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Abstract

Cutaneous melanoma is a common cancer in Australia and New Zealand, Europe, and North America, and its incidence is still increasing in many regions. Ultraviolet (UV) radiation exposure (for example, through excessive sunlight exposure) remains the primary risk factor for melanoma; however, public awareness campaigns have led to a marked reduction in mortality. In addition to genetic damage from UV radiation, specific genetic alterations have been linked to melanoma. The stage of the tumour at the time of diagnosis is of greater importance for melanoma prognosis than in almost any other cancer. Context-dependent genetic mutations that attenuate tumour-suppressive mechanisms or activate growth-promoting signalling pathways are crucial factors in the development of cutaneous melanoma. In addition to external factors such as UV radiation, the tumour microenvironment can contribute to melanoma progression, invasion and metastasis. Cutaneous melanoma treatment has improved considerably over the past decade with the discovery and development of immune checkpoint inhibitors and therapy targeting BRAF and MEK. Over the next decade, several priorities are likely to influence melanoma research and management, including the continued advance of precision medicine methods to identify the most suitable patients for the most effective treatment, with the aim of improving clinical outcomes.

OriginalspracheEnglisch
Aufsatznummer23
ZeitschriftNature reviews. Disease primers
Jahrgang11
Ausgabenummer1
Seiten (von - bis)23
Seitenumfang1
DOIs
PublikationsstatusVeröffentlicht - 03.04.2025

Fördermittel

The authors thank C. Carrera, K. Liopiris, J. Malvehy and P. Zaballos (all from Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain) for providing the images in Figs. 5, 6 and 7 for this article. The authors extend their sincere gratitude to the patients who provided consent to publish their images in this Primer. A.T. acknowledges the support of an Emmy Noether Award from the German Research Foundation (DFG, 467788900) and the Ministry of Culture and Science of the State of North Rhine-Westphalia (NRW-Nachwuchsgruppenprogramm). A.T. acknowledges the support of an ERC starting grant (METATARGET, 101078355). A.T. holds the Peter Hans Hofschneider endowed Professorship of Molecular Medicine from the Stiftung Experimentelle Biomedizin.

TrägerTrägernummer
Stiftung Experimentelle Biomedizin
Ministerium für Kultur und Wissenschaft des Landes Nordrhein-Westfalen
NRW-Nachwuchsgruppenprogramm
Universitat de Barcelona
Deutsche Forschungsgemeinschaft467788900
European Research Council101078355
Novartis
BMS
Bayer HealthCare Pharmaceuticals Inc.
Merck Serono
Merck
Amgen
ISDIN

    UN SDGs

    Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

    1. SDG 3 – Gesundheit und Wohlergehen
      SDG 3 – Gesundheit und Wohlergehen

    Strategische Forschungsbereiche und Zentren

    • Profilbereich: Zentrum für Bevölkerungsmedizin und Versorgungsforschung (ZBV)
    • Profilbereich: Lübeck Integrated Oncology Network (LION)

    DFG-Fachsystematik

    • 2.22-19 Dermatologie
    • 2.22-14 Hämatologie, Onkologie
    • 2.22-02 Public Health, gesundheitsbezogene Versorgungsforschung, Sozial- und Arbeitsmedizin

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