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CDKN2A 和 CDKN2B 缺失导致黑色素瘤中心体过度复制。

Loss of Both CDKN2A and CDKN2B Allows for Centrosome Overduplication in Melanoma.

机构信息

Cell Biology Research Centre, Molecular and Clinical Sciences Research Institute, St. George's, University of London, Cranmer Terrace, London, United Kingdom.

Centre for Biomedical Sciences, Department of Biological Sciences, School of Life Sciences and the Environment, Royal Holloway University of London, Egham, United Kingdom.

出版信息

J Invest Dermatol. 2020 Sep;140(9):1837-1846.e1. doi: 10.1016/j.jid.2020.01.024. Epub 2020 Feb 15.

Abstract

Centrosomes duplicate only once in coordination with the DNA replication cycle and have an important role in segregating genetic material. In contrast, most cancer cells have centrosome aberrations, including supernumerary centrosomes, and this correlates with aneuploidy and genetic instability. The tumor suppressors p16 (CDKN2A) and p15 (CDKN2B) (encoded by the familial melanoma CDKN2 locus) inhibit CDK4/6 activity and have important roles in cellular senescence. p16 is also associated with suppressing centrosomal aberrations in breast cancer; however, the role of p15 in centrosome amplification is unknown. Here, we investigated the relationship between p15 and p16 expression, centrosome number abnormalities, and melanoma progression in cell lines derived from various stages of melanoma progression. We found that normal human melanocyte lines did not exhibit centrosome number abnormalities, whereas those from later stages of melanoma did. Additionally, under conditions of S-phase block, p15 and p16 status determined whether centrosome overduplication would occur. Indeed, removal of p15 from p16-negative cell lines derived from various stages of melanoma progression changed cells that previously would not overduplicate their centrosomes into cells that did. Although this study used cell lines in vitro, it suggests that, during clinical melanoma progression, sequential loss of p15 and p16 provides conditions for centrosome duplication to become deregulated with consequences for genome instability.

摘要

中心体仅在与 DNA 复制周期协调一致的情况下复制一次,在分离遗传物质方面具有重要作用。相比之下,大多数癌细胞存在中心体异常,包括多余的中心体,这与非整倍体和遗传不稳定性相关。肿瘤抑制因子 p16(CDKN2A)和 p15(CDKN2B)(由家族性黑色素瘤 CDKN2 基因座编码)抑制 CDK4/6 的活性,在细胞衰老中具有重要作用。p16 还与抑制乳腺癌中的中心体异常有关;然而,p15 在中心体扩增中的作用尚不清楚。在这里,我们研究了 p15 和 p16 表达、中心体数量异常与黑色素瘤进展细胞系之间的关系。我们发现,正常的人黑色素细胞系没有出现中心体数量异常,而那些来自黑色素瘤后期的细胞系则有。此外,在 S 期阻断的情况下,p15 和 p16 的状态决定了中心体是否会过度复制。事实上,从黑色素瘤进展的不同阶段去除 p16 阴性细胞系中的 p15,将先前不会过度复制其中心体的细胞转变为会过度复制中心体的细胞。尽管这项研究使用了体外细胞系,但它表明,在临床黑色素瘤进展过程中,p15 和 p16 的连续缺失为中心体复制失去调控提供了条件,从而导致基因组不稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9256/7435684/a51bd702a2f6/gr1.jpg

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