Improving TNF as a cancer therapeutic: Tailor-made TNF fusion proteins with conserved antitumor activity and reduced systemic side effects

被引:20
作者
Gerspach, Jeannette [1 ]
Pfizenmaier, Klaus [1 ]
Wajant, Harald [2 ]
机构
[1] Univ Stuttgart, Inst Cell Biol & Immunol, Stuttgart, Germany
[2] Univ Wurzburg, Dept Mol Internal Med, Med Clin & Polyclin 2, Wurzburg, Germany
基金
芬兰科学院;
关键词
TNF fusion protein; TNF prodrug; TUMOR-NECROSIS-FACTOR; T-CELL-ACTIVATION; FACTOR-ALPHA; FACTOR-RECEPTOR; TARGETED DELIVERY; IN-VIVO; MATRIX METALLOPROTEINASES; RESTRICTED ACTIVATION; HUMAN-MELANOMA; TISSUE FACTOR;
D O I
10.1002/biof.50
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor necrosis factor (TNF) is highly pleiotropic cytokine regulating diverse cellular processes such as proliferation, cell migration, angiogenesis, differentiation, apoptosis, necrosis, but also survival. Because of its name-giving tumor necrosis-inducing capabilities, TNF has attracted attention very early for antitumor therapy. Although TNF is in clinical use for treatment of soft tissue sarcoma in isolated limb perfusion, its broad use in tumor therapy is prevented so far by its strong systemic proinflammatory effects. Nevertheless, over the past decade, a variety of tailor-made TNF variants have been developed with the aim to reduce TNFs systemic activity without losing its antitumoral effects. Here, we review the progress made toward improving the efficacy of TNF by genetic engineering, tumor targeting, and introduction of prodrug concepts.
引用
收藏
页码:364 / 372
页数:9
相关论文
共 77 条
[1]   Identification of tumor necrosis factor (TNF) amino acids crucial for binding to the murine p75 TNF receptor and construction of receptor-selective mutants [J].
Ameloot, P ;
Fiers, W ;
De Bleser, P ;
Ware, CF ;
Vandenabeele, P ;
Brouckaert, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (40) :37426-37430
[2]  
[Anonymous], REGISTRY FEDERALLY P
[3]   Regulation of TCR-mediated T cell activation by TNF-RII [J].
Aspalter, RM ;
Eibl, MM ;
Wolf, HM .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 74 (04) :572-582
[4]   Defective T-cell activation caused by impairment of the TNF receptor 2 costimulatory pathway in common variable immunodeficiency [J].
Aspalter, Rosa M. ;
Eibl, Martha M. ;
Wolf, Hermann M. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2007, 120 (05) :1193-1200
[5]   Evolving role of uPA/uPAR system in human cancers [J].
Ass, Kathleen ;
Ahmad, Aamir ;
Azmi, Asfar S. ;
Sarkar, Sarah H. ;
Sarkar, Fazlul H. .
CANCER TREATMENT REVIEWS, 2008, 34 (02) :122-136
[6]   A CD40-CD95L fusion protein interferes with CD40L-induced prosurvival signaling and allows membrane CD40L-restricted activation of CD95 [J].
Assohou-Luty, Constance ;
Gerspach, Jeanette ;
Siegmund, Daniela ;
Mueller, Nicole ;
Huard, Bertrand ;
Tiegs, Gisa ;
Pfizenmaier, Klaus ;
Wajant, Harald .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2006, 84 (09) :785-797
[7]   TNF-α in promotion and progression of cancer [J].
Balkwill, Frances .
CANCER AND METASTASIS REVIEWS, 2006, 25 (03) :409-416
[8]   Targeted delivery of tumor necrosis factor-α to tumor vessels induces a therapeutic T cell-mediated immune response that protects the host against syngeneic tumors of different histologic origin [J].
Balza, E ;
Mortara, L ;
Sassi, F ;
Monteghirfo, S ;
Carnemolla, B ;
Castellani, P ;
Neri, D ;
Accolla, RS ;
Zardi, L ;
Borsi, L .
CLINICAL CANCER RESEARCH, 2006, 12 (08) :2575-2582
[9]   Targeted bioactivity of membrane-anchored TNF by an antibody-derived TNF fusion protein [J].
Bauer, S ;
Adrian, N ;
Williamson, B ;
Panousis, C ;
Fadle, N ;
Smerd, J ;
Fettah, I ;
Scott, AM ;
Pfreundschuh, M ;
Renner, C .
JOURNAL OF IMMUNOLOGY, 2004, 172 (06) :3930-3939
[10]   Structure-activity profiles of ab-derived TNF fusion proteins [J].
Bauer, Stefan ;
Adrian, Nicole ;
Fischer, Eliane ;
Kleber, Sascha ;
Stenner, Frank ;
Wadle, Andreas ;
Fadle, Natalie ;
Zoellner, Andy ;
Bernhardt, Rita ;
Knuth, Alexander ;
Old, Lloyd J. ;
Renner, Christoph .
JOURNAL OF IMMUNOLOGY, 2006, 177 (04) :2423-2430