Molecular Characterization of Basal-Like and Non-Basal-Like Triple-Negative Breast Cancer

被引:418
作者
Prat, Aleix [1 ,2 ,3 ]
Adamo, Barbara [2 ,3 ]
Cheang, Maggie C. U. [4 ]
Anders, Carey K. [4 ]
Carey, Lisa A. [4 ]
Perou, Charles M. [4 ,5 ,6 ]
机构
[1] Vall dHebron Inst Oncol, Translat Genom Unit, Barcelona, Spain
[2] Vall dHebron Inst Oncol, Breast Canc Unit, Barcelona, Spain
[3] Vall dHebron Inst Oncol, Dept Med Oncol, Barcelona, Spain
[4] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
Breast cancer; Subtype; Gene expression; Triple-negative; basal-like; LOW INTRINSIC SUBTYPE; PREMENOPAUSAL WOMEN; RANDOMIZED-TRIAL; CELL-LINES; CHEMOTHERAPY; CYCLOPHOSPHAMIDE; FLUOROURACIL; METASTASIS; PREDICTOR; PACLITAXEL;
D O I
10.1634/theoncologist.2012-0397
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative (TN) and basal-like (BL) breast cancer definitions have been used interchangeably to identify breast cancers that lack expression of the hormone receptors and overexpression and/or amplification of HER2. However, both classifications show substantial discordance rates when compared to each other. Here, we molecularly characterize TN tumors and BL tumors, comparing and contrasting the results in terms of common patterns and distinct patterns for each. In total, when testing 412 TN and 473 BL tumors, 21.4% and 31.5% were identified as non-BL and non-TN, respectively. TN tumors identified as luminal or HER2-enriched (HER2E) showed undistinguishable overall gene expression profiles when compared versus luminal or HER2E tumors that were not TN. Similar findings were ob-served within BL tumors regardless of their TN status, which suggests that molecular subtype is preserved regardless of individual marker results. Interestingly, most TN tumors identified as HER2E showed low HER2 expression and lacked HER2 amplification, despite the similar overall gene expression profiles to HER2E tumors that were clinically HER2-positive. Lastly, additional genomic classifications were examined within TN and BL cancers, most of which were highly concordant with tumor intrinsic subtype. These results suggest that future clinical trials focused on TN disease should consider stratifying patients based upon BL versus non-BL gene expression profiles, which appears to be the main biological difference seen in patients with TN breast cancer. The Oncologist 2013;18:123-133
引用
收藏
页码:123 / 133
页数:11
相关论文
共 59 条
[1]   Breast Carcinomas Arising at a Young Age: Unique Biology or a Surrogate for Aggressive Intrinsic Subtypes? [J].
Anders, Carey K. ;
Fan, Cheng ;
Parker, Joel S. ;
Carey, Lisa A. ;
Blackwell, Kimberly L. ;
Klauber-DeMore, Nancy ;
Perou, Charles M. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (01) :E18-E20
[2]   Generation of tumor-initiating cells by exogenous delivery of OCT4 transcription factor [J].
Beltran, Adriana S. ;
Rivenbark, Ashley G. ;
Richardson, Bryan T. ;
Yuan, Xinni ;
Quian, Haili ;
Hunt, John P. ;
Zimmerman, Eric ;
Graves, Lee M. ;
Blancafort, Pilar .
BREAST CANCER RESEARCH, 2011, 13 (05)
[3]   Genes that mediate breast cancer metastasis to the brain [J].
Bos, Paula D. ;
Zhang, Xiang H. -F. ;
Nadal, Cristina ;
Shu, Weiping ;
Gomis, Roger R. ;
Nguyen, Don X. ;
Minn, Andy J. ;
van de Vijver, Marc J. ;
Gerald, William L. ;
Foekens, John A. ;
Massague, Joan .
NATURE, 2009, 459 (7249) :1005-U137
[4]   Safety and Activity of Anti-PD-L1 Antibody in Patients with Advanced Cancer [J].
