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本文引用的文献

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Copy number variations of are prognostic biomarkers for hepatocellular carcinoma.的拷贝数变异是肝细胞癌的预后生物标志物。 (原文中“of”后面缺少具体内容)
Transl Cancer Res. 2020 Feb;9(2):698-706. doi: 10.21037/tcr.2019.11.52.
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The mechanisms of sorafenib resistance in hepatocellular carcinoma: theoretical basis and therapeutic aspects.索拉非尼耐药在肝细胞癌中的机制:理论基础和治疗方面。
Signal Transduct Target Ther. 2020 Jun 10;5(1):87. doi: 10.1038/s41392-020-0187-x.
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Dedifferentiation of hepatocellular carcinoma: molecular mechanisms and therapeutic implications.肝细胞癌的去分化:分子机制及治疗意义
Am J Transl Res. 2020 May 15;12(5):2099-2109. eCollection 2020.
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Clinical significance of combined circulating TERT promoter mutations and miR-122 expression for screening HBV-related hepatocellular carcinoma.联合检测循环端粒酶逆转录酶启动子突变和 miR-122 表达对筛查乙型肝炎病毒相关肝细胞癌的临床意义。
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Identification of noninvasive diagnostic biomarkers for hepatocellular carcinoma by urinary proteomics.尿蛋白质组学鉴定肝细胞癌的非侵入性诊断生物标志物。
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Implications of driver genes associated with a high tumor mutation burden identified using next-generation sequencing on immunotherapy in hepatocellular carcinoma.利用下一代测序技术鉴定出的与高肿瘤突变负担相关的驱动基因对肝细胞癌免疫治疗的影响
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Development and validation of a 14-gene signature for prognosis prediction in hepatocellular carcinoma.开发并验证用于预测肝细胞癌预后的 14 基因标志物。
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Single-cell analysis reveals different age-related somatic mutation profiles between stem and differentiated cells in human liver.单细胞分析揭示了人类肝脏中的干细胞和分化细胞之间与年龄相关的不同体细胞突变特征。
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CRISPR/Cas9 genome-wide screening identifies KEAP1 as a sorafenib, lenvatinib, and regorafenib sensitivity gene in hepatocellular carcinoma.CRISPR/Cas9全基因组筛选确定KEAP1为肝细胞癌中索拉非尼、乐伐替尼和瑞戈非尼的敏感性基因。
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Multiple novel hepatocellular carcinoma signature genes are commonly controlled by the master pluripotency factor OCT4.多个新型肝癌特征基因通常受多能性主调控因子 OCT4 控制。
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肝癌的基因组图谱

Genomic Landscape of HCC.

作者信息

Nia Adeniji, Dhanasekaran Renumathy

机构信息

Stanford School of Medicine, Stanford, CA.

Division of Gastroenterology and Hepatology, Stanford, CA.

出版信息

Curr Hepatol Rep. 2020 Dec;19(4):448-461. doi: 10.1007/s11901-020-00553-7. Epub 2020 Nov 10.

DOI:10.1007/s11901-020-00553-7
PMID:33816052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8015384/
Abstract

INTRODUCTION

Hepatocellular carcinoma (HCC) is a leading cause of cancer related mortality in the world and it has limited treatment options. Understanding the molecular drivers of HCC is important to develop novel biomarkers and therapeutics.

PURPOSE OF REVIEW

HCC arises in a complex background of chronic hepatitis, fibrosis and liver regeneration which lead to genomic changes. Here, we summarize studies that have expanded our understanding of the molecular landscape of HCC.

RECENT FINDINGS

Recent technological advances in next generation sequencing (NGS) have elucidated specific genetic and molecular programs involved in hepatocarcinogenesis. We summarize the major somatic mutations and epigenetic changes have been identified in NGS-based studies. We also describe promising molecular therapies and immunotherapies which target specific genetic and epigenetic molecular events.

SUMMARY

The genomic landscape of HCC is incredibly complex and heterogeneous. Promising new developments are helping us decipher the molecular drivers of HCC and leading to new therapies.

摘要

引言

肝细胞癌(HCC)是全球癌症相关死亡的主要原因之一,其治疗选择有限。了解HCC的分子驱动因素对于开发新型生物标志物和治疗方法至关重要。

综述目的

HCC发生于慢性肝炎、纤维化和肝再生的复杂背景中,这些会导致基因组变化。在此,我们总结了一些研究,这些研究扩展了我们对HCC分子格局的理解。

最新发现

下一代测序(NGS)技术的最新进展阐明了参与肝癌发生的特定基因和分子程序。我们总结了基于NGS的研究中已确定的主要体细胞突变和表观遗传变化。我们还描述了针对特定基因和表观遗传分子事件的有前景的分子疗法和免疫疗法。

总结

HCC的基因组格局极其复杂且具有异质性。有前景的新进展正在帮助我们解读HCC的分子驱动因素,并带来新的治疗方法。