The Genomic Landscape of Mucinous Breast Cancer

被引:58
|
作者
Pareja, Fresia
Lee, Ju Youn
Brown, David N.
Piscuoglio, Salvatore
Gularte-Merida, Rodrigo
Selenica, Pier
Paula, Arnaud Da Cruz
Arunachalam, Sasi
Kumar, Rahul
Geyer, Felipe C.
Silveira, Catarina
da Silva, Edaise M.
Li, Anqi
Marchio, Caterina
Ng, Charlotte K. Y.
Mariani, Odette
Fuhrmann, Laetitia
Wen, Hannah Y.
Norton, Larry
Vincent-Salomon, Anne
Brogi, Edi
Reis-Filho, Jorge S.
Weigelt, Britta
机构
[1] Department of Pathology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, 10065, NY
[2] Institute of Pathology, University Hospital Basel, Basel
[3] GenoMed SA, Instituto de Medicina Molecular, Universidade de Lisboa, Lisboa
[4] Department of Medical Sciences, FPO-Canndiolo Cancer Institute, University of Turin, Turin
[5] Départment de Médecine Diagnostique et Théranostique, Institute Curie, Paris
[6] Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY
来源
关键词
CARCINOMA; DIFFERENTIATION; PROGRESSION; TUMORS; PURE;
D O I
10.1093/jnci/djy216
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mucinous carcinoma of the breast (MCB) is a rare histologic form of estrogen receptor (ER)-positive/HER2-negative breast cancer (BC) characterized by tumor cells floating in lakes of mucin. We assessed the genomic landscape of 32 MCBs by whole-exome sequencing and/or RNA-sequencing. GATA3 (23.8%), KMT2C (19.0%), and MAP3K1 (14.3%) were the most frequently mutated genes in pure MCBs. In addition, two recurrent but not pathognomonic fusion genes, OAZ1-CSNK1G2 and RFC4-LPP, were detected in 3/31 (9.7%) and 2/31 (6.5%) samples, respectively. Compared with ER-positive/HER2-negative common forms of BC, MCBs displayed lower PIK3CA and TP53 mutation rates and fewer concurrent 1q gains and 16q losses. Clonal decomposition analysis of the mucinous and ductal components independently microdissected from five mixed MCBs revealed that they are clonally related and evolve following clonal selection or parallel evolution. Our findings indicate that MCB represents a genetically distinct ER-positive/HER2-negative form of BC.
引用
收藏
页码:737 / 741
页数:5
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