Innate Immune Cells in Melanoma: Implications for Immunotherapy.
Marialuisa TrocchiaAnnagioia VentriciLuca ModestinoLeonardo CristinzianoAnne Lise FerraraFrancesco PalestraStefania LoffredoMariaelena CaponeGabriele MadonnaMarilena RomanelliPaolo Antonio AsciertoMaria Rosaria GaldieroPublished in: International journal of molecular sciences (2024)
The innate immune system, composed of neutrophils, basophils, eosinophils, myeloid-derived suppressor cells (MDSCs), macrophages, dendritic cells (DCs), mast cells (MCs), and innate lymphoid cells (ILCs), is the first line of defense. Growing evidence demonstrates the crucial role of innate immunity in tumor initiation and progression. Several studies support the idea that innate immunity, through the release of pro- and/or anti-inflammatory cytokines and tumor growth factors, plays a significant role in the pathogenesis, progression, and prognosis of cutaneous malignant melanoma (MM). Cutaneous melanoma is the most common skin cancer, with an incidence that rapidly increased in recent decades. Melanoma is a highly immunogenic tumor, due to its high mutational burden. The metastatic form retains a high mortality. The advent of immunotherapy revolutionized the therapeutic approach to this tumor and significantly ameliorated the patients' clinical outcome. In this review, we will recapitulate the multiple roles of innate immune cells in melanoma and the related implications for immunotherapy.
Keyphrases
- innate immune
- skin cancer
- induced apoptosis
- cell cycle arrest
- dendritic cells
- immune response
- risk factors
- end stage renal disease
- cell death
- signaling pathway
- endoplasmic reticulum stress
- newly diagnosed
- cardiovascular disease
- chronic kidney disease
- pi k akt
- prognostic factors
- cell proliferation
- cardiovascular events
- regulatory t cells
- peritoneal dialysis
- patient reported outcomes
- basal cell carcinoma
- patient reported
- case control