: Non-melanoma skin cancer (NMSC), comprising basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC), represents the most common type of cancer worldwide, particularly among Caucasians. While BCC is locally invasive with minimal metastatic potential, cSCC is a highly aggressive tumor with a significant potential for metastasis, particularly in elderly populations. Tumor development and progression and the metastasis of cSCC are influenced by a complex interplay between tumor cells and the tumor microenvironment. Recent research highlights the importance of various immune cell subsets, including T cells, tumor-associated macrophages (TAMs), and dendritic cells, in influencing tumor progression, immune evasion, and treatment resistance. This review outlines key regulatory mechanisms in the immune tumor microenvironment (TME) of cSCC and explores the role of cytokines, immune checkpoints, and stromal interactions. We further discuss the relevance of three-dimensional (3D) in vitro models such as spheroids, organoids, and tumor-on-chip systems as tools to mimic immune-tumor interactions with higher physiological relevance, such as macrophage activation and polarization against cSCC cells. Globally, 3D models offer new opportunities for immunotherapy screening and mechanistic studies. Understanding the immune landscape in cSCC through advanced modeling techniques holds strong clinical potential for improving diagnostic and therapeutic strategies.

Exploring the complexity of cutaneous squamous cell carcinoma microenvironment. Focus on immune cell roles by novel 3D in vitro models / Quadri, Marika; Iuliano, Marco; Rosa, Paolo; Mangino, Giorgio; Palazzo, Elisabetta. - In: LIFE. - ISSN 2075-1729. - 15:8(2025). [10.3390/life15081170]

Exploring the complexity of cutaneous squamous cell carcinoma microenvironment. Focus on immune cell roles by novel 3D in vitro models

Iuliano, Marco;Rosa, Paolo;Mangino, Giorgio;
2025

Abstract

: Non-melanoma skin cancer (NMSC), comprising basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC), represents the most common type of cancer worldwide, particularly among Caucasians. While BCC is locally invasive with minimal metastatic potential, cSCC is a highly aggressive tumor with a significant potential for metastasis, particularly in elderly populations. Tumor development and progression and the metastasis of cSCC are influenced by a complex interplay between tumor cells and the tumor microenvironment. Recent research highlights the importance of various immune cell subsets, including T cells, tumor-associated macrophages (TAMs), and dendritic cells, in influencing tumor progression, immune evasion, and treatment resistance. This review outlines key regulatory mechanisms in the immune tumor microenvironment (TME) of cSCC and explores the role of cytokines, immune checkpoints, and stromal interactions. We further discuss the relevance of three-dimensional (3D) in vitro models such as spheroids, organoids, and tumor-on-chip systems as tools to mimic immune-tumor interactions with higher physiological relevance, such as macrophage activation and polarization against cSCC cells. Globally, 3D models offer new opportunities for immunotherapy screening and mechanistic studies. Understanding the immune landscape in cSCC through advanced modeling techniques holds strong clinical potential for improving diagnostic and therapeutic strategies.
2025
3D models; cutaneous squamous cell carcinoma; immune cells; immune evasion; immunotherapy; non-melanoma skin cancer; organoids; spheroids; tumor microenvironment; tumor-associated macrophages; tumor-on-chip
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Exploring the complexity of cutaneous squamous cell carcinoma microenvironment. Focus on immune cell roles by novel 3D in vitro models / Quadri, Marika; Iuliano, Marco; Rosa, Paolo; Mangino, Giorgio; Palazzo, Elisabetta. - In: LIFE. - ISSN 2075-1729. - 15:8(2025). [10.3390/life15081170]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1744793
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