Department of Molecular Biology of Cancer, Medical University of Lodz, 6/8 Mazowiecka Street, 92-215 Lodz, Poland.
Int J Mol Sci. 2020 Apr 23;21(8):2980. doi: 10.3390/ijms21082980.
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 BRAF 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.
抵抗细胞死亡是癌症的一个标志。细胞死亡程序执行的紊乱促进了致癌作用和癌细胞在不利条件下的存活,包括暴露于抗癌治疗中。根据不同的标准,已经对特定形式的调节性细胞死亡 (RCD) 进行了分类,包括形态特征、生化改变和免疫学后果。尽管黑色素瘤细胞广泛配备了抗细胞凋亡机制,并且 RAS/RAF/MEK/ERK 信号转导组件中的反复遗传改变显著促成了黑色素瘤的生存表型,但自噬依赖性细胞死亡、坏死性凋亡、铁死亡、细胞焦亡和 parthanatos 的作用最近引起了极大的兴趣。这些信号级联参与了黑色素瘤细胞对临床中使用的治疗药物的反应和耐药性,包括 BRAF 和 MEK1/2 抑制剂以及免疫疗法。此外,还证明了对非细胞凋亡性细胞死亡途径的敏感性与特定细胞表型之间的关系,这表明可以利用黑色素瘤细胞的可塑性来调节这些细胞对不同细胞死亡刺激的反应。在这篇综述中,讨论了黑色素瘤细胞生物学中非细胞凋亡性细胞死亡信号通路以及对抗癌药物的反应的最新知识。