Abstract

Resisting cell death is a hallmark of cancer. Disturbances in the execution of cell death programs promote carcinogenesis and survival of cancer cells under unfavorable conditions, including exposition to anti-cancer therapies. Specific modalities of regulated cell death (RCD) have been classified based on different criteria, including morphological features, biochemical alterations and immunological consequences. Although melanoma cells are broadly equipped with the anti-apoptotic machinery and recurrent genetic alterations in the components of the RAS/RAF/MEK/ERK signaling markedly contribute to the pro-survival phenotype of melanoma, the roles of autophagy-dependent cell death, necroptosis, ferroptosis, pyroptosis, and parthanatos have recently gained great interest. These signaling cascades are involved in melanoma cell response and resistance to the therapeutics used in the clinic, including inhibitors of BRAFmut and MEK1/2, and immunotherapy. In addition, the relationships between sensitivity to non-apoptotic cell death routes and specific cell phenotypes have been demonstrated, suggesting that plasticity of melanoma cells can be exploited to modulate response of these cells to different cell death stimuli. In this review, the current knowledge on the non-apoptotic cell death signaling pathways in melanoma cell biology and response to anti-cancer drugs has been discussed.

Highlights

  • Cell death is an essential biological process that controls development and homeostasis in the organism [1,2]

  • It is evident that melanoma cells utilize multiple mechanisms to counteract cell death-inducing signals, and the intersections between different signaling pathways involved in the regulation of cell survival and death are presumably a reason for a failure in melanoma response to potentially pro-death triggers

  • The landscape of regulated cell death modalities is still enlarging, and the role of non-apoptotic cell death signaling pathways have been given increasing attention in melanoma. This is further exemplified by parthanatos, which is a modality of cell death initiated by hyperactivation of poly(ADP-ribose) polymerase 1 (PARP1) that results in depletion of both NAD+ and ATP, and accumulation of poly(ADP-ribosyl)ated proteins in the mitochondria [5,229,230]

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Summary

Introduction

Cell death is an essential biological process that controls development and homeostasis in the organism [1,2]. Despite a tremendous advances in the therapeutic options for melanoma patients (Figure 1), inability or limited vulnerability of melanoma cells to induction of apoptosis in response to inhibitors of BRAFmut (BRAFi) and MEK (MEKi) [31,32,33,34,35,36,37,38], and escape from immunotherapy [39,40,41] are the reasons for re-growth of drug-resistant disease In this respect, research on the mechanisms of the non-apoptotic cell death modalities is attractive in melanoma. Mechanisms of autophagy regulation that have been shown in melanoma are included

Autophagy in Melanoma
An Overview of Necroptotic Signaling Pathway
Necroptosis in Melanoma
An Overview of Ferroptosis
Ferroptosis in Melanoma
An Overview of Pyroptosis
Pyroptosis in Melanoma
Findings
Conclusions and Future Directions
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