The Role of Cholesterol in Cancer

被引:492
作者
Kuzu, Omer F. [1 ]
Noory, Mohammad A. [1 ]
Robertson, Gavin P. [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Penn State Univ, Coll Med, Dept Pharmacol, 500 Univ Dr, Hershey, PA 17033 USA
[2] Penn State Univ, Coll Med, Dept Pathol, Hershey, PA 17033 USA
[3] Penn State Univ, Coll Med, Dept Dermatol, Hershey, PA 17033 USA
[4] Penn State Univ, Coll Med, Dept Surg, Hershey, PA 17033 USA
[5] Penn State Univ, Coll Med, Penn State Hershey Melanoma Ctr, Hershey, PA 17033 USA
[6] Penn State Univ, Coll Med, Penn State Melanoma Therapeut Program, Hershey, PA 17033 USA
[7] Penn State Univ, Coll Med, Penn State Hershey Canc Inst, Hershey, PA 17033 USA
[8] Penn State Univ, Coll Med, Foreman Fdn Melanoma Res, Hershey, PA 17033 USA
基金
美国国家卫生研究院;
关键词
PROSTATE-CANCER; SQUALENE EPOXIDASE; COLORECTAL-CANCER; CELL-DEATH; STATIN USE; PATHWAY; METABOLISM; INHIBITION; PROMOTES; RISK;
D O I
10.1158/0008-5472.CAN-15-2613
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 homeo-stasis 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. (C) 2016 AACR.
引用
收藏
页码:2063 / 2070
页数:8
相关论文
共 70 条
  • [11] The role of cholesterol metabolism and cholesterol transport in carcinogenesis: a review of scientific findings, relevant to future cancer therapeutics
    Cruz, Pedro M. R.
    Mo, Huanbiao
    McConathy, Walter J.
    Sabnis, Nirupama
    Lacko, Andras G.
    [J]. FRONTIERS IN PHARMACOLOGY, 2013, 4
  • [12] Annexin A6-induced alterations in cholesterol transport and caveolin export from the golgi complex
    Cubells, Laia
    de Muga, Sandra Vila
    Tebar, Francesc
    Wood, Peta
    Evans, Rachael
    Ingelmo-Torres, Mercedes
    Calvo, Maria
    Gaus, Katharina
    Pol, Albert
    Grewal, Thomas
    Enrich, Carlos
    [J]. TRAFFIC, 2007, 8 (11) : 1568 - 1589
  • [13] Oxysterol receptors, AKT and prostate cancer
    Dufour, Julie
    Viennois, Emilie
    De Boussac, Hugues
    Baron, Silvere
    Lobaccaro, Jean-Marc
    [J]. CURRENT OPINION IN PHARMACOLOGY, 2012, 12 (06) : 724 - 728
  • [14] Role of cholesterol in SNARE-mediated trafficking on intracellular membranes
    Enrich, Carlos
    Rentero, Carles
    Hierro, Aitor
    Grewal, Thomas
    [J]. JOURNAL OF CELL SCIENCE, 2015, 128 (06) : 1071 - 1081
  • [15] Novel actions of estrogen to promote proliferation: Integration of cytoplasmic and nuclear pathways
    Fox, Emily M.
    Andrade, Josefa
    Shupnik, Margaret A.
    [J]. STEROIDS, 2009, 74 (07) : 622 - 627
  • [16] Mutant p53 Disrupts Mammary Tissue Architecture via the Mevalonate Pathway
    Freed-Pastor, William A.
    Mizuno, Hideaki
    Zhao, Xi
    Langerod, Anita
    Moon, Sung-Hwan
    Rodriguez-Barrueco, Ruth
    Barsotti, Anthony
    Chicas, Agustin
    Li, Wencheng
    Polotskaia, Alla
    Bissell, Mina J.
    Osborne, Timothy F.
    Tian, Bin
    Lowe, Scott W.
    Silva, Jose M.
    Borresen-Dale, Anne-Lise
    Levine, Arnold J.
    Bargonetti, Jill
    Prives, Carol
    [J]. CELL, 2012, 148 (1-2) : 244 - 258
  • [17] Endogenous Sterol Metabolites Regulate Growth of EGFR/KRAS-Dependent Tumors via LXR
    Gabitova, Linara
    Restifo, Diana
    Gorin, Andrey
    Manocha, Kunal
    Handorf, Elizabeth
    Yang, Dong-Hua
    Cai, Kathy Q.
    Klein-Szanto, Andres J.
    Cunningham, David
    Kratz, Lisa E.
    Herman, Gail E.
    Golemis, Erica A.
    Astsaturov, Igor
    [J]. CELL REPORTS, 2015, 12 (11): : 1927 - 1938
  • [18] Mevalonate Metabolism Regulates Basal Breast Cancer Stem Cells and Is a Potential Therapeutic Target
    Ginestier, Christophe
    Monville, Florence
    Wicinski, Julien
    Cabaud, Olivier
    Cervera, Nathalie
    Josselin, Emmanuelle
    Finetti, Pascal
    Guille, Arnaud
    Larderet, Gaelle
    Viens, Patrice
    Sebti, Said
    Bertucci, Francois
    Birnbaum, Daniel
    Charafe-Jauffret, Emmanuelle
    [J]. STEM CELLS, 2012, 30 (07) : 1327 - 1337
  • [19] An LXR Agonist Promotes Glioblastoma Cell Death through Inhibition of an EGFR/AKT/SREBP-1/LDLR-Dependent Pathway
    Guo, Deliang
    Reinitz, Felicia
    Youssef, Mary
    Hong, Cynthia
    Nathanson, David
    Akhavan, David
    Kuga, Daisuke
    Amzajerdi, Ali Nael
    Soto, Horacio
    Zhu, Shaojun
    Babic, Ivan
    Tanaka, Kazuhiro
    Dang, Julie
    Iwanami, Akio
    Gini, Beatrice
    DeJesus, Jason
    Lisiero, Dominique D.
    Huang, Tiffany T.
    Prins, Robert M.
    Wen, Patrick Y.
    Robins, H. Ian
    Prados, Michael D.
    DeAngelis, Lisa M.
    Mellinghoff, Ingo K.
    Mehta, Minesh P.
    James, C. David
    Chakravarti, Arnab
    Cloughesy, Timothy F.
    Tontonoz, Peter
    Mischel, Paul S.
    [J]. CANCER DISCOVERY, 2011, 1 (05) : 442 - 456
  • [20] Modulation of ER stress and apoptosis by endoplasmic reticulum calcium leak via translocon during unfolded protein response: involvement of GRP78
    Hammadi, Mehdi
    Oulidi, Agathe
    Gackiere, Florian
    Katsogiannou, Maria
    Slomianny, Christian
    Roudbaraki, Morad
    Dewailly, Etienne
    Delcourt, Philippe
    Lepage, Gilbert
    Lotteau, Sabine
    Ducreux, Sylvie
    Prevarskaya, Natalia
    Van Coppenolle, Fabien
    [J]. FASEB JOURNAL, 2013, 27 (04) : 1600 - 1609