Department of Cell Pathology, Faculty of Biotechnology, University of Wroclaw, Joliot-Curie 14a, 50-383 Wroclaw, Poland.
Department of Oncology and Division of Surgical Oncology, Wroclaw Medical University, Plac Hirszfelda 12, 53-413 Wroclaw, Poland.
Int J Mol Sci. 2020 Nov 7;21(21):8359. doi: 10.3390/ijms21218359.
The low efficiency of currently-used anti-cancer therapies poses a serious challenge, especially in the case of malignant melanoma, a cancer characterized by elevated invasiveness and relatively high mortality rate. The role of the tumor microenvironment in the progression of melanoma and its acquisition of resistance to treatment seems to be the main focus of recent studies. One of the factors that, in normal conditions, aids the organism in its fight against the cancer and, following the malignant transformation, adapts to facilitate the development of the tumor is the immune system. A variety of cell types, i.e., T and B lymphocytes, macrophages, and dendritic and natural killer cells, as well as neutrophils, support the growth and invasiveness of melanoma cells, utilizing a plethora of mechanisms, including secretion of pro-inflammatory molecules, induction of inhibitory receptors expression, or depletion of essential nutrients. This review provides a comprehensive summary of the processes regulated by tumor-associated cells that promote the immune escape of melanoma cells. The described mechanisms offer potential new targets for anti-cancer treatment and should be further studied to improve currently-employed therapies.
目前使用的抗癌疗法效率低下,这是一个严重的挑战,特别是在恶性黑色素瘤的情况下,这种癌症具有侵袭性高和相对死亡率高的特点。肿瘤微环境在黑色素瘤的进展及其对治疗的耐药性获得中的作用似乎是最近研究的主要焦点。在正常情况下,有助于机体对抗癌症的因素之一,并且在恶性转化后,适应于促进肿瘤的发展是免疫系统。多种细胞类型,即 T 和 B 淋巴细胞、巨噬细胞、树突状细胞和自然杀伤细胞以及中性粒细胞,利用包括分泌促炎分子、诱导抑制性受体表达或耗尽必需营养物质在内的多种机制,支持黑色素瘤细胞的生长和侵袭。这篇综述全面总结了肿瘤相关细胞调节的促进黑色素瘤细胞免疫逃逸的过程。所描述的机制为抗癌治疗提供了新的潜在靶点,应进一步研究以改善目前使用的治疗方法。