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Updated: May 11, 2026

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
Signal transduction in human cutaneous melanoma and target drugs
Anatoly B Uzdensky1, Svetlana V Demyanenko, Mikhail Y Bibov
1194/1 Stachky ave., NII NK, Rostov-on-Don, 344090, Russia. auzd@yandex.ru.
Abstract:
Malignant melanoma is an extremely aggressive and metastatic cancer, highly resistant to conventional treatment modalities. Understanding of fundamental mechanisms responsible for its genesis and progression is critical for development of successful chemotherapeutic treatment. It is becoming clear that melanoma results from complex changes in multiple signaling pathways that control cell proliferation and ability to evade the cell death processes. Impairment or hyper-activation of some components of these pathways may lead to malignant transformation and cancer development. In the present review we consider the current data on involvement of such signaling pathways as cyclin/CDK, Ras/Raf/MEK/MAPK, JNK/c-Jun/AP-1, PI3K/Akt/PTEN/mTOR, IKK/I-κB/NF-κB, Wnt/β-catenin, Notch, Jak/STAT, MITF and some growth factors in regulation of the cell cycle progression, apoptosis and development of human cutaneous melanoma. Understanding of molecular aberrations that underlie melanoma oncogenesis is essential for improvement of diagnosis, accurate prognosis assessment, and rational design of effective therapeutics. Inhibitors of these pathways may serve as promising tools for anti-melanoma targeted therapy. Some novel anti-melanoma target drugs are characterized.
Insights
Malignant melanoma arises from complex signaling pathway changes affecting cell growth and survival. Targeting these pathways offers promising new therapeutic strategies for this aggressive cancer.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- Malignant melanoma is an aggressive, metastatic cancer resistant to conventional treatments.
- Understanding melanoma's underlying molecular mechanisms is crucial for developing effective therapies.
- Melanoma development involves intricate alterations in signaling pathways controlling cell proliferation and apoptosis.
Purpose of the Study:
- To review current data on signaling pathways involved in human cutaneous melanoma development.
- To highlight the role of these pathways in cell cycle regulation and apoptosis evasion.
- To discuss the potential of targeting these pathways for melanoma treatment.
Main Methods:
- Literature review of current scientific data on melanoma signaling pathways.
- Analysis of pathways including cyclin/CDK, Ras/Raf/MEK/MAPK, PI3K/Akt/PTEN/mTOR, and others.
- Examination of growth factor involvement in melanoma pathogenesis.
Main Results:
- Multiple signaling pathways (e.g., Ras/Raf/MEK/MAPK, PI3K/Akt/PTEN/mTOR, Wnt/β-catenin) are implicated in melanoma genesis and progression.
- Dysregulation of these pathways contributes to uncontrolled cell proliferation and resistance to cell death.
- Specific pathways like MITF and Jak/STAT also play significant roles.
Conclusions:
- Understanding molecular aberrations in melanoma oncogenesis is key for improved diagnosis and prognosis.
- Targeted inhibitors of these signaling pathways represent a promising strategy for anti-melanoma therapy.
- Novel targeted drugs are being developed based on these molecular insights.
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