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Recombinant TSR1 of ADAMTS5 Suppresses Melanoma Growth in Mice via an Anti-angiogenic Mechanism.

Cancers (Basel). 2018; 
Renganathan Bhuvanasundar,Durairaj Vinoth,Kirman Dogan Can,Esubonteng Paa Kow A,Ang Swee Kim,Ge Ru
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Codon Optimization The TSR1 domain of human ADAMTS5 corresponds to amino acid residues 567–622. The cDNA sequence corresponding to residues 561–634, which include the surrounding sequences on both the Nand C-terminus of TSR1, were codon-optimized for E. coli expression and cloned into a pET30a vector with a N-terminal His-tag (GenScript, Piscataway, NJ, USA). The membrane was blocked with 3% skimmed milk for 1 h at room temperature. This was followed by overnight incubation with an anti-His antibody (Cat # A00186-100, GenScript, Piscataway, NJ, USA), probing with the respective fluorescent tagged secondary antibody (Cat # 926-32212, LICOR Inc., Lincoln, NE, USA), and visualization using a fluorescent imaging system (Odyssey CLx, LI-COR Inc.). Get A Quote

摘要

Inhibiting tumor angiogenesis is a well-established approach for anticancer therapeutic development. A Disintegrin-like and Metalloproteinase with ThromboSpondin Motifs 5 (ADAMTS5) is a secreted matrix metalloproteinase in the ADAMTS family that also functions as an anti-angiogenic/anti-tumorigenic molecule. Its anti-angiogenic/anti-tumorigenic function is independent from its proteinase activity, but requires its first thrombospondin type 1 repeat (TSR1). However, it is not known if recombinant TSR1 (rTSR1) can function as an anticancer therapeutic. In this report, we expressed and purified a 75-residue recombinant TSR1 polypeptide from and investigated its ability to function as an anticancer therapeut... More

關鍵詞

ADAMTS5,TSR1,anti-angiogenic,anticancer,apopt
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