Oncogenic Signaling Pathways in The Cancer Genome Atlas.

Oncogenic Signaling Pathways in The Cancer Genome Atlas.
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癌症基因组地图集中的致癌信号通路。

DOI:
10.1016/j.cell.2018.03.035
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发表时间:
2018-04-05
期刊:
影响因子:
64.5
通讯作者:
Schultz N
Schultz N
中科院分区:
生物学1区
文献类型:
--
作者:
Sanchez-Vega F;Mina M;Armenia J;Chatila WK;Luna A;La KC;Dimitriadoy S;Liu DL;Kantheti HS;Saghafinia S;Chakravarty D;Daian F;Gao Q;Bailey MH;Liang WW;Foltz SM;Shmulevich I;Ding L;Heins Z;Ochoa A;Gross B;Gao J;Zhang H;Kundra R;Kandoth C;Bahceci I;Dervishi L;Dogrusoz U;Zhou W;Shen H;Laird PW;Way GP;Greene CS;Liang H;Xiao Y;Wang C;Iavarone A;Berger AH;Bivona TG;Lazar AJ;Hammer GD;Giordano T;Kwong LN;McArthur G;Huang C;Tward AD;Frederick MJ;McCormick F;Meyerson M;Cancer Genome Atlas Research Network;Van Allen EM;Cherniack AD;Ciriello G;Sander C;Schultz N

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控制细胞周期进程、细胞凋亡和细胞生长的信号通路中的遗传改变是癌症的常见标志,但这些通路中的改变的程度、机制和共同发生在个体肿瘤和肿瘤类型之间不同。使用癌症基因组图谱(TCGA)分析的9,125个肿瘤中的突变,拷贝数变化,mRNA表达,基因融合和DNA甲基化,我们分析了10个经典途径中的体细胞改变的机制和模式:细胞周期,Hippo,Myc,Notch,NRF 2,PI-3-激酶/Akt,RTK-RAS,TGFβ信号传导,P53和β-catenin/WNT。我们绘制了33种癌症类型中通路改变的详细景观,分为64种亚型,并确定了共同发生和相互排斥的模式。89%的肿瘤在这些通路中至少有一个驱动改变,57%的肿瘤至少有一个可能被现有药物靶向的改变。30%的肿瘤有多个靶向改变,这表明联合治疗的机会。通过TCGA分析的> 9,000个肿瘤中10个信号传导通路的遗传改变的综合分析突出了这些通路中单独和共同发生的可操作改变的显著代表性,表明靶向和联合治疗的机会。
Genetic alterations in signaling pathways that control cell cycle progression, apoptosis, and cell growth are common hallmarks of cancer, but the extent, mechanisms, and co-occurrence of alterations in these pathways differ between individual tumors and tumor types. Using mutations, copy-number changes, mRNA expression, gene fusions and DNA methylation in 9,125 tumors profiled by The Cancer Genome Atlas (TCGA), we analyzed the mechanisms and patterns of somatic alterations in 10 canonical pathways: cell cycle, Hippo, Myc, Notch, NRF2, PI-3-Kinase/Akt, RTK-RAS, TGFβ signaling, P53 and β-catenin/WNT. We charted the detailed landscape of pathway alterations in 33 cancer types, stratified into 64 subtypes, and identified patterns of co-occurrence and mutual exclusivity. Eighty-nine percent of tumors had at least one driver alteration in these pathways, and 57% percent of tumors had at least one alteration potentially targetable by currently available drugs. Thirty percent of tumors had multiple targetable alterations, indicating opportunities for combination therapy. An integrated analysis of genetic alterations in 10 signaling pathways in >9,000 tumors profiled by TCGA highlights significant representation of individual and co-occurring actionable alterations in these pathways, suggesting opportunities for targeted and combination therapies.
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作者:
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