| Literature DB >> 12168839 |
Hironori Abe1, Motomu Kuroki, Katsuro Tachibana, Tieli Li, Aradhana Awasthi, Aruto Ueno, Hisanobu Matsumoto, Takayuki Imakiire, Yasushi Yamauchi, Hiromi Yamada, Asami Ariyoshi, Masahide Kuroki.
Abstract
The goal of this study was to develop a strategy for the selective destruction of cancer cells by ultrasonic irradiation in the presence of an antibody-conjugated photosensitizer. To this end, a photoimmunoconjugate (PIC) was prepared between ATX-70, a photosensitizer of a gallium-porphyrin analogue, and F11-39, a high affinity monoclonal antibody (MAb) against carcinoembryonic antigen (CEA), which is often overexpressed in various carcinoma cells. This conjugate, designated F39/ATX-70, retained immunoreactivity against purified CEA and CEA-expressing cells as determined by enzyme-linked immunosorbent assay, flow cytometry and immunofluorescence microscopic analysis. The cytotoxicity of F39/ATX-70 against CEA-expressing human gastric carcinoma cells in vitro was found to be greater than that of ATX-70 when applied in combination with ultrasound irradiation. When in vivo anti-tumor effects in a mouse xenograft model were assessed, intravenous administration of F39/ATX-70 followed by ultrasonic irradiation produced a marked growth inhibition of tumor compared with irradiation alone or irradiation after administration of ATX-70. These results suggest that the PIC between anti-CEA MAb and ATX-70 may have applications in sonodynamic therapy where destruction of CEA-expressing tumor is required.Entities:
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Year: 2002 PMID: 12168839
Source DB: PubMed Journal: Anticancer Res ISSN: 0250-7005 Impact factor: 2.480