Abstract
We report a comprehensive molecular characterization of pheochromocytomas and paragangliomas (PCCs/PGLs), a rare tumor type. Multi-platform integration revealed that PCCs/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, and NF1). We also discovered fusion genes in PCCs/PGLs, involving MAML3, BRAF, NGFR, and NF1. Integrated analysis classified PCCs/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 PCCs/PGLs included the MAML3 fusion gene. This integrated molecular characterization provides a comprehensive foundation for developing PCC/PGL precision medicine.
Original language | English |
---|---|
Pages (from-to) | 181-193 |
Number of pages | 13 |
Journal | Cancer Cell |
Volume | 31 |
Issue number | 2 |
DOIs | |
Publication status | Published - 13 Feb 2017 |
Externally published | Yes |
Keywords
- CSDE1
- MAML3
- TCGA
- expression subtypes
- genomics
- metastasis
- molecular profiling
- paraganglioma
- pheochromocytoma
- sequencing
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In: Cancer Cell, Vol. 31, No. 2, 13.02.2017, p. 181-193.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma
AU - Fishbein, Lauren
AU - Leshchiner, Ignaty
AU - Walter, Vonn
AU - Danilova, Ludmila
AU - Robertson, A. Gordon
AU - Johnson, Amy R.
AU - Lichtenberg, Tara M.
AU - Murray, Bradley A.
AU - Ghayee, Hans K.
AU - Else, Tobias
AU - Ling, Shiyun
AU - Jefferys, Stuart R.
AU - de Cubas, Aguirre A.
AU - Wenz, Brandon
AU - Korpershoek, Esther
AU - Amelio, Antonio L.
AU - Makowski, Liza
AU - Rathmell, W. Kimryn
AU - Gimenez-Roqueplo, Anne Paule
AU - Giordano, Thomas J.
AU - Asa, Sylvia L.
AU - Tischler, Arthur S.
AU - Akbani, Rehan
AU - Ally, Adrian
AU - Amar, Laurence
AU - Arachchi, Harindra
AU - Auchus, Richard J.
AU - Auman, J. Todd
AU - Baertsch, Robert
AU - Balasundaram, Miruna
AU - Balu, Saianand
AU - Bartsch, Detlef K.
AU - Baudin, Eric
AU - Bauer, Thomas
AU - Beaver, Allison
AU - Benz, Christopher
AU - Beroukhim, Rameen
AU - Beuschlein, Felix
AU - Bodenheimer, Tom
AU - Boice, Lori
AU - Bowen, Jay
AU - Bowlby, Reanne
AU - Brooks, Denise
AU - Carlsen, Rebecca
AU - Carter, Suzie
AU - Cassol, Clarissa A.
AU - Cherniack, Andrew D.
AU - Chin, Lynda
AU - Cho, Juok
AU - Chuah, Eric
AU - Chudamani, Sudha
AU - Cope, Leslie
AU - Crain, Daniel
AU - Curley, Erin
AU - de Krijger, Ronald R.
AU - Demchok, John A.
AU - Deutschbein, Timo
AU - Dhalla, Noreen
AU - Dimmock, David
AU - Dinjens, Winand N.M.
AU - Eng, Charis
AU - Eschbacher, Jennifer
AU - Fassnacht, Martin
AU - Felau, Ina
AU - Feldman, Michael
AU - Ferguson, Martin L.
AU - Fiddes, Ian
AU - Frazer, Scott
AU - Gabriel, Stacey B.
AU - Gardner, Johanna
AU - Gastier-Foster, Julie M.
AU - Gehlenborg, Nils
AU - Gerken, Mark
AU - Getz, Gad
AU - Geurts, Jennifer
AU - Goldman, Mary
AU - Graim, Kiley
AU - Gupta, Manaswi
AU - Haan, David
AU - Hahner, Stefanie
AU - Hantel, Constanze
AU - Haussler, David
AU - Hayes, D. Neil
AU - Heiman, David I.
AU - Hoadley, Katherine A.
AU - Holt, Robert A.
AU - Hoyle, Alan P.
AU - Huang, Mei
AU - Hunt, Bryan
AU - Hutter, Carolyn M.
AU - Jones, Steven J.M.
AU - Jones, Corbin D.
AU - Kasaian, Katayoon
AU - Kebebew, Electron
AU - Kim, Jaegil
AU - Kimes, Patrick
AU - Knijnenburg, Theo
AU - Lander, Eric
AU - Lawrence, Michael S.
AU - Lechan, Ronald
AU - Lee, Darlene
AU - Leraas, Kristen M.
AU - Lerario, Antonio
AU - Lin, Pei
AU - Liu, Jia
AU - LiVolsi, Virginia A.
AU - Lolla, Laxmi
AU - Lotan, Yair
AU - Lu, Yiling
AU - Ma, Yussanne
AU - Maison, Nicole
AU - Mallery, David
AU - Mannelli, Massimo
AU - Marquard, Jessica
AU - Marra, Marco A.
