Targeting lipid metabolism in metastatic prostate cancer

被引:15
|
作者
Scheinberg, Tahlia [1 ,2 ,3 ]
Mak, Blossom [1 ,2 ,3 ]
Butler, Lisa [4 ,5 ,6 ]
Selth, Luke [5 ,6 ,7 ,8 ]
Horvath, Lisa G. [2 ,3 ,9 ]
机构
[1] Chris OBrien Lifehouse, Med Oncol, Camperdown, NSW, Australia
[2] Garvan Inst Med Res, Adv Prostate Canc Grp, Darlinghurst, NSW, Australia
[3] Univ Sydney, Camperdown, NSW, Australia
[4] South Australian Hlth & Med Res Inst, Prostate Canc Res Grp, Adelaide, SA, Australia
[5] Univ Adelaide, South Australian Immunogen Canc Inst, Adelaide, SA, Australia
[6] Univ Adelaide, Freemasons Ctr Male Hlth & Wellbeing, Adelaide, SA, Australia
[7] Univ Adelaide, Adelaide Med Sch, Dame Roma Mitchell Canc Res Labs, Adelaide, SA, Australia
[8] Flinders Univ S Australia, Flinders Hlth & Med Res Inst, Coll Med & Publ Hlth, Bedford Pk, SA, Australia
[9] Chris OBrien Lifehouse, Med Oncol, Missenden Rd, Camperdown, NSW 2050, Australia
基金
英国医学研究理事会;
关键词
prostate cancer; lipids; targeted therapy; high-fat diet; BODY-MASS INDEX; HIGH-FAT DIET; ANDROGEN-DEPRIVATION THERAPY; CHOLESTEROL-LOWERING DRUGS; TYPE-2; DIABETES-MELLITUS; CORONARY-ARTERY-DISEASE; STATIN USE; RADICAL PROSTATECTOMY; METFORMIN USE; BIOCHEMICAL RECURRENCE;
D O I
10.1177/17588359231152839
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite key advances in the treatment of prostate cancer (PCa), a proportion of men have de novo resistance, and all will develop resistance to current therapeutics over time. Aberrant lipid metabolism has long been associated with prostate carcinogenesis and progression, but more recently there has been an explosion of preclinical and clinical data which is informing new clinical trials. This review explores the epidemiological links between obesity and metabolic syndrome and PCa, the evidence for altered circulating lipids in PCa and their potential role as biomarkers, as well as novel therapeutic strategies for targeting lipids in men with PCa, including therapies widely used in cardiovascular disease such as statins, metformin and lifestyle modification, as well as novel targeted agents such as sphingosine kinase inhibitors, DES1 inhibitors and agents targeting FASN and beta oxidation.
引用
收藏
页数:30
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