J Mol Med. 2014 Jan;33(1):77-82. doi: 10.3892/ijmm.2013.1559. Epub 2013 Nov 19.
6
Use of linkage analysis, genome-wide association studies, and next-generation sequencing in the identification of disease-causing mutations.在识别致病突变中连锁分析、全基因组关联研究及新一代测序的应用。
Methods Mol Biol. 2013;1015:127-46. doi: 10.1007/978-1-62703-435-7_8.
7
Whole-exome sequencing reveals recurrent somatic mutation networks in cancer.全外显子组测序揭示癌症中反复出现的体细胞突变网络。
Cancer Lett. 2013 Nov 1;340(2):270-6. doi: 10.1016/j.canlet.2012.11.002. Epub 2012 Nov 12.
8
Genetic testing today.当今的基因检测。
Ann Surg Oncol. 2014 Oct;21(10):3209-15. doi: 10.1245/s10434-014-3906-0. Epub 2014 Jul 17.
9
Molecular classification of breast tumors: toward improved diagnostics and treatments.乳腺肿瘤的分子分类:迈向更精准的诊断与治疗
Methods Mol Biol. 2007;360:91-114. doi: 10.1385/1-59745-165-7:91.
10
Next generation analysis of breast cancer genomes for precision medicine.下一代乳腺癌基因组分析用于精准医疗。
Cancer Lett. 2013 Oct 1;339(1):1-7. doi: 10.1016/j.canlet.2013.07.018. Epub 2013 Jul 20.

引用本文的文献

1
Efficacy and safety of first-line CDK4/6 inhibitors plus AI therapy for patients with HR +/HER2- advanced breast cancer: a network meta-analysis.一线CDK4/6抑制剂联合芳香化酶抑制剂治疗HR +/HER2-晚期乳腺癌患者的疗效和安全性:一项网状Meta分析。
BMC Cancer. 2025 May 8;25(1):843. doi: 10.1186/s12885-025-14194-w.
2
Identification and multi-dimensional validation of mitochondrial permeability transition-driven necrosis-related model to assess the prognosis and immunotherapy value in breast cancer.线粒体通透性转换驱动的坏死相关模型的鉴定与多维度验证,以评估乳腺癌的预后和免疫治疗价值
Eur J Med Res. 2025 Feb 18;30(1):113. doi: 10.1186/s40001-025-02370-4.
3
Promoter hypomethylation and overexpression of TSTD1 mediate poor treatment response in breast cancer.
TSTD1的启动子低甲基化和过表达介导乳腺癌治疗反应不佳。
Front Oncol. 2022 Nov 7;12:1004261. doi: 10.3389/fonc.2022.1004261. eCollection 2022.
4
miR-139-5p Was Identified as Biomarker of Different Molecular Subtypes of Breast Carcinoma.miR-139-5p被鉴定为乳腺癌不同分子亚型的生物标志物。
Front Oncol. 2022 Mar 31;12:857714. doi: 10.3389/fonc.2022.857714. eCollection 2022.
5
Triple Negative Breast Cancer in an Appalachian Region: Exponential Tumor Grade Increase with Age of Diagnosis.阿巴拉契亚地区的三阴性乳腺癌:肿瘤分级随诊断年龄呈指数增长。
J Appalach Health. 2021;3(3):97-109. doi: 10.13023/jah.0303.08.
6
Precision Medicine in Low- and Middle-Income Countries.中低收入国家的精准医学。
Annu Rev Pathol. 2022 Jan 24;17:387-402. doi: 10.1146/annurev-pathol-042320-034052.
7
The roles and mechanisms of the circular RNA circ_104640 in early-stage lung adenocarcinoma: a potential diagnostic and therapeutic target.环状RNA circ_104640在早期肺腺癌中的作用及机制:一个潜在的诊断和治疗靶点
Ann Transl Med. 2021 Jan;9(2):138. doi: 10.21037/atm-20-8019.
8
Key Genes and Prognostic Analysis in HER2+ Breast Cancer.HER2+ 乳腺癌的关键基因与预后分析。
Technol Cancer Res Treat. 2021 Jan-Dec;20:1533033820983298. doi: 10.1177/1533033820983298.
9
Distinct pattern of one-carbon metabolism, a nutrient-sensitive pathway, in invasive breast cancer: A metabolomic study.浸润性乳腺癌中一碳代谢(一种营养敏感途径)的独特模式:一项代谢组学研究。
Oncotarget. 2020 May 5;11(18):1637-1652. doi: 10.18632/oncotarget.27575.
10
Doubling-Times and Halving-Times May Predict CML Response to Tyrosine Kinase Inhibitors.倍增时间和减半时间可能预测慢性粒细胞白血病对酪氨酸激酶抑制剂的反应。
Front Oncol. 2019 Aug 13;9:764. doi: 10.3389/fonc.2019.00764. eCollection 2019.