回顾:痣会衰老吗?

IF 3.9 3区 医学 Q2 CELL BIOLOGY Pigment Cell & Melanoma Research Pub Date : 2024-02-15 DOI:10.1111/pcmr.13163
Dorothy C. Bennett
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引用次数: 0

摘要

黑素细胞痣(皮肤痣)一直被认为是体内细胞衰老的一个重要例子。然而,一项在小鼠模型中对诱导痣进行的研究报告称,痣是通过细胞相互作用而不是像衰老那样的细胞自主过程停止生长的,而且痣内细胞巢的大小分布无法用癌基因诱导衰老的随机模型来解释。此外,还有人报告说,用于识别人类痣中细胞衰老的一些分子标记也存在于黑色素瘤细胞中,而不是衰老细胞中。因此,有人质疑痣是否真的衰老,这对黑色素瘤的诊断和治疗具有潜在影响。在此,我将回顾这些领域,以及支持痣衰老的遗传学、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(平庸)痣的细胞在很大程度上是衰老的,尽管有些痣中一定含有少量非衰老细胞亚群。还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诱发的,而不是直接由癌基因诱发的。
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Review: Are moles senescent?

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.

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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
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
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