Targeting the tetraspanin CD81 reduces cancer invasion and metastasis

被引:37
|
作者
Vences-Catalan, Felipe [1 ]
Rajapaksa, Ranjani [1 ]
Kuo, Chiung-Chi [1 ]
Miller, Caitlyn L. [2 ]
Lee, Anderson [1 ]
Ramani, Vishnu C. [3 ]
Jeffrey, Stefanie S. [3 ]
Levy, Ronald [1 ]
Levy, Shoshana [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Div Oncol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
关键词
immunotherapy; JAM-A; xenograft; ADHESION MOLECULE-A; CELL INVASION; EXPRESSION; PROTEINS; ANTIBODY; SURFACE; TAPA-1; GROWTH;
D O I
10.1073/pnas.2018961118
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tetraspanins are an evolutionary conserved family of proteins involved in multiple aspects of cell physiology, including proliferation, migration and invasion, protein trafficking, and signal transduction; yet their detailed mechanism of action is unknown. Tetraspanins have no known natural ligands, but their engagement by antibodies has begun to reveal their role in cell biology. Studies of tetraspanin knockout mice and of germline mutations in humans have highlighted their role under normal and pathological conditions. Previously, we have shown that mice deficient in the tetraspanin CD81 developed fewer breast cancer metastases compared to their wild type (WT) counterparts. Here, we show that a unique anti-human CD81 antibody (5A6) effectively halts invasion of triple-negative breast cancer (TNBC) cell lines. We demonstrate that 5A6 induces CD81 clustering at the cell membrane and we implicate JAM-A protein in the ability of this antibody to inhibit tumor cell invasion and migration. Furthermore, in a series of in vivo studies we demonstrate that this antibody inhibits metastases in xenograft models, as well as in syngeneic mice bearing a mouse tumor into which we knocked in the human CD81 epitope recognized by the 5A6 antibody.
引用
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页数:8
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