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Review
. 2018 Aug;13(4):437-446.
doi: 10.1007/s11523-018-0565-2.

The Role of Autophagy in the Resistance to BRAF Inhibition in BRAF-Mutated Melanoma

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Review

The Role of Autophagy in the Resistance to BRAF Inhibition in BRAF-Mutated Melanoma

Xiao Liu et al. Target Oncol. 2018 Aug.

Abstract

Malignant melanoma is the most aggressive and notorious skin cancer, and metastatic disease is associated with very poor long-term survival outcomes. Although metastatic melanoma patients with oncogenic mutations in the BRAF gene initially respond well to the treatment with specific BRAF inhibitors, most of them will eventually develop resistance to this targeted therapy. As a highly conserved catabolic process, autophagy is responsible for the maintenance of cellular homeostasis and cell survival, and is involved in multiple diseases, including cancer. Recent study results have indicated that autophagy might play a decisive role in the resistance to BRAF inhibitors in BRAF-mutated melanomas. In this review, we will discuss how autophagy is up-regulated by BRAF inhibitors, and how autophagy induces the resistance to these agents.

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References

    1. Cancer Discov. 2015 Apr;5(4):410-23 - PubMed
    1. EMBO J. 2016 Feb 1;35(3):281-301 - PubMed
    1. J Immunol. 2010 Sep 1;185(5):3028-34 - PubMed
    1. Cancer Cell Int. 2013 Aug 06;13(1):78 - PubMed
    1. Annu Rev Nutr. 2007;27:19-40 - PubMed

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