Programmed Cell Death Ligand 1 Expression in Canine Cancer

被引:2
|
作者
Shosu, Kazuha [1 ]
Sakurai, Masashi [2 ]
Inoue, Kumi [1 ]
Nakagawa, Takayuki [4 ]
Sakai, Hiroki [5 ]
Morimoto, Masahiro [2 ]
Okuda, Masaru [3 ,6 ]
Noguchi, Shunsuke [1 ,6 ]
Mizuno, Takuya [1 ,6 ]
机构
[1] Yamaguchi Univ, Joint Fac Vet Med, Lab Mol Diagnost & Therapeut, 1677-1 Yoshida, Yamaguchi 7538515, Japan
[2] Yamaguchi Univ, Joint Fac Vet Med, Lab Vet Pathol, Yamaguchi 7538515, Japan
[3] Yamaguchi Univ, Joint Fac Vet Med, Lab Vet Internal Med, Yamaguchi 7538515, Japan
[4] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Vet Surg, Bunkyo Ku, Tokyo 113, Japan
[5] Gifu Univ, Fac Appl Biol Sci, Dept Vet Med, Lab Vet Pathol, Gifu, Japan
[6] Yamaguchi Univ, United Grad Sch Vet Sci, Biomed Sci Ctr Translat Res, Yamaguchi 7538515, Japan
来源
IN VIVO | 2016年 / 30卷 / 03期
关键词
Canine cancer; immunohistochemistry; programmed cell death ligand 1; PD-L1; B7-H1; PD-L1; CLINICAL-SIGNIFICANCE; B7; FAMILY; T-CELLS; TUMOR; CARCINOMA; IMMUNOTHERAPY; OVEREXPRESSION; ACTIVATION; PROGNOSIS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Antibody therapy targeting programmed cell death-1 (PD-1) and programmed cell death-ligand 1 (PD-L1) is a promising therapy in human cancer, but only limited information on PD-L1 expression in canine tumors is available. Materials and Methods: PD-L1 expression was examined in 31 canine tumor cell lines of various origins by flow cytometry and western blotting, and in canine tumor and normal tissue specimens by immunohistochemistry. Results: PD-L1 was only expressed on the cell surface of a small number of cell lines but was found expressed within the cells of almost all cell lines. Immunohistochemistry revealed that PD-L1 is frequently expressed in malignant melanoma, mammary gland tumor, mast cell tumor and lymphoma, but less frequently in softtissue sarcoma and hemangiosarcoma. PD-L1 was also expressed in some of the cells of normal canine tissue specimens. Conclusion: Canine tumors with PD-L1 expression that were identified in this study are potential candidates for antiPD-1 and antiPD-L1 therapy.
引用
收藏
页码:195 / 204
页数:10
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