Exploring the Complex and Multifaceted Interplay between Melanoma Cells and the Tumor Microenvironment

被引:7
作者
Kuras, Magdalena [1 ,2 ]
机构
[1] Lund Univ, Dept Biomed Engn, S-22100 Lund, Sweden
[2] Lund Univ, Dept Translat Med, Sect Clin Chem, S-20502 Malmo, Sweden
关键词
malignant melanoma; tumor microenvironment; metabolic reprogramming; phenotype switching; cellular plasticity; molecular classifications; mutational burden; treatment resistance; IMMUNE CHECKPOINT INHIBITORS; METASTATIC MELANOMA; THERAPEUTIC TARGETS; SIGNALING PATHWAYS; PROFILING REVEALS; MC1R VARIANTS; MAPK PATHWAY; T-CELLS; N-RAS; EXPRESSION;
D O I
10.3390/ijms241814403
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malignant melanoma is a very aggressive skin cancer, characterized by a heterogeneous nature and high metastatic potential. The incidence of melanoma is continuously increasing worldwide, and it is one of the most common cancers in young adults. In the past twenty years, our understanding of melanoma biology has increased profoundly, and disease management for patients with disseminated disease has improved due to the emergence of immunotherapy and targeted therapy. However, a significant fraction of patients relapse or do not respond adequately to treatment. This can partly be explained by the complex signaling between the tumor and its microenvironment, giving rise to melanoma phenotypes with different patterns of disease progression. This review focuses on the key aspects and complex relationship between pathogenesis, genetic abnormalities, tumor microenvironment, cellular plasticity, and metabolic reprogramming in melanoma. By acquiring a deeper understanding of the multifaceted features of melanomagenesis, we can reach a point of more individualized and patient-centered disease management and reduced costs of ineffective treatments.
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页数:22
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