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**Ad-MCP1-tk** is an experimental bicistronic recombinant adenoviral cancer gene-therapy vector designed for hepatocellular carcinoma. It expresses **monocyte chemoattractant protein-1** and **herpes simplex virus thymidine kinase** from a CAG promoter through an internal ribosomal entry site, with MCP-1 positioned upstream of HSV-tk. HSV-tk sensitizes transduced tumor cells to ganciclovir-mediated cytotoxicity, while MCP-1 promotes macrophage recruitment and macrophage-associated tumor necrosis factor-alpha production. In preclinical hepatocellular carcinoma models, Ad-MCP1-tk was less effective at suppressing tumor growth than the reverse-order vector Ad-tk-MCP1.
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