| Literature DB >> 19022220 |
Kiyotaka Nakano1, Tetsuro Orita, Junichi Nezu, Takeshi Yoshino, Iwao Ohizumi, Masamichi Sugimoto, Koh Furugaki, Yasuko Kinoshita, Takahiro Ishiguro, Takao Hamakubo, Tatsuhiko Kodama, Hiroyuki Aburatani, Hisafumi Yamada-Okabe, Masayuki Tsuchiya.
Abstract
Glypican 3 (GPC3), a GPI-anchored heparan sulfate proteoglycan, is expressed in the majority of hepatocellular carcinoma (HCC) tissues. Using MRL/lpr mice, we successfully generated a series of anti-GPC3 monoclonal antibodies (mAbs). GPC3 was partially cleaved between Arg358 and Ser359, generating a C-terminal 30-kDa fragment and an N-terminal 40-kDa fragment. All mAbs that induced antibody-dependent cellular cytotoxicity (ADCC) and/or complement-dependent cytotoxicity (CDC) against cells expressing GPC3 recognized the 30-kDa fragment, indicating that the C-terminal region of GPC3 serves as an epitope for mAb with ADCC and/or CDC inducing activities. Chimeric mAbs with Fc replaced by human IgG1 were created from GC33, one of the mAbs that reacted with the C-terminal 30-kDa fragment. Chimeric GC33 induced not only ADCC against GPC3-positive human HCC cells but also was efficacious against the Huh-7 human HCC xenograft. Thus, mAbs against the C-terminal 30-kDa fragment such as GC33 are useful in therapy targeting HCC.Entities:
Mesh:
Substances:
Year: 2008 PMID: 19022220 DOI: 10.1016/j.bbrc.2008.11.033
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575