Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Nov 20;12(11):3456.
doi: 10.3390/cancers12113456.

Molecular and Immune Biomarkers for Cutaneous Melanoma: Current Status and Future Prospects

Affiliations
Review

Molecular and Immune Biomarkers for Cutaneous Melanoma: Current Status and Future Prospects

Lorenzo Pilla et al. Cancers (Basel). .

Abstract

Advances in the genomic, molecular and immunological make-up of melanoma allowed the development of novel targeted therapy and of immunotherapy, leading to changes in the paradigm of therapeutic interventions and improvement of patients' overall survival. Nevertheless, the mechanisms regulating either the responsiveness or the resistance of melanoma patients to therapies are still mostly unknown. The development of either the combinations or of the sequential treatment of different agents has been investigated but without a strongly molecularly motivated rationale. The need for robust biomarkers to predict patients' responsiveness to defined therapies and for their stratification is still unmet. Progress in immunological assays and genomic techniques as long as improvement in designing and performing studies monitoring the expression of these markers along with the evolution of the disease allowed to identify candidate biomarkers. However, none of them achieved a definitive role in predicting patients' clinical outcomes. Along this line, the cross-talk of melanoma cells with tumor microenvironment plays an important role in the evolution of the disease and needs to be considered in light of the role of predictive biomarkers. The overview of the relationship between the molecular basis of melanoma and targeted therapies is provided in this review, highlighting the benefit for clinical responses and the limitations. Moreover, the role of different candidate biomarkers is described together with the technical approaches for their identification. The provided evidence shows that progress has been achieved in understanding the molecular basis of melanoma and in designing advanced therapeutic strategies. Nevertheless, the molecular determinants of melanoma and their role as biomarkers predicting patients' responsiveness to therapies warrant further investigation with the vision of developing more effective precision medicine.

Keywords: PD-1; biomarkers; checkpoint inhibitor; melanoma; target therapy.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest

Figures

Figure 1
Figure 1
Clinical applications of cancer biomarkers. Genetic, protein and cellular components can serve as diagnostic, prognostic, predictive and/or on-treatment biomarkers. diagnostic biomarker are used identify and detect the presence of cancer in individuals. Prognostic biomarkers provide information on the risk of recurrence and expected outcomes. Predictive biomarkers forecast the potential benefit of a specific treatment. On-treatment biomarker help to identify early progressors from long responders.

Similar articles

Cited by

References

    1. Siegel R.L., Mph K.D.M., Jemal A. Cancer statistics, 2017. CA Cancer J. Clin. 2017;67:7–30. doi: 10.3322/caac.21387. - DOI - PubMed
    1. Ascierto P.A., Flaherty K., Goff S. Emerging strategies in systemic therapy for the treatment of melanoma. Am. Soc. Clin. Oncol. Educ. B. 2018;38:751–758. doi: 10.1200/EDBK_199047. - DOI - PubMed
    1. Long G.V., Hauschild A., Santinami M., Atkinson V., Mandalà M., Chiarion-Sileni V., Larkin J., Nyakas M., Dutriaux C., Haydon A., et al. Adjuvant Dabrafenib plus Trametinib in stage IIIBRAF-mutated melanoma. N. Engl. J. Med. 2017;377:1813–1823. doi: 10.1056/NEJMoa1708539. - DOI - PubMed
    1. Weber J., Mandalà M., Del Vecchio M., Gogas H., Arance A.M., Cowey C.L., Dalle S., Schenker M., Chiarion-Sileni V., Marquez-Rodas I., et al. Adjuvant Nivolumab vs. Ipilimumab in resected stage III or IV melanoma. N. Engl. J. Med. 2017;377:1824–1835. doi: 10.1056/NEJMoa1709030. - DOI - PubMed
    1. Curtin J.A., Fridlyand J., Kageshita T., Patel H.N., Busam K.J., Kutzner H., Cho K.-H., Aiba S., Bröcker E.-B., LeBoit P.E., et al. Distinct sets of genetic alterations in melanoma. N. Engl. J. Med. 2005;353:2135–2147. doi: 10.1056/NEJMoa050092. - DOI - PubMed

LinkOut - more resources