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Chromatin immunoprecipitation (ChIP): revisiting the efficacy of sample preparation, sonication, quantification of sheared DNA, and analysis via PCR.染色质免疫沉淀(ChIP):重新审视样品制备、超声处理、剪切 DNA 定量和 PCR 分析的效果。
PLoS One. 2011;6(10):e26015. doi: 10.1371/journal.pone.0026015. Epub 2011 Oct 25.
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A review of the epidemiology and treatment of Merkel cell carcinoma. Merkel 细胞癌的流行病学和治疗综述。
Clinics (Sao Paulo). 2011;66(10):1817-23. doi: 10.1590/s1807-59322011001000023.
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Epigenetic regulation of microRNA genes and the role of miR-34b in cell invasion and motility in human melanoma.miRNA 基因的表观遗传调控及 miR-34b 在人黑色素瘤细胞侵袭和迁移中的作用
PLoS One. 2011;6(9):e24922. doi: 10.1371/journal.pone.0024922. Epub 2011 Sep 19.
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Advances in epigenetic technology.表观遗传技术的进展。
Methods Mol Biol. 2011;791:1-10. doi: 10.1007/978-1-61779-316-5_1.
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Underestimation of Gleason score at prostate biopsy reflects sampling error in lower volume tumours.前列腺穿刺活检时低估 Gleason 评分反映了低容量肿瘤中采样误差。
BJU Int. 2012 Mar;109(5):660-4. doi: 10.1111/j.1464-410X.2011.10543.x. Epub 2011 Sep 2.
6
miR-21 and miR-155 are associated with mitotic activity and lesion depth of borderline melanocytic lesions.miR-21 和 miR-155 与交界性黑色素瘤的有丝分裂活性和病变深度有关。
Br J Cancer. 2011 Sep 27;105(7):1023-9. doi: 10.1038/bjc.2011.288. Epub 2011 Aug 23.
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A novel oncogenic role for the miRNA-506-514 cluster in initiating melanocyte transformation and promoting melanoma growth.miR-506-514 簇在启动黑素细胞转化和促进黑色素瘤生长中的新致癌作用。
Oncogene. 2012 Mar 22;31(12):1558-70. doi: 10.1038/onc.2011.345. Epub 2011 Aug 22.
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miR-30b/30d regulation of GalNAc transferases enhances invasion and immunosuppression during metastasis.miR-30b/30d 调控半乳糖胺转移酶增强转移过程中的侵袭和免疫抑制。
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FEBS Lett. 2011 Aug 4;585(15):2467-76. doi: 10.1016/j.febslet.2011.06.025. Epub 2011 Jun 26.
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Analytical aspects of microRNA in diagnostics: a review.miRNA 在诊断学中的分析方面:综述
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皮肤癌中的表观遗传生物标志物。

Epigenetic biomarkers in skin cancer.

机构信息

Department of Molecular Oncology, John Wayne Cancer Institute at Saint John's Health Center, Santa Monica, CA, USA.

出版信息

Cancer Lett. 2014 Jan 28;342(2):170-7. doi: 10.1016/j.canlet.2012.01.020. Epub 2012 Jan 27.

DOI:10.1016/j.canlet.2012.01.020
PMID:22289720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3391356/
Abstract

Epigenetic aberrations have been associated with cutaneous melanoma tumorigenesis and progression including dysregulated DNA gene promoter region methylation, histone modification, and microRNA. Several of these major epigenetic aberrations have been developed into biomarkers. Epigenetic biomarkers can be detected in tissue and in blood as circulating DNA in melanoma patients. There is strong evidence that biomarkers in cutaneous melanoma will have an important role as companions to therapeutics and overall patient management. Important progress has been made in epigenetic melanoma biomarker development and verification of clinical utility, and this review discusses some of the key current developments and existing challenges.

摘要

表观遗传异常与皮肤黑色素瘤的发生和发展有关,包括 DNA 基因启动子区域的异常甲基化、组蛋白修饰和 microRNA。其中一些主要的表观遗传异常已被开发成为生物标志物。在黑色素瘤患者的组织和血液中,如循环 DNA 中,可以检测到这些表观遗传生物标志物。有强有力的证据表明,皮肤黑色素瘤的生物标志物将作为治疗和整体患者管理的辅助手段发挥重要作用。在表观遗传黑色素瘤生物标志物的开发和临床实用性验证方面已经取得了重要进展,本综述讨论了一些当前的关键进展和存在的挑战。