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本文引用的文献

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SAHA and cisplatin sensitize gastric cancer cells to doxorubicin by induction of DNA damage, apoptosis and perturbation of AMPK-mTOR signalling.SAHA 和顺铂通过诱导 DNA 损伤、细胞凋亡和干扰 AMPK-mTOR 信号通路使胃癌细胞对阿霉素敏感。
Exp Cell Res. 2018 Sep 15;370(2):283-291. doi: 10.1016/j.yexcr.2018.06.029. Epub 2018 Jun 28.
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SETD2 indicates favourable prognosis in gastric cancer and suppresses cancer cell proliferation, migration, and invasion.SETD2 表明胃癌预后良好,并抑制癌细胞增殖、迁移和侵袭。
Biochem Biophys Res Commun. 2018 Apr 6;498(3):579-585. doi: 10.1016/j.bbrc.2018.03.022. Epub 2018 Mar 9.
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Phase I combination study of the PARP inhibitor veliparib plus carboplatin and gemcitabine in patients with advanced ovarian cancer and other solid malignancies.晚期卵巢癌和其他实体瘤患者中 PARP 抑制剂维利帕尼联合卡铂和吉西他滨的 I 期联合研究。
Gynecol Oncol. 2018 Mar;148(3):507-514. doi: 10.1016/j.ygyno.2017.12.029. Epub 2018 Jan 17.
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LncRNA Structural Characteristics in Epigenetic Regulation.长链非编码 RNA 的结构特征与表观遗传调控。
Int J Mol Sci. 2017 Dec 8;18(12):2659. doi: 10.3390/ijms18122659.
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Co-regulation of transcription by BRG1 and BRM, two mutually exclusive SWI/SNF ATPase subunits.BRG1 和 BRM 通过相互排斥的 SWI/SNF ATPase 亚基共同调节转录。
Epigenetics Chromatin. 2017 Dec 22;10(1):62. doi: 10.1186/s13072-017-0167-8.
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Integration of Next-Generation Sequencing to Treat Acute Lymphoblastic Leukemia with Targetable Lesions: The St. Jude Children's Research Hospital Approach.整合下一代测序技术治疗伴有可靶向病变的急性淋巴细胞白血病:圣犹大儿童研究医院的方法。
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Stable transgenerational epigenetic inheritance requires a DNA methylation-sensing circuit.稳定的跨代表观遗传遗传需要一个 DNA 甲基化感应回路。
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The helicase domain of Polθ counteracts RPA to promote alt-NHEJ.Polθ的解旋酶结构域可对抗RPA以促进替代性非同源末端连接。
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Targeting glioma stem cells through combined BMI1 and EZH2 inhibition.通过联合抑制BMI1和EZH2靶向胶质瘤干细胞
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利用精准医学中的合成致死作用靶向表观遗传学。

Targeting epigenetics using synthetic lethality in precision medicine.

机构信息

Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117597, Singapore.

National University Health System (NUHS), Singapore, 119228, Singapore.

出版信息

Cell Mol Life Sci. 2018 Sep;75(18):3381-3392. doi: 10.1007/s00018-018-2866-0. Epub 2018 Jul 12.

DOI:10.1007/s00018-018-2866-0
PMID:30003270
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11105276/
Abstract

Technological breakthroughs in genomics have had a significant impact on clinical therapy for human diseases, allowing us to use patient genetic differences to guide medical care. The "synthetic lethal approach" leverages on cancer-specific genetic rewiring to deliver a therapeutic regimen that preferentially targets malignant cells while sparing normal cells. The utility of this system is evident in several recent studies, particularly in poor prognosis cancers with loss-of-function mutations that become "treatable" when two otherwise discrete and unrelated genes are targeted simultaneously. This review focuses on the chemotherapeutic targeting of epigenetic alterations in cancer cells and consolidates a network that outlines the interplay between epigenetic and genetic regulators in DNA damage repair. This network consists of numerous synergistically acting relationships that are druggable, even in recalcitrant triple-negative breast cancer. This collective knowledge points to the dawn of a new era of personalized medicine.

摘要

基因组学的技术突破对人类疾病的临床治疗产生了重大影响,使我们能够利用患者的基因差异来指导医疗护理。“合成致死方法”利用肿瘤特异性基因重排,提供一种治疗方案,优先靶向恶性细胞,同时保护正常细胞。该系统在几项最近的研究中得到了证实,特别是在预后不良的癌症中,当同时靶向两个原本离散且不相关的基因时,具有功能丧失突变的癌症变得“可治疗”。本综述重点介绍了癌细胞中表观遗传改变的化疗靶向,并整合了一个网络,概述了表观遗传和遗传调节剂在 DNA 损伤修复中的相互作用。该网络由许多协同作用的关系组成,即使在难治性三阴性乳腺癌中也是可用药的。这些集体知识表明个性化医疗的新时代即将到来。