CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding

被引:43
作者
Adam, P. J.
Terrett, J. A.
Steers, G.
Stockwin, L.
Loader, J. A.
Fletcher, G. C.
Lu, L-S
Leach, B. I.
Mason, S.
Stamps, A. C.
Boyd, R. S.
Pezzella, F.
Gatter, K. C.
Harris, A. L.
机构
[1] Celltech Ltd, Antibody Ctr Excellence, Slough SL1 4EN, Berks, England
[2] Medarex Inc, Milpitas, CA 94022 USA
[3] John Radcliffe Hosp, Weatherall Inst Mol Med, Canc Res UK, Mol Oncol Labs, Oxford OX3 9DS, England
[4] Univ Leicester, MRC, Toxicol Unit, Leicester, Leics, England
关键词
proteomics; renal cell carcinoma (RCC); CD70; antibody; internalisation;
D O I
10.1038/sj.bjc.6603222
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In order to identify potential markers of renal cancer, the plasma membrane protein content of renal cell carcinoma (RCC)-derived cell lines was annotated using a proteomics process. One unusual protein identified at high levels in A498 and 786-O cells was CD70 (TNFSF7), a type II transmembrane receptor normally expressed on a subset of B, T and NK cells, where it plays a costimulatory role in immune cell activation. Immunohistochemical analysis of CD70 expression in multiple carcinoma types demonstrated strong CD70 staining in RCC tissues. Metastatic tissues from eight of 11 patients with clear cell RCC were positive for CD70 expression. Immunocytochemical analysis demonstrated that binding of an anti-CD70 antibody to CD70 endogenously expressed on the surface of A498 and 786-O cell lines resulted in the rapid internalisation of the antibody-receptor complex. Coincubation of the internalising anti-CD70 antibody with a saporin-conjugated secondary antibody before addition to A498 cells resulted in 50% cell killing. These data indicate that CD70 represents a potential target antigen for toxin-conjugated therapeutic antibody treatment of RCC.
引用
收藏
页码:298 / 306
页数:9
相关论文
共 45 条
[1]   Comprehensive proteomic analysis of breast cancer cell membranes reveals unique proteins with potential roles in clinical cancer [J].
Adam, PJ ;
Boyd, R ;
Tyson, KL ;
Fletcher, GC ;
Stamps, A ;
Hudson, L ;
Poyser, HR ;
Redpath, N ;
Griffiths, M ;
Steers, G ;
Harris, AL ;
Patel, S ;
Berry, J ;
Loader, JA ;
Townsend, RR ;
Daviet, L ;
Legrain, P ;
Parekh, R ;
Terrett, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6482-6489
[2]  
AGATHANGGELOU A, 1995, AM J PATHOL, V147, P1152
[3]   CD27/CD70 INTERACTION DIRECTLY DRIVES B-CELL IGG AND IGM SYNTHESIS [J].
AGEMATSU, K ;
KOBATA, T ;
YANG, FC ;
NAKAZAWA, T ;
FUKUSHIMA, K ;
KITAHARA, M ;
MORI, T ;
SUGITA, K ;
MORIMOTO, C ;
KOMIYAMA, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (10) :2825-2829
[4]   Constitutive CD27/CD70 interaction induces expansion of effector-type T cells and results in IFNγ-mediated B cell depletion [J].
Arens, R ;
Tesselaar, K ;
Baars, PA ;
van Schijndel, GMW ;
Hendriks, J ;
Pals, ST ;
Krimpenfort, P ;
Borst, J ;
van Oers, MHJ ;
van Lier, RAW .
IMMUNITY, 2001, 15 (05) :801-812
[5]   CD27 and CD70 in T cell and B cell activation [J].
Borst, J ;
Hendriks, J ;
Xiao, YL .
CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (03) :275-281
[6]  
BOWMAN MR, 1994, J IMMUNOL, V152, P1756
[7]  
BROWN GR, 1995, J IMMUNOL, V154, P3686
[8]  
Bui MHT, 2003, CLIN CANCER RES, V9, P802
[9]   Induction of T-cell antitumor immunity and protection against tumor growth by secretion of soluble human CD70 molecules [J].
Cormary, C ;
Gonzalez, R ;
Faye, JC ;
Favre, G ;
Tilkin-Mariamé, AF .
CANCER GENE THERAPY, 2004, 11 (07) :497-507
[10]  
Divgi CR, 1998, CLIN CANCER RES, V4, P2729