Mesothelin, a novel immunotherapy target for triple negative breast cancer

被引:121
|
作者
Tchou, Julia [1 ,2 ,3 ,4 ]
Wang, Liang-Chuan [5 ]
Selven, Ben [2 ,3 ]
Zhang, Hongtao [6 ]
Conejo-Garcia, Jose [7 ]
Borghaei, Hossein [8 ]
Kalos, Michael [4 ,6 ,9 ]
Vondeheide, Robert H. [4 ,9 ]
Albelda, Steven M. [5 ]
June, Carl H. [4 ,6 ,9 ]
Zhang, Paul J. [6 ]
机构
[1] Perelman Ctr Adv Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Surg, Div Endocrine & Oncol Surg, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Rena Rowan Breast Ctr, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Thorac Oncol Res Lab, Div Pulm, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[7] Wistar Inst Anat & Biol, Tumor Microenvironm & Metastasis Program, Philadelphia, PA 19104 USA
[8] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[9] Univ Penn, Perelman Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
关键词
Mesothelin; Breast cancer subtypes; Triple negative breast cancer; Chimeric antigen receptor; Immunotherapy; HUMAN T-CELLS; MONOCLONAL-ANTIBODY; TUMOR; EXPRESSION; RECEPTOR; CARCINOMAS; SUBTYPES; BASAL; K1;
D O I
10.1007/s10549-012-2018-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mesothelin is a cell-surface glycoprotein present on mesothelial cells and elicits T cell responses in a variety of cancers including pancreatic, biliary and ovarian cancer. Breast cancer is not known to express mesothelin. We postulated that mesothelin may be a unique tumor-associated antigen in triple negative breast cancer (TNBC), a less common breast cancer subtype which may have been under-represented in prior studies that characterized mesothelin expression. Therefore, we screened 99 primary breast cancer samples by immunohistochemistry analysis using formalin-fixed paraffin-embedded archival tumor tissues and confirmed that mesothelin was overexpressed in the majority of TNBC (67 %) but only rarely in < 5 % ER(+) or Her2-neu(+) breast cancer, respectively. To determine whether mesothelin may be exploited as a novel immunotherapy target in breast cancer, an in vitro cell killing assay was performed to compare the ability of genetically modified T cells expressing a chimeric antibody receptor (CAR) specific for mesothelin (mesoCAR T cells) or non-transduced T cells to kill mesothelin-expressing primary breast cancer cells. A significantly higher anti-tumor cytotoxicity by mesoCAR T cells was observed (31.7 vs. 8.7 %, p < 0.001). Our results suggest that mesothelin has promise as a novel immunotherapy target for TNBC for which effective targeted therapy is lacking to date.
引用
收藏
页码:799 / 804
页数:6
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