Kuzu Omer F, Noory Mohammad A, Robertson Gavin P
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.
Cancer Res. 2016 Apr 15;76(8):2063-70. doi: 10.1158/0008-5472.CAN-15-2613. Epub 2016 Apr 5.
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.
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。