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新白蛇醇通过上调PTEN抑制人胆管癌细胞的细胞生长。

Neoalbaconol inhibits cell growth of human cholangiocarcinoma cells by up-regulating PTEN.

作者信息

Zhou Guang-Yao, Pan Chen-Wei, Jin Ling-Xiang, Zheng Jian-Jian, Yi Yong-Xiang

机构信息

Department of Infectious Disease, The Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University Wenzhou 325027, China.

Wenzhou Key Laboratory of Surgery, The First Affiliated Hospital of Wenzhou Medical University Wenzhou, Zhejiang 325000, China.

出版信息

Am J Transl Res. 2016 Feb 15;8(2):496-505. eCollection 2016.

PMID:27158342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4846899/
Abstract

The recently isolated small-molecule neoalbaconol (NA) from Albatrellus confluens has been suggested to possess the ability to inhibit cell growth of many cancer cells. In this study, we investigated the role of NA in the regulation of cell apoptosis in human cholangiocarcinoma cell lines both in vitro and in vivo. Our results indicate that NA could induce cancer cell death via the AKT pathway by targeting phosphorate and tension homolog detected on chromosome 10 (PTEN) and supported the feasibility of NA being a novel chemotherapeutic treatment for human cholangiocarcinoma.

摘要

最近从融合秃牛肝菌中分离出的小分子新茯苓二醇(NA)被认为具有抑制多种癌细胞生长的能力。在本研究中,我们在体外和体内研究了NA在人胆管癌细胞系细胞凋亡调控中的作用。我们的结果表明,NA可通过靶向10号染色体上检测到的磷酸酶和张力同源物(PTEN),经由AKT途径诱导癌细胞死亡,并支持了NA作为人胆管癌新型化疗药物的可行性。

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Am J Transl Res. 2016 Feb 15;8(2):496-505. eCollection 2016.
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本文引用的文献

1
The role of targeting kinase activity by natural products in cancer chemoprevention and chemotherapy (Review).天然产物靶向激酶活性在癌症化学预防和化疗中的作用(综述)
Oncol Rep. 2015 Aug;34(2):547-54. doi: 10.3892/or.2015.4029. Epub 2015 Jun 4.
2
Pathogenesis of cholangiocarcinoma: From genetics to signalling pathways.胆管癌的发病机制:从遗传学到信号通路
Best Pract Res Clin Gastroenterol. 2015 Apr;29(2):233-44. doi: 10.1016/j.bpg.2015.02.002. Epub 2015 Feb 17.
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Epidemiology of cholangiocarcinoma.胆管癌的流行病学
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MicroRNA-302a Suppresses Tumor Cell Proliferation by Inhibiting AKT in Prostate Cancer.微小RNA-302a通过抑制前列腺癌中的AKT来抑制肿瘤细胞增殖。
PLoS One. 2015 Apr 29;10(4):e0124410. doi: 10.1371/journal.pone.0124410. eCollection 2015.
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Neoalbaconol induces cell death through necroptosis by regulating RIPK-dependent autocrine TNFα and ROS production.新白腐醇通过调节RIPK依赖性自分泌TNFα和ROS生成,经由坏死性凋亡诱导细胞死亡。
Oncotarget. 2015 Feb 10;6(4):1995-2008. doi: 10.18632/oncotarget.3038.
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Mutational landscape of intrahepatic cholangiocarcinoma.肝内胆管癌的突变全景图。
Nat Commun. 2014 Dec 15;5:5696. doi: 10.1038/ncomms6696.
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Palliation: Hilar cholangiocarcinoma.姑息治疗:肝门部胆管癌。
World J Hepatol. 2014 Aug 27;6(8):559-69. doi: 10.4254/wjh.v6.i8.559.
8
CRISPR-mediated direct mutation of cancer genes in the mouse liver.CRISPR介导的小鼠肝脏中癌症基因的直接突变。
Nature. 2014 Oct 16;514(7522):380-4. doi: 10.1038/nature13589. Epub 2014 Aug 6.
9
Hilar cholangiocarcinoma: diagnosis, treatment options, and management.肝门部胆管癌:诊断、治疗选择及管理
Hepatobiliary Surg Nutr. 2014 Feb;3(1):18-34. doi: 10.3978/j.issn.2304-3881.2014.02.05.
10
Neoalbaconol induces energy depletion and multiple cell death in cancer cells by targeting PDK1-PI3-K/Akt signaling pathway.新姜酚通过靶向 PDK1-PI3-K/Akt 信号通路诱导癌细胞能量耗竭和多种细胞死亡。
Cell Death Dis. 2013 Sep 19;4(9):e804. doi: 10.1038/cddis.2013.324.