Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma.
Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma.
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DOI:
10.1016/j.ccell.2017.01.001
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发表时间:
2017-02-13
期刊:
影响因子:
50.3
通讯作者:
Wilkerson MD
中科院分区:
文献类型:
--
作者:
Fishbein L;Leshchiner I;Walter V;Danilova L;Robertson AG;Johnson AR;Lichtenberg TM;Murray BA;Ghayee HK;Else T;Ling S;Jefferys SR;de Cubas AA;Wenz B;Korpershoek E;Amelio AL;Makowski L;Rathmell WK;Gimenez-Roqueplo AP;Giordano TJ;Asa SL;Tischler AS;Cancer Genome Atlas Research Network;Pacak K;Nathanson KL;Wilkerson MD
We report a comprehensive molecular characterization of pheochromocytomas and paragangliomas (PCC/PGLs), a rare tumor type. Multi-platform integration revealed that PCC/PGLs are driven by diverse alterations affecting multiple genes and pathways. Pathogenic germline mutations occurred in eight PCC/PGL susceptibility genes. We identified CSDE1 as a somatically-mutated driver gene, complementing four known drivers (HRAS, RET, EPAS1, NF1). We also discovered fusion genes in PCC/PGL, involving MAML3, BRAF, NGFR and NF1. Integrated analysis classified PCC/PGLs into four molecularly-defined groups: a kinase signaling subtype, a pseudohypoxia subtype, a Wnt-altered subtype, driven by MAML3 and CSDE1, and a cortical admixture subtype. Correlates of metastatic PCC/PGL included the MAML3 fusion gene. This integrated molecular characterization provides a comprehensive foundation for developing PCC/PGL precision medicine.
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影响因子:
8.4
作者:
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通讯作者:
Pacak, Karel
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通讯作者:
Gimenez-Roqueplo, Anne-Paule
DOI:
10.1073/pnas.1319176111
发表时间:
2014-08-12
影响因子:
11.1
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5.7
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DOI:
10.1126/science.1257216
发表时间:
2015-01-16
期刊:
Science (New York, N.Y.)
影响因子:
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通讯作者:
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