Melanoma-associated Chondroitin Sulfate Proteoglycan (MCSP)-targeted delivery of soluble TRAIL potently inhibits melanoma outgrowth in vitro and in vivo

被引:61
作者
de Bruyn, Marco [1 ]
Rybczynska, Anna A. [2 ]
Wei, Yunwei [1 ,3 ]
Schwenkert, Michael [4 ]
Fey, Georg H. [4 ]
Dierckx, Rudi A. J. O. [2 ]
van Waarde, Aren [2 ]
Helfrich, Wijnand [1 ]
Bremer, Edwin [1 ]
机构
[1] Univ Groningen, Surg Res Labs, Dept Surg, Univ Med Ctr Groningen, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen, Dept Nucl Med & Mol Imaging, Univ Med Ctr Groningen, NL-9713 GZ Groningen, Netherlands
[3] Med Univ Harbin, Dept Gen Surg 3, Clin Hosp Harbin 1, Harbin 150001, Peoples R China
[4] Univ Erlangen Nurnberg, D-91058 Erlangen, Germany
关键词
STRAIL FUSION PROTEIN; ANTIGEN HMW-MAA; APOPTOSIS INDUCTION; MEDIATED APOPTOSIS; TUMOR; CELLS; SPECIFICITY; ACTIVATION; RECEPTORS; EGFR;
D O I
10.1186/1476-4598-9-301
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
Background: Advanced melanoma is characterized by a pronounced resistance to therapy leading to a limited patient survival of similar to 6 - 9 months. Here, we report on a novel bifunctional therapeutic fusion protein, designated anti-MCSP: TRAIL, that is comprised of a melanoma-associated chondroitin sulfate proteoglycan (MCSP)-specific antibody fragment (scFv) fused to soluble human TRAIL. MCSP is a well-established target for melanoma immunotherapy and has recently been shown to provide important tumorigenic signals to melanoma cells. TRAIL is a highly promising tumoricidal cytokine with no or minimal toxicity towards normal cells. Anti-MCSP: TRAIL was designed to 1. selectively accrete at the cell surface of MCSP-positive melanoma cells and inhibit MCSP tumorigenic signaling and 2. activate apoptotic TRAIL-signaling. Results: Treatment of a panel of MCSP-positive melanoma cell lines with anti-MCSP: TRAIL induced TRAIL-mediated apoptotic cell death within 16 h. Of note, treatment with anti-MCSP: sTRAIL was also characterized by a rapid dephosphorylation of key proteins, such as FAK, implicated in MCSP-mediated malignant behavior. Importantly, anti-MCSP: TRAIL treatment already inhibited anchorage-independent growth by 50% at low picomolar concentrations, whereas > 100 fold higher concentrations of non-targeted TRAIL failed to reduce colony formation. Daily i.v. treatment with a low dose of anti-MCSP: TRAIL (0.14 mg/kg) resulted in a significant growth retardation of established A375 M xenografts. Anti-MCSP: TRAIL activity was further synergized by co-treatment with rimcazole, a s-ligand currently in clinical trials for the treatment of various cancers. Conclusions: Anti-MCSP: TRAIL has promising pre-clinical anti-melanoma activity that appears to result from combined inhibition of tumorigenic MCSP-signaling and concordant activation of TRAIL-apoptotic signaling. Anti-MCSP: TRAIL alone, or in combination with rimcazole, may be of potential value for the treatment of malignant melanoma.
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页数:14
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