Accumulation of Palmitoylcarnitine and Its Effect on Pro-Inflammatory Pathways and Calcium Influx in Prostate Cancer

被引:35
作者
Al-Bakheit, Ala'a [1 ]
Traka, Maria [2 ]
Saha, Shikha [2 ]
Mithen, Richard [2 ]
Melchini, Antonietta [2 ]
机构
[1] Al Balqa Appl Univ, Dept Nutr & Food Sci, Al Salt, Jordan
[2] Inst Food Res, Food & Hlth Programme, Norwich NR4 7UA, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
acylcarnitines; metabolic disruption; interleukine-6; pathway; intracellular calcium signaling; dihydrotestosterone; FATTY-ACID; L-CARNITINE; ACYLCARNITINES; METABOLISM; PLASMA; CELLS; INTERLEUKIN-6; MODULATION; OXIDATION; PALMITYLCARNITINE;
D O I
10.1002/pros.23222
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
BACKGROUNDAcylcarnitines are intermediates of fatty acid oxidation and accumulate as a consequence of the metabolic dysfunction resulting from the insufficient integration between -oxidation and the tricarboxylic acid (TCA) cycle. The aim of this study was to investigate whether acylcarnitines accumulate in prostate cancer tissue, and whether their biological actions could be similar to those of dihydrotestosterone (DHT), a structurally related compound associated with cancer development. METHODSLevels of palmitoylcarnitine (palcar), a C16:00 acylcarnitine, were measured in prostate tissue using LC-MS/MS. The effect of palcar on inflammatory cytokines and calcium (Ca2+) influx was investigated in in vitro models of prostate cancer. RESULTSWe observed a significantly higher level of palcar in prostate cancerous tissue compared to benign tissue. High levels of palcar have been associated with increased gene expression and secretion of the pro-inflammatory cytokine IL-6 in cancerous PC3 cells, compared to normal PNT1A cells. Furthermore, we found that high levels of palcar induced a rapid Ca2+ influx in PC3 cells, but not in DU145, BPH-1, or PNT1A cells. This pattern of Ca2+ influx was also observed in response to DHT. Through the use of whole genome arrays we demonstrated that PNT1A cells exposed to palcar or DHT have a similar biological response. CONCLUSIONSThis study suggests that palcar might act as a potential mediator for prostate cancer progression through its effect on (i) pro-inflammatory pathways, (ii) Ca2+ influx, and (iii) DHT-like effects. Further studies need to be undertaken to explore whether this class of compounds has different biological functions at physiological and pathological levels. Prostate 76:1326-1337, 2016. (c) 2016 The Authors. The Prostate published by Wiley Periodicals, Inc.
引用
收藏
页码:1326 / 1337
页数:12
相关论文
共 49 条
[1]
ADAMS RJ, 1979, J BIOL CHEM, V254, P2404
[2]
Plasma Acylcarnitine Profiles Suggest Incomplete Long-Chain Fatty Acid β-Oxidation and Altered Tricarboxylic Acid Cycle Activity in Type 2 Diabetic African-American Women [J].
Adams, Sean H. ;
Hoppel, Charles L. ;
Lok, Kerry H. ;
Zhao, Ling ;
Wong, Scott W. ;
Minkler, Paul E. ;
Hwang, Daniel H. ;
Newman, John W. ;
Garvey, W. Timothy .
JOURNAL OF NUTRITION, 2009, 139 (06) :1073-1081
[3]
[Anonymous], UROLOGY
[4]
Bengtsson H., 2008, TECH REP, P1
[5]
Cansino Alcaide Jose Ramon, 2009, Arch Esp Urol, V62, P359
[6]
Androgen-mediated resistance to apoptosis [J].
Coffey, RNT ;
Watson, RWG ;
O'Neill, AJ ;
Mc Eleny, K ;
Fitzpatrick, JM .
PROSTATE, 2002, 53 (04) :300-309
[7]
Altered metabolism and mitochondrial genome in prostate cancer [J].
Dakubo, GD ;
Parr, RL ;
Costello, LC ;
Franklin, RB ;
Thayer, RE .
JOURNAL OF CLINICAL PATHOLOGY, 2006, 59 (01) :10-16
[8]
MODULATION OF CANINE MYOCARDIAL SARCOLEMMAL MEMBRANE FLUIDITY BY AMPHIPHILIC COMPOUNDS [J].
FINK, KL ;
GROSS, RW .
CIRCULATION RESEARCH, 1984, 55 (05) :585-594
[9]
Urinary acylcarnitines are altered in human kidney cancer [J].
Ganti, Sheila ;
Taylor, Sandra L. ;
Kim, Kyoungmi ;
Hoppel, Charles L. ;
Guo, Lining ;
Yang, Joy ;
Evans, Christopher ;
Weiss, Robert H. .
INTERNATIONAL JOURNAL OF CANCER, 2012, 130 (12) :2791-2800
[10]
Bioconductor: open software development for computational biology and bioinformatics [J].
Gentleman, RC ;
Carey, VJ ;
Bates, DM ;
Bolstad, B ;
Dettling, M ;
Dudoit, S ;
Ellis, B ;
Gautier, L ;
Ge, YC ;
Gentry, J ;
Hornik, K ;
Hothorn, T ;
Huber, W ;
Iacus, S ;
Irizarry, R ;
Leisch, F ;
Li, C ;
Maechler, M ;
Rossini, AJ ;
Sawitzki, G ;
Smith, C ;
Smyth, G ;
Tierney, L ;
Yang, JYH ;
Zhang, JH .
GENOME BIOLOGY, 2004, 5 (10)