AI Article Synopsis

  • The study focuses on using a genetically engineered immunotoxin, 4D5scFv-miniSOG, to selectively target and kill HER2-positive breast cancer cells.
  • The 4D5scFv miniSOG utilizes a single-chain variable fragment of an antibody to bind to the HER2 receptor, allowing for specific recognition and internalization by cancer cells.
  • The research shows that this targeted approach effectively induces cell death and enhances the effects of existing chemotherapy drugs like Taxol.

Article Abstract

Tumor-targeted delivery of cytotoxins presents considerable advantages over their passive transport. Chemical conjugation of cytotoxic module to antibody is limited due to insufficient reproducibility of synthesis, and recombinant immunotoxins are aimed to overcome this disadvantage. We obtained genetically encoded immunophotosensitizer 4D5scFv-miniSOG and evaluated its photocytotoxic effect in vitro. A single-chain variable fragment (scFv) of humanized 4D5 antibody was used as a targeting vehicle for selective recognition of the extracellular domain of human epidermal growth factor receptor 2 (HER2/neu) overexpressed in many human carcinomas. As a phototoxic module we used a recently described photoactivated fluorescent flavoprotein miniSOG. We found that recombinant protein 4D5scFv-miniSOG exerts a highly specific photo-induced cytotoxic effect on HER2/neu-positive human breast adenocarcinoma SK-BR-3 cells (IC50= 160 nM). We demonstrated that the 4D5scFv-miniSOG specifically binds to HER2-positive cells and internalizes via receptor-mediated endocytosis. Co-treatment of breast cancer cells with 4D5scFv-miniSOG and Taxol or junction opener protein JO-1 produced remarkable additive effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841334PMC
http://dx.doi.org/10.7150/thno.6715DOI Listing

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