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Author Spotlight: Recreating Melanoma Complexity with Patient-Derived Organoids for Immunotherapy Evaluation
Published on: September 6, 2024
Unveiling the Dynamic Interplay between Cancer Stem Cells and the Tumor Microenvironment in Melanoma: Implications
Patrizia Limonta1, Raffaella Chiaramonte2, Lavinia Casati2
1Department of Pharmacological and Biomolecular Sciences "R. Paoletti", Università degli Studi di Milano, 20133 Milan, Italy.
Abstract:
Cutaneous melanoma still represents a significant health burden worldwide, being responsible for the majority of skin cancer deaths. Key advances in therapeutic strategies have significantly improved patient outcomes; however, most patients experience drug resistance and tumor relapse. Cancer stem cells (CSCs) are a small subpopulation of cells in different tumors, including melanoma, endowed with distinctive capacities of self-renewal and differentiation into bulk tumor cells. Melanoma CSCs are characterized by the expression of specific biomarkers and intracellular pathways; moreover, they play a pivotal role in tumor onset, progression and drug resistance. In recent years, great efforts have been made to dissect the molecular mechanisms underlying the protumor activities of melanoma CSCs to provide the basis for novel CSC-targeted therapies. Herein, we highlight the intricate crosstalk between melanoma CSCs and bystander cells in the tumor microenvironment (TME), including immune cells, endothelial cells and cancer-associated fibroblasts (CAFs), and its role in melanoma progression. Specifically, we discuss the peculiar capacities of melanoma CSCs to escape the host immune surveillance, to recruit immunosuppressive cells and to educate immune cells toward an immunosuppressive and protumor phenotype. We also address currently investigated CSC-targeted strategies that could pave the way for new promising therapeutic approaches for melanoma care.
Insights
Melanoma cancer stem cells (CSCs) drive tumor growth and drug resistance by interacting with the tumor microenvironment. Targeting these CSCs and their interactions offers new therapeutic strategies for melanoma.
Area of Science:
- Oncology
- Cancer Biology
- Immunology
Background:
- Cutaneous melanoma is a major cause of skin cancer mortality worldwide.
- Despite therapeutic advances, drug resistance and tumor relapse remain significant challenges.
- Melanoma cancer stem cells (CSCs) are crucial for tumor initiation, progression, and resistance.
Purpose of the Study:
- To elucidate the molecular mechanisms of melanoma CSCs.
- To highlight the role of melanoma CSCs in the tumor microenvironment (TME).
- To explore novel CSC-targeted therapies for melanoma.
Main Methods:
- Review of current literature on melanoma CSCs and their TME interactions.
- Analysis of CSC biomarkers and intracellular pathways.
- Discussion of immune evasion and modulation by melanoma CSCs.
Main Results:
- Melanoma CSCs interact with immune cells, endothelial cells, and cancer-associated fibroblasts (CAFs).
- CSCs possess unique abilities to evade immune surveillance and promote immunosuppression.
- These interactions contribute to melanoma progression and therapeutic resistance.
Conclusions:
- Melanoma CSCs are key drivers of disease progression and treatment failure.
- Understanding CSC-TME crosstalk is vital for developing effective melanoma therapies.
- Targeting melanoma CSCs and their microenvironment interactions holds promise for future treatments.
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