Brahmer, Julie R. ;
Tykodi, Scott S. ;
Chow, Laura Q. M. ;
Hwu, Wen-Jen ;
Topalian, Suzanne L. ;
Hwu, Patrick ;
Drake, Charles G. ;
Camacho, Luis H. ;
Kauh, John ;
Odunsi, Kunle ;
Pitot, Henry C. ;
Hamid, Omid ;
Bhatia, Shailender ;
Martins, Renato ;
Eaton, Keith ;
Chen, Shuming ;
Salay, Theresa M. ;
Alaparthy, Suresh ;
Grosso, Joseph F. ;
Korman, Alan J. ;
Parker, Susan M. ;
Agrawal, Shruti ;
Goldberg, Stacie M. ;
Pardoll, Drew M. ;
Gupta, Ashok ;
Wigginton, Jon M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (26) :2455-2465
[5]   A randomized placebo-controlled study of tamoxifen after adjuvant chemotherapy in premenopausal women with early breast cancer (National Cancer Institute of Canada-Clinical Trials Group Trial, MA.12) [J].
Bramwell, V. H. C. ;
Pritchard, K. I. ;
Tu, D. ;
Tonkin, K. ;
Vachhrajani, H. ;
Vandenberg, T. A. ;
Robert, J. ;
Arnold, A. ;
O'Reilly, S. E. ;
Graham, B. ;
Shepherd, L. .
ANNALS OF ONCOLOGY, 2010, 21 (02) :283-290
[6]  
Cameron D, 2012, CANC THER RES CTR AM
[7]  
Cheang M, 2012, P AN M AM SOC CLIN, P1008
[8]   DNA methylation profiling reveals a predominant immune component in breast cancers [J].
Dedeurwaerder, Sarah ;
Desmedt, Christine ;
Calonne, Emilie ;
Singhal, Sandeep K. ;
Haibe-Kains, Benjamin ;
Defrance, Matthieu ;
Michiels, Stefan ;
Volkmar, Michael ;
Deplus, Rachel ;
Luciani, Judith ;
Lallemand, Francoise ;
Larsimont, Denis ;
Toussaint, Jerome ;
Haussy, Sandy ;
Rothe, Francoise ;
Rouas, Ghizlane ;
Metzger, Otto ;
Majjaj, Samira ;
Saini, Kamal ;
Putmans, Pascale ;
Hames, Gerald ;
van Baren, Nicolas ;
Coulie, Pierre G. ;
Piccart, Martine ;
Sotiriou, Christos ;
Fuks, Francois .
EMBO MOLECULAR MEDICINE, 2011, 3 (12) :726-741
[9]   DAVID: Database for annotation, visualization, and integrated discovery [J].
Dennis, G ;
Sherman, BT ;
Hosack, DA ;
Yang, J ;
Gao, W ;
Lane, HC ;
Lempicki, RA .
GENOME BIOLOGY, 2003, 4 (09)
[10]   Genome remodelling in a basal-like breast cancer metastasis and xenograft [J].
Ding, Li ;
Ellis, Matthew J. ;
Li, Shunqiang ;
Larson, David E. ;
Chen, Ken ;
Wallis, Johnw. ;
Harris, Christopher C. ;
McLellan, Michael D. ;
Fulton, Robert S. ;
Fulton, Lucinda L. ;
Abbott, Rachel M. ;
Hoog, Jeremy ;
Dooling, David J. ;
Koboldt, Daniel C. ;
Schmidt, Heather ;
Kalicki, Joelle ;
Zhang, Qunyuan ;
Chen, Lei ;
Lin, Ling ;
Wendl, Michael C. ;
McMichael, Joshua F. ;
Magrini, Vincent J. ;
Cook, Lisa ;
McGrath, Sean D. ;
Vickery, Tammi L. ;
Appelbaum, Elizabeth ;
DeSchryver, Katherine ;
Davies, Sherri ;
Guintoli, Therese ;
Lin, Li ;
Crowder, Robert ;
Tao, Yu ;
Snider, Jacqueline E. ;
Smith, Scott M. ;
Dukes, Adam F. ;
Sanderson, Gabriel E. ;
Pohl, Craig S. ;
Delehaunty, Kim D. ;
Fronick, Catrina C. ;
Pape, Kimberley A. ;
Reed, Jerry S. ;
Robinson, Jody S. ;
Hodges, Jennifer S. ;
Schierding, William ;
Dees, Nathan D. ;
Shen, Dong ;
Locke, Devin P. ;
Wiechert, Madeline E. ;
Eldred, James M. ;
Peck, Josh B. .
NATURE, 2010, 464 (7291) :999-1005