AI Article Synopsis

  • 5-Aminolevulinic acid (5-ALA) can be converted into protoporphyrin IX (PpIX) in tumor cells, allowing for effective photodynamic therapy (PDT), but some tumors convert PpIX into heme, reducing its effectiveness.
  • Researchers developed a polymeric iron chelator to remove excess labile iron within tumors, which enhanced PpIX accumulation and increased the cytotoxic effects of PDT in cancer cells.
  • In animal studies, this chelator improved PpIX buildup and the overall effectiveness of PDT, indicating its potential as a valuable tool in cancer treatment.

Article Abstract

5-Aminolevulinic acid (5-ALA) is an amino acid that can be metabolized into a photosensitizer, protoporphyrin IX (PpIX) selectively in a tumor cell, permitting minimally invasive photodynamic diagnosis/therapy. However, some malignant tumor cells have excess intracellular labile iron and facilitate the conversion of PpIX into heme, which compromises the therapeutic potency of 5-ALA. Here, we examined the potential of chelation of such unfavorable intratumoral labile iron in photodynamic therapy (PDT) with 5-ALA hydrochloride, using polymeric iron chelators that we recently developed. The polymeric iron chelator efficiently inactivated the intracellular labile iron in cultured cancer cells and importantly enhanced the accumulation of PpIX, thereby improving the cytotoxicity upon photoirradiation. Even in in vivo study with subcutaneous tumor models, the polymeric iron chelator augmented the intratumoral accumulation of PpIX and the PDT effect. This study suggests that our polymeric iron chelator could be a tool for boosting the effect of 5-ALA-induced PDT by modulating tumor microenvironment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986068PMC
http://dx.doi.org/10.1111/cas.15637DOI Listing

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