AU - Matthew, Thomas
AU - Mayo, Michael
AU - Méatchi, Tchao
AU - Meng, Shaowu
AU - Merino, Maria J.
AU - Mete, Ozgur
AU - Meyerson, Matthew
AU - Mieczkowski, Piotr A.
AU - Mills, Gordon B.
AU - Moore, Richard A.
AU - Morozova, Olena
AU - Morris, Scott
AU - Mose, Lisle E.
AU - Mungall, Andrew J.
AU - Naresh, Rashi
AU - Nathanson, Katherine L.
AU - Newton, Yulia
AU - Ng, Sam
AU - Ni, Ying
AU - Noble, Michael S.
AU - Nwariaku, Fiemu
AU - Pacak, Karel
AU - Parker, Joel S.
AU - Paul, Evan
AU - Penny, Robert
AU - Perou, Charles M.
AU - Perou, Amy H.
AU - Pihl, Todd
AU - Powers, James
AU - Rabaglia, Jennifer
AU - Radenbaugh, Amie
AU - Ramirez, Nilsa C.
AU - Rao, Arjun
AU - Riester, Anna
AU - Roach, Jeffrey
AU - Sadeghi, Sara
AU - Saksena, Gordon
AU - Salama, Sofie
AU - Saller, Charles
AU - Sandusky, George
AU - Sbiera, Silviu
AU - Schein, Jacqueline E.
AU - Schumacher, Steven E.
AU - Shelton, Candace
AU - Shelton, Troy
AU - Sheth, Margi
AU - Shi, Yan
AU - Shih, Juliann
AU - Shmulevich, Ilya
AU - Simons, Janae V.
AU - Sipahimalani, Payal
AU - Skelly, Tara
AU - Sofia, Heidi J.
AU - Sokolov, Artem
AU - Soloway, Matthew G.
AU - Sougnez, Carrie
AU - Stuart, Josh
AU - Sun, Charlie
AU - Swatloski, Teresa
AU - Tam, Angela
AU - Tan, Donghui
AU - Tarnuzzer, Roy
AU - Tarvin, Katherine
AU - Thiessen, Nina
AU - Thorne, Leigh B.
AU - Timmers, Henri J.
AU - Tse, Kane
AU - Uzunangelov, Vlado
AU - van Berkel, Anouk
AU - Veluvolu, Umadevi
AU - Vicha, Ales
AU - Voet, Doug
AU - Waldmann, Jens
AU - Wan, Yunhu
AU - Wang, Zhining
AU - Wang, Tracy S.
AU - Weaver, Joellen
AU - Weinstein, John N.
AU - Weismann, Dirk
AU - Wilkerson, Matthew D.
AU - Wise, Lisa
AU - Wong, Tina
AU - Wong, Christopher
AU - Wu, Ye
AU - Yang, Liming
AU - Zelinka, Tomas
AU - Zenklusen, Jean C.
AU - Zhang, Jiashan (Julia)
AU - Zhang, Wei
AU - Zhu, Jingchun
AU - Zinzindohoué, Franck
AU - Zmuda, Erik
N1 - Publisher Copyright: © 2017 Elsevier Inc.
PY - 2017/2/13
Y1 - 2017/2/13
N2 - We report a comprehensive molecular characterization of pheochromocytomas and paragangliomas (PCCs/PGLs), a rare tumor type. Multi-platform integration revealed that PCCs/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, and NF1). We also discovered fusion genes in PCCs/PGLs, involving MAML3, BRAF, NGFR, and NF1. Integrated analysis classified PCCs/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 PCCs/PGLs included the MAML3 fusion gene. This integrated molecular characterization provides a comprehensive foundation for developing PCC/PGL precision medicine.
AB - We report a comprehensive molecular characterization of pheochromocytomas and paragangliomas (PCCs/PGLs), a rare tumor type. Multi-platform integration revealed that PCCs/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, and NF1). We also discovered fusion genes in PCCs/PGLs, involving MAML3, BRAF, NGFR, and NF1. Integrated analysis classified PCCs/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 PCCs/PGLs included the MAML3 fusion gene. This integrated molecular characterization provides a comprehensive foundation for developing PCC/PGL precision medicine.
KW - CSDE1
KW - MAML3
KW - TCGA
KW - expression subtypes
KW - genomics
KW - metastasis
KW - molecular profiling
KW - paraganglioma
KW - pheochromocytoma
KW - sequencing
UR - http://www.scopus.com/inward/record.url?scp=85011305911&partnerID=8YFLogxK
U2 - 10.1016/j.ccell.2017.01.001
DO - 10.1016/j.ccell.2017.01.001
M3 - Article
C2 - 28162975
AN - SCOPUS:85011305911
SN - 1535-6108
VL - 31
SP - 181
EP - 193
JO - Cancer Cell
JF - Cancer Cell
IS - 2
ER -