2020
DOI: 10.3390/ijms21238989
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RAGE Signaling in Melanoma Tumors

Abstract: Despite recent progresses in its treatment, malignant cutaneous melanoma remains a cancer with very poor prognosis. Emerging evidences suggest that the receptor for advance glycation end products (RAGE) plays a key role in melanoma progression through its activation in both cancer and stromal cells. In tumors, RAGE activation is fueled by numerous ligands, S100B and HMGB1 being the most notable, but the role of many other ligands is not well understood and should not be underappreciated. Here, we provide a rev… Show more

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Cited by 17 publications
(16 citation statements)
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References 267 publications
(336 reference statements)
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“…Numerous studies, ranging from clinical studies to molecular analyses, have highlighted a strong contribution of inflammation to the development of MM and other cancers. There is also evidence that the presence of inflammatory proteins in the tumor milieu, whether derived from intrinsic pathways of inflammation (melanoma cells) or extrinsic pathways (the preceding SARS-CoV-2 infection, other sources of innate immunity, genetics, tissue damage, or autoimmune disease) promote melanoma cell survival, proliferation, migration, angiogenesis, lymphangiogenesis, and invasion ( 14 19 , 23 – 26 ). These intrinsic and extrinsic pathways of inflammation also signal the development and accumulation of myeloid-derived suppressor cells and tumor-associated macrophages, which result in T-cell tolerance and suppression of the antitumor immune response, thereby facilitating tumor growth ( 24 , 27 29 ).…”
Section: Discussionmentioning
confidence: 99%
“…Numerous studies, ranging from clinical studies to molecular analyses, have highlighted a strong contribution of inflammation to the development of MM and other cancers. There is also evidence that the presence of inflammatory proteins in the tumor milieu, whether derived from intrinsic pathways of inflammation (melanoma cells) or extrinsic pathways (the preceding SARS-CoV-2 infection, other sources of innate immunity, genetics, tissue damage, or autoimmune disease) promote melanoma cell survival, proliferation, migration, angiogenesis, lymphangiogenesis, and invasion ( 14 19 , 23 – 26 ). These intrinsic and extrinsic pathways of inflammation also signal the development and accumulation of myeloid-derived suppressor cells and tumor-associated macrophages, which result in T-cell tolerance and suppression of the antitumor immune response, thereby facilitating tumor growth ( 24 , 27 29 ).…”
Section: Discussionmentioning
confidence: 99%
“…The RAGE/ligand axis appears to support the association between chronic inflammation and immunosuppression. Therefore, targeting RAGE in melanoma tumors could be therapeutically beneficial [26].…”
Section: Prognostic Tissue Biomarkersmentioning
confidence: 99%
“…AGEs have been shown to increase melanoma cell proliferation and migration, tumor growth, and metastasis through the interaction with their receptor (RAGE) on the melanoma cell surface. The blockade of the AGE/RAGE axis prevents tumor growth and inhibits angiogenesis [56].…”
Section: Red and Processed Meatmentioning
confidence: 99%