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针对癌症治疗的表观遗传学靶点。

Targeting epigenetics for cancer therapy.

机构信息

Research Center for Epigenome Regulation, School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.

出版信息

Arch Pharm Res. 2019 Feb;42(2):159-170. doi: 10.1007/s12272-019-01126-z. Epub 2019 Feb 26.

Abstract

Cancer can be identified as a chaotic cell state, which breaks the rules that govern growth and reproduction, with main characteristics such as uncontrolled division, invading other tissues, usurping resources, and eventually killing its host. It was once believed that cancer is caused by a progressive series of genetic aberrations, and certain mutations of genes, including oncogenes and tumor suppressor genes, have been identified as the cause of cancer. However, piling evidence suggests that epigenetic modifications working in concert with genetic mechanisms to regulate transcriptional activity are dysregulated in many diseases, including cancer. Cancer epigenetics explain a wide range of heritable changes in gene expression, which do not come from any alteration in DNA sequences. Aberrant DNA methylation, histone modifications, and expression of long non-coding RNAs (lncRNAs) are key epigenetic mechanisms associated with tumor initiation, cancer progression, and metastasis. Within the past decade, cancer epigenetics have enabled us to develop novel biomarkers and therapeutic target for many types of cancers. In this review, we will summarize the major epigenetic changes involved in cancer biology along with clinical and preclinical results developed as novel cancer therapeutics.

摘要

癌症可以被识别为一种混乱的细胞状态,它打破了控制生长和繁殖的规则,主要特征包括不受控制的分裂、侵犯其他组织、篡夺资源,最终杀死宿主。曾经认为癌症是由一系列渐进的遗传异常引起的,包括癌基因和肿瘤抑制基因在内的某些基因突变已被确定为癌症的原因。然而,越来越多的证据表明,表观遗传修饰与遗传机制一起协同调节转录活性,在许多疾病中失调,包括癌症。癌症表观遗传学解释了广泛的基因表达可遗传变化,这些变化不是来自 DNA 序列的任何改变。异常的 DNA 甲基化、组蛋白修饰和长非编码 RNA(lncRNA)的表达是与肿瘤起始、癌症进展和转移相关的关键表观遗传机制。在过去的十年中,癌症表观遗传学使我们能够为许多类型的癌症开发新的生物标志物和治疗靶点。在这篇综述中,我们将总结涉及癌症生物学的主要表观遗传变化,以及作为新型癌症治疗方法开发的临床前和临床结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193b/6399185/57822af73789/12272_2019_1126_Fig1_HTML.jpg

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