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Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin.人类皮肤中 p53 免疫阳性斑块中与癌症相关的基因突变的亚克隆进化。
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本文引用的文献

1
Subclonal Evolution of Cancer-Related Gene Mutations in p53 Immunopositive Patches in Human Skin.人类皮肤中 p53 免疫阳性斑块中与癌症相关的基因突变的亚克隆进化。
J Invest Dermatol. 2018 Jan;138(1):189-198. doi: 10.1016/j.jid.2017.07.844. Epub 2017 Aug 24.
2
Tissue-specific mutation accumulation in human adult stem cells during life.人类成体干细胞在生命过程中的组织特异性突变积累。
Nature. 2016 Oct 13;538(7624):260-264. doi: 10.1038/nature19768. Epub 2016 Oct 3.
3
Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults.携带 AML 相关突变的克隆性造血在健康成年人中普遍存在。
Nat Commun. 2016 Aug 22;7:12484. doi: 10.1038/ncomms12484.
4
Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin.肿瘤进化。正常人类皮肤中体细胞突变的高负担和普遍正向选择。
Science. 2015 May 22;348(6237):880-6. doi: 10.1126/science.aaa6806.
5
Age-related mutations associated with clonal hematopoietic expansion and malignancies.与克隆性造血扩张和恶性肿瘤相关的年龄相关突变。
Nat Med. 2014 Dec;20(12):1472-8. doi: 10.1038/nm.3733. Epub 2014 Oct 19.
6
Temporal dissection of tumorigenesis in primary cancers.原发性癌症中肿瘤发生的时程剖析。
Cancer Discov. 2011 Jul;1(2):137-43. doi: 10.1158/2159-8290.CD-11-0028. Epub 2011 Jun 29.
7
Protection against UVR involves MC1R-mediated non-pigmentary and pigmentary mechanisms in vivo.UVR 的防护涉及 MC1R 介导的体内非色素和色素机制。
J Invest Dermatol. 2010 Jul;130(7):1904-13. doi: 10.1038/jid.2010.48. Epub 2010 Mar 18.
8
Relationship between UV-induced mutant p53 patches and skin tumours, analysed by mutation spectra and by induction kinetics in various DNA-repair-deficient mice.通过突变谱以及在各种DNA修复缺陷小鼠中的诱导动力学分析紫外线诱导的突变型p53斑块与皮肤肿瘤之间的关系。
Carcinogenesis. 2005 Dec;26(12):2123-30. doi: 10.1093/carcin/bgi198. Epub 2005 Jul 28.
9
Frequent clones of p53-mutated keratinocytes in normal human skin.正常人皮肤中p53突变角质形成细胞的频繁克隆。
Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):14025-9. doi: 10.1073/pnas.93.24.14025.

日光性皮肤损伤中突变热点的出现和演变。

Emergence and Evolution of Mutational Hotspots in Sun-Damaged Skin.

机构信息

Department of Dermatology, University of California, San Francisco, California, USA; Veterans Affairs Medical Center, San Francisco, California, USA.

Department of Dermatology, University of California, San Francisco, California, USA.

出版信息

J Invest Dermatol. 2018 Jan;138(1):16-17. doi: 10.1016/j.jid.2017.09.007.

DOI:10.1016/j.jid.2017.09.007
PMID:29273145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6053279/
Abstract

In this issue, Albibas et al. investigate the mutational nature of p53-immunopositive patches, commonly observed in sun-damaged skin. p53-immunopositive patches have long been suspected to be lineal precursors to actinic keratoses and cutaneous squamous cell carcinomas. However, the mutations actually giving rise to p53-immunopositive patches, and their relationship to skin cancer, have never been defined. The considerable clinical and economic costs of monitoring and treating sun-damaged skin demand we better understand the evolution of these common premalignancies.

摘要

在本期杂志中,Albibas 等人研究了 p53 免疫阳性斑块的突变性质,这些斑块在日光损伤的皮肤中很常见。p53 免疫阳性斑块长期以来一直被怀疑是光化性角化病和皮肤鳞状细胞癌的线性前体。然而,实际上导致 p53 免疫阳性斑块的突变及其与皮肤癌的关系从未被定义过。监测和治疗日光损伤皮肤的巨大临床和经济成本要求我们更好地了解这些常见癌前病变的演变。