Molecular & Clinical Sciences Research Institute, St George's University of London, London, UK.
Pigment Cell Melanoma Res. 2024 May;37(3):391-402. doi: 10.1111/pcmr.13163. Epub 2024 Feb 15.
Melanocytic nevi (skin moles) have been regarded as a valuable example of cell senescence occurring in vivo. However, a study of induced nevi in a mouse model reported that the nevi were arrested by cell interactions rather than a cell-autonomous process like senescence, and that size distributions of cell nests within nevi could not be accounted for by a stochastic model of oncogene-induced senescence. Moreover, others reported that some molecular markers used to identify cell senescence in human nevi are also found in melanoma cells-not senescent. It has thus been questioned whether nevi really are senescent, with potential implications for melanoma diagnosis and therapy. Here I review these areas, along with the genetic, biological, and molecular evidence supporting senescence in nevi. In conclusion, there is strong evidence that cells of acquired human benign (banal) nevi are very largely senescent, though some must contain a minor non-senescent cell subpopulation. There is also persuasive evidence that this senescence is primarily induced by dysfunctional telomeres rather than directly oncogene-induced.
黑素细胞痣(皮肤痣)一直被认为是体内细胞衰老的一个有价值的例子。然而,一项在小鼠模型中诱导痣的研究报告称,痣是被细胞相互作用而非像衰老那样的细胞自主过程所阻止的,并且痣内细胞巢的大小分布不能用致癌基因诱导衰老的随机模型来解释。此外,其他人报告说,用于鉴定人类痣中细胞衰老的一些分子标记物也存在于黑色素瘤细胞中——并非衰老。因此,人们质疑痣是否真的衰老了,这对黑色素瘤的诊断和治疗有潜在的影响。在这里,我回顾了这些领域,以及支持痣中衰老的遗传、生物学和分子证据。总之,有强有力的证据表明,获得性人类良性(普通)痣的细胞在很大程度上是衰老的,尽管其中一些必须包含一小部分非衰老细胞亚群。也有令人信服的证据表明,这种衰老主要是由功能失调的端粒引起的,而不是直接由致癌基因引起的。