» Articles » PMID: 35260531

Melanoma Therapeutics: a Literature Review

Overview
Journal J Biomed Res
Specialty General Medicine
Date 2022 Mar 9
PMID 35260531
Authors
Affiliations
Soon will be listed here.
Abstract

Melanoma is a relentless type of skin cancer which involves myriad signaling pathways which regulate many cellular processes. This makes melanoma difficult to treat, especially when identified late. At present, therapeutics include chemotherapy, surgical resection, biochemotherapy, immunotherapy, photodynamic and targeted approaches. These interventions are usually administered as either a single-drug or in combination, based on tumor location, stage, and patients' overall health condition. However, treatment efficacy generally decreases as patients develop treatment resistance. Genetic profiling of melanocytes and the discovery of novel molecular factors involved in the pathogenesis of melanoma have helped to identify new therapeutic targets. In this literature review, we examine several newly approved therapies, and briefly describe several therapies being assessed for melanoma. The goal is to provide a comprehensive overview of recent developments and to consider future directions in the field of melanoma.

Citing Articles

Novel Method for the Synthesis of Hydroxycobalamin[-lactam] and Its Impact on Melanoma Cells In Vitro.

Rzepka Z, Janus M, Marciniec K, Rok J, Wrzesniok D Int J Mol Sci. 2025; 26(4).

PMID: 40004003 PMC: 11855847. DOI: 10.3390/ijms26041540.


Preclinical pharmaco-toxicological screening of biomimetic melanin-like nanoparticles as a potential therapeutic strategy for cutaneous melanoma.

Marcovici I, Chioibas R, Zupko I, Pinzaru I, Moaca A, Ledeti A Front Pharmacol. 2025; 16:1487854.

PMID: 39981176 PMC: 11839674. DOI: 10.3389/fphar.2025.1487854.


Effect of Neutron Radiation on BPA-Loaded Melanoma Spheroids and Melanocytes.

Szczepanek M, Silarski M, Panek A, Telk A, Dziedzic-Kocurek K, Parisi G Cells. 2025; 14(3).

PMID: 39937023 PMC: 11816858. DOI: 10.3390/cells14030232.


Targeting Matrix Metalloproteinases and Their Inhibitors in Melanoma.

Szczygielski O, Dabrowska E, Niemyjska S, Przylipiak A, Zajkowska M Int J Mol Sci. 2025; 25(24.

PMID: 39769318 PMC: 11676509. DOI: 10.3390/ijms252413558.


Expert consensus on the diagnosis and treatment of solid tumors with BRAF mutations.

Wang W, Lian B, Xu C, Wang Q, Li Z, Zheng N Innovation (Camb). 2024; 5(6):100661.

PMID: 39529955 PMC: 11551471. DOI: 10.1016/j.xinn.2024.100661.


References
1.
Kawakami Y, Rosenberg S . T-cell recognition of self peptides as tumor rejection antigens. Immunol Res. 1996; 15(3):179-90. DOI: 10.1007/BF02918248. View

2.
Sharma P, Hu-Lieskovan S, Wargo J, Ribas A . Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy. Cell. 2017; 168(4):707-723. PMC: 5391692. DOI: 10.1016/j.cell.2017.01.017. View

3.
Wheatley K, Ives N, Hancock B, Gore M, Eggermont A, Suciu S . Does adjuvant interferon-alpha for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials. Cancer Treat Rev. 2003; 29(4):241-52. DOI: 10.1016/s0305-7372(03)00074-4. View

4.
Faramarzi S, Ghafouri-Fard S . Melanoma: a prototype of cancer-testis antigen-expressing malignancies. Immunotherapy. 2017; 9(13):1103-1113. DOI: 10.2217/imt-2017-0091. View

5.
Gasser S, Lim L, Cheung F . The role of the tumour microenvironment in immunotherapy. Endocr Relat Cancer. 2017; 24(12):T283-T295. DOI: 10.1530/ERC-17-0146. View