Peter Hersey, Hsin-Yi Tseng, Sara Alavi, Jessamy Tiffen
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引用次数: 0
Abstract
Marked differences in survival from melanoma are noted between men and women that cannot be accounted for by behavioral differences. We and others have provided evidence that this difference may be due to increased expression of immune-related genes from the second X chromosome because of failure of X inactivation. In the present review, we have examined evidence for the contrary view that survival differences are due to weaker immune responses in males. One reason for this may be the loss of Y chromosomes (LOY), particularly in older males. The genes involved may have direct roles in immune responses or be noncoding RNAs that regulate both sex and autosomal genes involved in immune responses or tumor growth. Loss of the KDM6C and KDM5D demethylases appeared to common genes involved. The second factor appears to be the activation of androgen receptors (AR) on melanoma cells that increase their invasiveness and growth. Induction of T-cell exhaustion by AR that limits immune responses against melanoma appeared a common finding. The development of treatments to overcome effects related to gene loss on Y poses challenges, but several avenues related to AR signaling appear worthy of further study in the treatment of metastatic disease.
男性和女性在黑色素瘤的存活率上存在明显差异,而这种差异无法用行为差异来解释。我们和其他人提供的证据表明,这种差异可能是由于 X 失活导致第二 X 染色体免疫相关基因的表达增加所致。在本综述中,我们研究了支持相反观点的证据,即生存差异是由于雄性的免疫反应较弱。其中一个原因可能是 Y 染色体缺失(LOY),尤其是在老年男性中。所涉及的基因可能在免疫反应中起直接作用,也可能是非编码 RNA,这些 RNA 既能调控性别基因,也能调控参与免疫反应或肿瘤生长的常染色体基因。KDM6C 和 KDM5D 去甲基化酶的缺失似乎是常见的相关基因。第二个因素似乎是黑色素瘤细胞上的雄激素受体(AR)被激活,从而增加了其侵袭性和生长。AR诱导T细胞衰竭,限制了针对黑色素瘤的免疫反应,这似乎是一个共同的发现。开发治疗方法以克服与Y基因缺失有关的影响是一项挑战,但在治疗转移性疾病方面,与AR信号有关的几种途径似乎值得进一步研究。
期刊介绍:
Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords
Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders