Nanobody-Targeted Photodynamic Therapy Selectively Kills Viral GPCR-Expressing Glioblastoma Cells.
Timo W M De GroofVida MashayekhiTian Shu FanNick D BergkampJavier Sastre TorañoJeffrey R van SentenRaimond HeukersMartine J SmitSabrina OliveiraPublished in: Molecular pharmaceutics (2019)
Photodynamic therapy (PDT) eradicates tumors by the local activation of a photosensitizer with near-infrared light. One of the aspects hampering the clinical use of PDT is the poor selectivity of the photosensitizer. To improve this, we have recently introduced a new approach for targeted PDT by conjugating photosensitizers to nanobodies. Diverse G protein-coupled receptors (GPCRs) show aberrant overexpression in tumors and are therefore interesting targets in cancer therapy. Here we show that GPCR-targeting nanobodies can be used in targeted PDT. We have developed a nanobody binding the extracellular side of the viral GPCR US28, which is detected in tumors like glioblastoma. The nanobody was site-directionally conjugated to the water-soluble photosensitizer IRDye700DX. This nanobody-photosensitizer conjugate selectively killed US28-expressing glioblastoma cells both in 2D and 3D cultures upon illumination with near-infrared light. This is the first example employing a GPCR as target for nanobody-directed PDT. With the emerging role of GPCRs in cancer, this data provides a new angle for exploiting this large family of receptors for targeted therapies.
Keyphrases
- photodynamic therapy
- cancer therapy
- drug delivery
- induced apoptosis
- fluorescence imaging
- water soluble
- cell cycle arrest
- sars cov
- endoplasmic reticulum stress
- cell proliferation
- papillary thyroid
- high resolution
- squamous cell carcinoma
- oxidative stress
- big data
- young adults
- pi k akt
- artificial intelligence
- lymph node metastasis
- childhood cancer