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本文引用的文献

1
New Tools for Molecular Therapy of Hepatocellular Carcinoma.肝细胞癌分子治疗的新工具
Diseases. 2015 Oct 30;3(4):325-340. doi: 10.3390/diseases3040325.
2
Role of the long non-coding RNA HOTAIR in hepatocellular carcinoma.长链非编码RNA HOTAIR在肝细胞癌中的作用。
Oncol Lett. 2017 Aug;14(2):1233-1239. doi: 10.3892/ol.2017.6312. Epub 2017 Jun 6.
3
The hepatocyte-specific HNF4α/miR-122 pathway contributes to iron overload-mediated hepatic inflammation.肝细胞特异性的HNF4α/miR-122通路导致铁过载介导的肝脏炎症。
Blood. 2017 Aug 24;130(8):1041-1051. doi: 10.1182/blood-2016-12-755967. Epub 2017 Jun 27.
4
T-cell-associated immunotherapy: a promising strategy for the treatment of hepatocellular carcinoma.T细胞相关免疫疗法:一种治疗肝细胞癌的有前景的策略。
Immunotherapy. 2017 Jun;9(7):523-525. doi: 10.2217/imt-2017-0053.
5
EZH2 in Cancer Progression and Potential Application in Cancer Therapy: A Friend or Foe?EZH2在癌症进展中的作用及在癌症治疗中的潜在应用:是敌是友?
Int J Mol Sci. 2017 May 31;18(6):1172. doi: 10.3390/ijms18061172.
6
Systemic therapy for advanced hepatocellular carcinoma: an update.晚期肝细胞癌的系统治疗:最新进展
J Gastrointest Oncol. 2017 Apr;8(2):243-255. doi: 10.21037/jgo.2017.02.01.
7
Overexpression of Yes-associated protein and its association with clinicopathological features of hepatocellular carcinoma: A meta-analysis.Yes 相关蛋白过表达与肝细胞癌临床病理特征的关系:Meta 分析。
Liver Int. 2017 Nov;37(11):1675-1681. doi: 10.1111/liv.13428. Epub 2017 Apr 24.
8
Targeting Mechanotransduction at the Transcriptional Level: YAP and BRD4 Are Novel Therapeutic Targets for the Reversal of Liver Fibrosis.在转录水平靶向机械转导:YAP和BRD4是逆转肝纤维化的新型治疗靶点。
Front Pharmacol. 2016 Dec 1;7:462. doi: 10.3389/fphar.2016.00462. eCollection 2016.
9
Tremelimumab in combination with ablation in patients with advanced hepatocellular carcinoma.曲美木单抗联合消融治疗晚期肝细胞癌患者。
J Hepatol. 2017 Mar;66(3):545-551. doi: 10.1016/j.jhep.2016.10.029. Epub 2016 Nov 2.
10
Interleukin-6 enhances cancer stemness and promotes metastasis of hepatocellular carcinoma via up-regulating osteopontin expression.白细胞介素-6通过上调骨桥蛋白表达增强肝癌干细胞特性并促进肝癌转移。
Am J Cancer Res. 2016 Sep 1;6(9):1873-1889. eCollection 2016.

微环境与肿瘤细胞:肝细胞癌新分子疗法的两个靶点

Microenvironment and tumor cells: two targets for new molecular therapies of hepatocellular carcinoma.

作者信息

Amicone Laura, Marchetti Alessandra

机构信息

Department of Cellular Biotechnologies and Hematology, Sapienza University of Rome, Rome, Italy.

出版信息

Transl Gastroenterol Hepatol. 2018 May 2;3:24. doi: 10.21037/tgh.2018.04.05. eCollection 2018.

DOI:10.21037/tgh.2018.04.05
PMID:29971255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6002256/
Abstract

Hepatocellular carcinoma (HCC), is one of the most frequent human cancer and is characterized by a high mortality rate. The aggressiveness appears strictly related to the liver pathological background on which cancer develops. Inflammation and the consequent fibro/cirrhosis, derived from chronic injuries of several origins (viral, toxic and metabolic) and observable in almost all oncological patients, represents the most powerful risk factor for HCC and, at the same time, an important obstacle to the efficacy of systemic therapy. Multiple microenvironmental cues, indeed, play a pivotal role in the pathogenesis, evolution and recurrence of HCC as well as in the resistance to standard therapies observed in most of patients. The identification of altered pathways in cancer cells and of microenvironmental changes, strictly connected in pathogenic feedback loop, may permit to plan new therapeutic approaches targeting tumor cells and their permissive microenvironment, simultaneously.

摘要

肝细胞癌(HCC)是人类最常见的癌症之一,其特点是死亡率高。肿瘤的侵袭性似乎与癌症发生的肝脏病理背景密切相关。炎症以及随之而来的纤维化/肝硬化,源于多种原因(病毒、毒素和代谢)引起的慢性损伤,几乎在所有肿瘤患者中都可观察到,是HCC最强大的危险因素,同时也是全身治疗疗效的重要障碍。事实上,多种微环境信号在HCC的发病机制、进展和复发以及大多数患者对标准治疗的耐药性中都起着关键作用。识别癌细胞中改变的信号通路以及微环境变化(在致病反馈回路中紧密相连),可能有助于同时规划针对肿瘤细胞及其适宜微环境的新治疗方法。