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Related Concept Videos

Skin Cancer01:30

Skin Cancer

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Skin cancer is a type of cancer that occurs when there is an abnormal growth of skin cells, usually triggered by damage to the DNA within the skin cells. It is primarily caused by exposure to ultraviolet (UV) radiation from the sun or artificial sources like tanning beds. Skin cancer is the most common type of cancer worldwide, and its incidence continues to rise.
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The color of the skin is influenced by a number of pigments, including melanin, carotene, and hemoglobin. Recall that melanin is produced by cells called melanocytes, which are found scattered throughout the stratum basale of the epidermis. The melanin is transferred to the keratinocytes via melanosomes.
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A 3D Organotypic Melanoma Spheroid Skin Model
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A 3D Organotypic Melanoma Spheroid Skin Model

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Melanoma.

Dirk Schadendorf1,2, David E Fisher3, Claus Garbe2,4

  • 1Department of Dermatology, University Duisburg-Essen, University Hospital Essen, Hufelandstrasse 55, 45147 Essen, Germany.

Nature Reviews. Disease Primers
|May 19, 2016
PubMed
Summary
This summary is machine-generated.

Melanoma incidence is rising, with sun exposure as a key risk factor. Advances in understanding genetic mutations and developing targeted therapies like BRAF inhibitors and PD1-specific antibodies are significantly improving patient prognosis and quality of life.

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Area of Science:

  • Oncology
  • Dermatology
  • Genetics

Background:

  • Melanoma is a prevalent and increasing cancer in Western countries.
  • Sun exposure is the primary risk factor, but genetic alterations also play a crucial role.
  • Early detection campaigns have reduced mortality rates.

Purpose of the Study:

  • To summarize current understanding of melanoma, covering mechanistic insights and clinical progress.
  • To highlight the significance of genetic mutations in melanoma development and treatment.
  • To review recent therapeutic advancements and their impact on patient outcomes.

Main Methods:

  • Review of current scientific literature on melanoma.
  • Analysis of genetic alterations associated with different melanoma subtypes.
  • Evaluation of novel therapeutic strategies, including targeted therapies and immunotherapies.

Main Results:

  • Key genetic mutations identified include BRAF, NRAS, KIT, GNAQ, GNA11, and alterations in the PI3K-AKT-PTEN and immune checkpoint pathways.
  • Programmed cell death protein 1 (PD1) pathway inhibitors (e.g., nivolumab, pembrolizumab) show promise.
  • BRAF and MEK inhibitors have significantly improved outcomes for advanced-stage metastatic melanoma.

Conclusions:

  • Understanding melanoma's genetic landscape is critical for effective treatment.
  • Novel therapies are transforming melanoma prognosis, improving long-term benefits and quality of life.
  • Continued research into melanoma mechanisms and treatments is essential.