Suppr超能文献

国际癌症基因组计划网络。

International network of cancer genome projects.

出版信息

Nature. 2010 Apr 15;464(7291):993-8. doi: 10.1038/nature08987.

Abstract

The International Cancer Genome Consortium (ICGC) was launched to coordinate large-scale cancer genome studies in tumours from 50 different cancer types and/or subtypes that are of clinical and societal importance across the globe. Systematic studies of more than 25,000 cancer genomes at the genomic, epigenomic and transcriptomic levels will reveal the repertoire of oncogenic mutations, uncover traces of the mutagenic influences, define clinically relevant subtypes for prognosis and therapeutic management, and enable the development of new cancer therapies.

摘要

国际癌症基因组联盟(ICGC)成立的目的是协调全球范围内 50 种不同癌症类型和/或亚型的肿瘤的大规模癌症基因组研究。在基因组、表观基因组和转录组水平上对超过 25000 个癌症基因组进行系统研究,将揭示致癌突变的全部内容,揭示诱变影响的痕迹,为预后和治疗管理定义具有临床意义的亚型,并能够开发新的癌症疗法。

相似文献

1
International network of cancer genome projects.
Nature. 2010 Apr 15;464(7291):993-8. doi: 10.1038/nature08987.
2
Cancer: drivers and passengers.
Nature. 2007 Mar 8;446(7132):145-6. doi: 10.1038/446145a.
3
Genomics sizes up.
Nature. 2008 Jan 17;451(7176):234. doi: 10.1038/451234a.
4
International genome project launched.
Nature. 2008 Jan 24;451(7177):378-9. doi: 10.1038/451378b.
5
Pan-cancer analysis of whole genomes.
Nature. 2020 Feb;578(7793):82-93. doi: 10.1038/s41586-020-1969-6. Epub 2020 Feb 5.
6
Discovery and saturation analysis of cancer genes across 21 tumour types.
Nature. 2014 Jan 23;505(7484):495-501. doi: 10.1038/nature12912. Epub 2014 Jan 5.
7
Big science: The cancer genome challenge.
Nature. 2010 Apr 15;464(7291):972-4. doi: 10.1038/464972a.
8
Patterns of somatic mutation in human cancer genomes.
Nature. 2007 Mar 8;446(7132):153-8. doi: 10.1038/nature05610.
9
The Global Cancer Genomics Consortium: interfacing genomics and cancer medicine.
Cancer Res. 2012 Aug 1;72(15):3720-4. doi: 10.1158/0008-5472.CAN-12-1054. Epub 2012 May 24.

引用本文的文献

1
Hypoxia-induced metastatic heterogeneity in pancreatic cancer.
bioRxiv. 2025 Aug 29:2025.08.26.672389. doi: 10.1101/2025.08.26.672389.
2
A review on multi-omics integration for aiding study design of large scale TCGA cancer datasets.
BMC Genomics. 2025 Aug 22;26(1):769. doi: 10.1186/s12864-025-11925-y.
4
Achieving inclusive healthcare through integrating education and research with AI and personalized curricula.
Commun Med (Lond). 2025 Aug 16;5(1):356. doi: 10.1038/s43856-025-01034-y.
5
Scaling for African Inclusion in High-Throughput Whole Cancer Genome Bioinformatic Workflows.
Cancers (Basel). 2025 Jul 26;17(15):2481. doi: 10.3390/cancers17152481.
7
Methylglyoxal mutagenizes single-stranded DNA via Rev1-associated slippage and mispairing.
Nucleic Acids Res. 2025 Jul 19;53(14). doi: 10.1093/nar/gkaf705.
8
Cancer genomics and bioinformatics in Latin American countries: applications, challenges, and perspectives.
Front Oncol. 2025 Jul 9;15:1584178. doi: 10.3389/fonc.2025.1584178. eCollection 2025.
9
Editorial: Molecular markers for pancreatic cancers: new technologies and applications in the clinical practice.
Front Oncol. 2025 Jul 8;15:1651566. doi: 10.3389/fonc.2025.1651566. eCollection 2025.
10
Current Bioinformatics Tools in Precision Oncology.
MedComm (2020). 2025 Jul 9;6(7):e70243. doi: 10.1002/mco2.70243. eCollection 2025 Jul.

本文引用的文献

1
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes.
Nature. 2010 Jan 21;463(7279):360-3. doi: 10.1038/nature08672. Epub 2010 Jan 6.
2
Complex landscapes of somatic rearrangement in human breast cancer genomes.
Nature. 2009 Dec 24;462(7276):1005-10. doi: 10.1038/nature08645.
3
A small-cell lung cancer genome with complex signatures of tobacco exposure.
Nature. 2010 Jan 14;463(7278):184-90. doi: 10.1038/nature08629. Epub 2009 Dec 16.
4
A comprehensive catalogue of somatic mutations from a human cancer genome.
Nature. 2010 Jan 14;463(7278):191-6. doi: 10.1038/nature08658. Epub 2009 Dec 16.
5
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution.
Nature. 2009 Oct 8;461(7265):809-13. doi: 10.1038/nature08489.
6
Prepublication data sharing.
Nature. 2009 Sep 10;461(7261):168-70. doi: 10.1038/461168a.
7
Recurring mutations found by sequencing an acute myeloid leukemia genome.
N Engl J Med. 2009 Sep 10;361(11):1058-66. doi: 10.1056/NEJMoa0903840. Epub 2009 Aug 5.
8
Mutation of FOXL2 in granulosa-cell tumors of the ovary.
N Engl J Med. 2009 Jun 25;360(26):2719-29. doi: 10.1056/NEJMoa0902542. Epub 2009 Jun 10.
10
BioMart Central Portal--unified access to biological data.
Nucleic Acids Res. 2009 Jul;37(Web Server issue):W23-7. doi: 10.1093/nar/gkp265. Epub 2009 May 6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验