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
- drug delivery
- papillary thyroid
- platelet rich plasma
- skin cancer
- cell cycle
- single molecule
- peripheral blood
- current status
- squamous cell
- squamous cell carcinoma
- risk assessment
- lymph node metastasis
- mesenchymal stem cells
- cell proliferation
- basal cell carcinoma
- multiple myeloma
- highly efficient
- wound healing
- binding protein
- case control