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Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer

生物 浸润性小叶癌 福克斯A1 PTEN公司 癌症研究 乳腺癌 关贸总协定3 癌症 PI3K/AKT/mTOR通路 浸润性导管癌 遗传学 基因 转录因子 信号转导
作者
Giovanni Ciriello,Michael L. Gatza,Andrew H. Beck,Matthew D. Wilkerson,Suhn K. Rhie,Alessandro Pastore,Hailei Zhang,Michael D. McLellan,Christina Yau,Cyriac Kandoth,Reanne Bowlby,Hui Shen,Sikander Hayat,Robert J. Fieldhouse,Susan C. Lester,Gary Tse,Rachel E. Factor,Laura C. Collins,Kimberly H. Allison,Yunn-Yi Chen,Kristin C. Jensen,Nicole B. Johnson,Steffi Oesterreich,Gordon B. Mills,Andrew D. Cherniack,Gordon Robertson,Christopher C. Benz,Chris Sander,Peter W. Laird,Katherine A. Hoadley,Tari A. King,Charles M. Perou,Rehan Akbani,J. Todd Auman,Miruna Balasundaram,Saianand Balu,Thomas Barr,Andrew H. Beck,Christopher C. Benz,Stephen C. Benz,Mario Berríos,Rameen Beroukhim,Tom Bodenheimer,Lori Boice,Moiz S. Bootwalla,Jay Bowen,Reanne Bowlby,Denise Brooks,Andrew D. Cherniack,Lynda Chin,Juok Cho,Sudha Chudamani,Giovanni Ciriello,Tanja M. Davidsen,John A. Demchok,Jennifer B. Dennison,Li Ding,Ina Felau,Martin L. Ferguson,Scott Frazer,Stacey Gabriel,Jianjiong Gao,Julie M. Gastier‐Foster,Michael L. Gatza,Nils Gehlenborg,Mark Gerken,Gad Getz,William J. Gibson,D. Neil Hayes,David I. Heiman,Katherine A. Hoadley,Andrea Holbrook,Robert A. Holt,Alan P. Hoyle,Hai Hu,Mei Huang,Carolyn M. Hutter,E. Shelley Hwang,Stuart R. Jefferys,Steven J. M. Jones,Ju Zhang,Jaegil Kim,Phillip H. Lai,Peter W. Laird,Michael S. Lawrence,Kristen M. Leraas,Tara M. Lichtenberg,Pei Lin,Shiyun Ling,Jia Liu,Wenbin Liu,Laxmi Lolla,Yiling Lu,Yussanne Ma,Dennis T. Maglinte,Elaine R. Mardis,Jeffrey R. Marks,Marco A. Marra,Cynthia McAllister,Michael D. McLellan,Shaowu Meng,Matthew Meyerson,Gordon B. Mills,Richard A. Moore,Lisle E. Mose,Andrew J. Mungall,Bradley A. Murray,Rashi Naresh,Michael S. Noble,Steffi Oesterreich,Olufunmilayo Olopade,Joel S. Parker,Charles M. Perou,Todd Pihl,Gordon Saksena,Steven E. Schumacher,Kenna Shaw,Nilsa C. Ramirez,W. Kimryn Rathmell,Suhn K. Rhie,Jeffrey Roach,A. Gordon Robertson,Gordon Saksena,Chris Sander,Jacqueline E. Schein,Nikolaus Schultz,Hui Shen,Margi Sheth,Yan Shi,Juliann Shih,Carl Simon Shelley,Craig D. Shriver,Janae V. Simons,Heidi J. Sofia,Matthew G. Soloway,Carrie Sougnez,Charlie Sun,Roy Tarnuzzer,Daniel Guimarães Tiezzi,David J. Van Den Berg,Doug Voet,Yunhu Wan,Zhining Wang,John N. Weinstein,Daniel J. Weisenberger,Matthew D. Wilkerson,Richard K. Wilson,Lisa Wise,Maciej Wiznerowicz,Junyuan Wu,Ye Wu,Liming Yang,Christina Yau,Travis I. Zack,Jean C. Zenklusen,Hailei Zhang,Jiashan Zhang,Erik Zmuda
出处
期刊:Cell [Elsevier]
卷期号:163 (2): 506-519 被引量:1475
标识
DOI:10.1016/j.cell.2015.09.033
摘要

Invasive lobular carcinoma (ILC) is the second most prevalent histologic subtype of invasive breast cancer. Here, we comprehensively profiled 817 breast tumors, including 127 ILC, 490 ductal (IDC), and 88 mixed IDC/ILC. Besides E-cadherin loss, the best known ILC genetic hallmark, we identified mutations targeting PTEN, TBX3, and FOXA1 as ILC enriched features. PTEN loss associated with increased AKT phosphorylation, which was highest in ILC among all breast cancer subtypes. Spatially clustered FOXA1 mutations correlated with increased FOXA1 expression and activity. Conversely, GATA3 mutations and high expression characterized luminal A IDC, suggesting differential modulation of ER activity in ILC and IDC. Proliferation and immune-related signatures determined three ILC transcriptional subtypes associated with survival differences. Mixed IDC/ILC cases were molecularly classified as ILC-like and IDC-like revealing no true hybrid features. This multidimensional molecular atlas sheds new light on the genetic bases of ILC and provides potential clinical options.

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