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本文引用的文献

1
Squalene epoxidase is a bona fide oncogene by amplification with clinical relevance in breast cancer.角鲨烯环氧酶通过在乳腺癌中扩增而成为具有临床相关性的真正癌基因。
Sci Rep. 2016 Jan 18;6:19435. doi: 10.1038/srep19435.
2
Targeting cholesterol with β-cyclodextrin sensitizes cancer cells for apoptosis.用β-环糊精靶向胆固醇可使癌细胞对凋亡敏感。
FEBS Lett. 2015 Dec 21;589(24 Pt B):4097-105. doi: 10.1016/j.febslet.2015.11.009. Epub 2015 Nov 25.
3
Neuregulin-activated ERBB4 induces the SREBP-2 cholesterol biosynthetic pathway and increases low-density lipoprotein uptake.神经调节蛋白激活的ERBB4诱导SREBP-2胆固醇生物合成途径并增加低密度脂蛋白摄取。
Sci Signal. 2015 Nov 3;8(401):ra111. doi: 10.1126/scisignal.aac5124.
4
Endogenous Sterol Metabolites Regulate Growth of EGFR/KRAS-Dependent Tumors via LXR.内源性甾醇代谢产物通过肝X受体调节EGFR/KRAS依赖性肿瘤的生长。
Cell Rep. 2015 Sep 22;12(11):1927-38. doi: 10.1016/j.celrep.2015.08.023. Epub 2015 Sep 3.
5
Squalene epoxidase (SQLE) promotes the growth and migration of the hepatocellular carcinoma cells.角鲨烯环氧酶(SQLE)促进肝癌细胞的生长和迁移。
Tumour Biol. 2015 Aug;36(8):6173-9. doi: 10.1007/s13277-015-3301-x. Epub 2015 Mar 19.
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The cholesterol biosynthesis enzyme oxidosqualene cyclase is a new target to impair tumour angiogenesis and metastasis dissemination.胆固醇生物合成酶氧化角鲨烯环化酶是破坏肿瘤血管生成和转移扩散的新靶点。
Sci Rep. 2015 Mar 12;5:9054. doi: 10.1038/srep09054.
7
Elevated levels of StAR-related lipid transfer protein 3 alter cholesterol balance and adhesiveness of breast cancer cells: potential mechanisms contributing to progression of HER2-positive breast cancers.与类固醇生成急性调节蛋白相关的脂质转运蛋白3水平升高会改变乳腺癌细胞的胆固醇平衡和黏附性:这是导致HER2阳性乳腺癌进展的潜在机制。
Am J Pathol. 2015 Apr;185(4):987-1000. doi: 10.1016/j.ajpath.2014.12.018. Epub 2015 Feb 12.
8
Role of cholesterol in SNARE-mediated trafficking on intracellular membranes.胆固醇在SNARE介导的细胞内膜运输中的作用。
J Cell Sci. 2015 Mar 15;128(6):1071-81. doi: 10.1242/jcs.164459. Epub 2015 Feb 4.
9
Association between cholesterol intake and pancreatic cancer risk: evidence from a meta-analysis.胆固醇摄入量与胰腺癌风险之间的关联:一项荟萃分析的证据。
Sci Rep. 2015 Feb 4;5:8243. doi: 10.1038/srep08243.
10
Statins do not protect against cancer: quite the opposite.他汀类药物不能预防癌症:恰恰相反。
J Clin Oncol. 2015 Mar 1;33(7):810-1. doi: 10.1200/JCO.2014.58.9564. Epub 2015 Jan 20.

胆固醇在癌症中的作用。

The Role of Cholesterol in Cancer.

作者信息

Kuzu Omer F, Noory Mohammad A, Robertson Gavin P

机构信息

Department of Pharmacology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania.

Department of Pharmacology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. Department of Pathology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. Department of Dermatology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. Department of Surgery, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. Penn State Hershey Melanoma Center, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. Penn State Melanoma Therapeutics Program, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. Penn State Hershey Cancer Institute, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania. The Foreman Foundation for Melanoma Research, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania.

出版信息

Cancer Res. 2016 Apr 15;76(8):2063-70. doi: 10.1158/0008-5472.CAN-15-2613. Epub 2016 Apr 5.

DOI:10.1158/0008-5472.CAN-15-2613
PMID:27197250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5813477/
Abstract

The roles played by cholesterol in cancer development and the potential of therapeutically targeting cholesterol homeostasis is a controversial area in the cancer community. Several epidemiologic studies report an association between cancer and serum cholesterol levels or statin use, while others suggest that there is not one. Furthermore, the Cancer Genome Atlas (TCGA) project using next-generation sequencing has profiled the mutational status and expression levels of all the genes in diverse cancers, including those involved in cholesterol metabolism, providing correlative support for a role of the cholesterol pathway in cancer development. Finally, preclinical studies tend to more consistently support the role of cholesterol in cancer, with several demonstrating that cholesterol homeostasis genes can modulate development. Because of space limitations, this review provides selected examples of the epidemiologic, TCGA, and preclinical data, focusing on alterations in cholesterol homeostasis and its consequent effect on patient survival. In melanoma, this focused analysis demonstrated that enhanced expression of cholesterol synthesis genes was associated with decreased patient survival. Collectively, the studies in melanoma and other cancer types suggested a potential role of disrupted cholesterol homeostasis in cancer development but additional studies are needed to link population-based epidemiological data, the TCGA database results, and preclinical mechanistic evidence to concretely resolve this controversy. Cancer Res; 76(8); 2063-70. ©2016 AACR.

摘要

胆固醇在癌症发展中所起的作用以及靶向胆固醇稳态进行治疗的潜力,是癌症领域中一个存在争议的话题。多项流行病学研究报告了癌症与血清胆固醇水平或他汀类药物使用之间的关联,而其他研究则表明不存在这种关联。此外,癌症基因组图谱(TCGA)项目利用新一代测序技术,对多种癌症中所有基因的突变状态和表达水平进行了分析,包括那些参与胆固醇代谢的基因,为胆固醇途径在癌症发展中的作用提供了相关支持。最后,临床前研究往往更一致地支持胆固醇在癌症中的作用,有几项研究表明胆固醇稳态基因可以调节癌症发展。由于篇幅限制,本综述提供了流行病学、TCGA和临床前数据的部分示例,重点关注胆固醇稳态的改变及其对患者生存的影响。在黑色素瘤中,这种重点分析表明胆固醇合成基因的表达增强与患者生存率降低有关。总体而言,黑色素瘤和其他癌症类型的研究表明,胆固醇稳态破坏在癌症发展中可能起作用,但需要更多研究将基于人群的流行病学数据、TCGA数据库结果和临床前机制证据联系起来,以具体解决这一争议。《癌症研究》;76(8);2063 - 70。©2016美国癌症研究协会。