From Molecular Biology to Novel Immunotherapies and Nanomedicine in Uveal Melanoma.
Kamil Jozef SynoradzkiNatalia PaduszyńskaMalgorzata SolnikMario Domenico ToroKrzysztof BilminElżbieta BylinaPiotr Lukasz RutkowskiYacoub A YousefClaudio BucoloSandrine Anne ZweifelMichele ReibaldiMichał FiedorowiczAnna Małgorzata CzarneckaPublished in: Current oncology (Toronto, Ont.) (2024)
Molecular biology studies of uveal melanoma have resulted in the development of novel immunotherapy approaches including tebentafusp-a T cell-redirecting bispecific fusion protein. More biomarkers are currently being studied. As a result, combined immunotherapy is being developed as well as immunotherapy with bifunctional checkpoint inhibitory T cell engagers and natural killer cells. Current trials cover tumor-infiltrating lymphocytes (TIL), vaccination with IKKb-matured dendritic cells, or autologous dendritic cells loaded with autologous tumor RNA. Another potential approach to treat UM could be based on T cell receptor engineering rather than antibody modification. Immune-mobilizing monoclonal T cell receptors (TCR) against cancer, called ImmTAC TM molecules, represent such an approach. Moreover, nanomedicine, especially miRNA approaches, are promising for future trials. Finally, theranostic radiopharmaceuticals enabling diagnosis and therapy with the same molecule bring hope to this research.
Keyphrases
- dendritic cells
- regulatory t cells
- natural killer cells
- cancer therapy
- immune response
- cell therapy
- bone marrow
- dna damage
- platelet rich plasma
- papillary thyroid
- photodynamic therapy
- skin cancer
- current status
- single molecule
- squamous cell carcinoma
- peripheral blood
- stem cells
- multiple myeloma
- young adults
- oxidative stress
- mesenchymal stem cells
- case control
- childhood cancer
- metal organic framework
- climate change