Bile acids: From digestion to cancers

被引:82
作者
Baptissart, Marine [1 ,2 ,3 ,4 ]
Vega, Aurelie [1 ,2 ,3 ,4 ]
Maqdasy, Salwan [1 ,2 ,3 ,4 ,5 ,6 ]
Caira, Francoise [1 ,2 ,3 ,4 ]
Baron, Silvere [1 ,2 ,3 ,4 ]
Lobaccaro, Jean-Marc A. [1 ,2 ,3 ,4 ]
Volle, David H. [1 ,2 ,3 ,4 ]
机构
[1] INSERM, U1103, F-63177 Aubiere, France
[2] Univ Blaise Pascal, Clermont Univ, F-63000 Clermont Ferrand, France
[3] Univ Clermont Ferrand 2, Photochim Mol & Macromol Lab, CNRS, UMR 6293, F-63177 Aubiere, France
[4] Ctr Rech Nutr Humaine Auvergne, F-63000 Clermont Ferrand, France
[5] Ctr Hosp Univ, Serv Endocrinol, F-63000 Clermont Ferrand, France
[6] Univ Auvergne, F-63000 Clermont Ferrand, France
关键词
Bile acids; FXR alpha; TGR5; Cancer; FARNESOID-X-RECEPTOR; NF-KAPPA-B; SMALL HETERODIMER PARTNER; GASTROESOPHAGEAL-REFLUX DISEASE; DYSPLASIA-CARCINOMA SEQUENCE; SOLUTE TRANSPORTER-ALPHA; NONALCOHOLIC FATTY LIVER; ACTIVATED PROTEIN-KINASE; NUCLEAR RECEPTOR; DEOXYCHOLIC-ACID;
D O I
10.1016/j.biochi.2012.06.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bile acids (BAs) are cholesterol metabolites that have been extensively studied these last decades. BAs have been classified in two groups. Primary BAs are synthesized in liver, when secondary BAs are produced by intestinal bacteria. Recently, next to their ancestral roles in digestion and fat solubilization, BAs have been described as signaling molecules involved in many physiological functions, such as glucose and energy metabolisms. These signaling pathways involve the activation of the nuclear receptor FXR alpha: or of the G-protein-coupled receptor TGR5. These two receptors have selective affinity to different types of BAs and show different expression patterns, leading to different described roles of BAs. It has been suggested for long that BAs could be molecules linked to tumor processes. Indeed, as many other molecules, regarding analyzed tissues, BAs could have either protective or pro-carcinogen activities. However, the molecular mechanisms responsible for these effects have not been characterized yet. It involves either chemical properties or their capacities to activate their specific receptors FXR alpha or TGR5. This review highlights and discusses the potential links between BAs and cancer diseases and the perspectives of using BAs as potential therapeutic targets in several pathologies. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:504 / 517
页数:14
相关论文
共 161 条
[1]   Role of genes, the environment and their interactions in the etiology of inflammatory bowel diseases [J].
Ahmed, Farid E. .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2006, 6 (03) :345-363
[2]   Bile acid transporters: Structure, function, regulation and pathophysiological implications [J].
Alrefai, Waddah A. ;
Gill, Ravinder K. .
PHARMACEUTICAL RESEARCH, 2007, 24 (10) :1803-1823
[3]   Human bile salt export pump promoter is transactivated by the farnesoid X receptor/bile acid receptor [J].
Ananthanarayanan, M ;
Balasubramanian, N ;
Makishima, M ;
Mangelsdorf, DJ ;
Suchy, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (31) :28857-28865
[4]  
Arthur MJP, 2000, AM J PHYSIOL-GASTR L, V279, pG245
[5]   Bile acids: short and long term effects in the intestine [J].
Bajor, Antal ;
Gillberg, Per-Goran ;
Abrahamsson, Hasse .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2010, 45 (06) :645-664
[6]   The Interaction of a High-Fat Diet and Regular Moderate Intensity Exercise on Intestinal Polyp Development in ApcMin/+ Mice [J].
Baltgalvis, Kristen A. ;
Berger, Franklin G. ;
Pena, Maria Marjorette O. ;
Davis, J. Mark ;
Carson, James A. .
CANCER PREVENTION RESEARCH, 2009, 2 (07) :641-649
[7]   FXR induces the UGT2B4 enzyme in hepatocytes: A potential mechanism of negative feedback control of FXR activity [J].
Barbier, O ;
Torra, IP ;
Sirvent, A ;
Claudel, T ;
Blanquart, C ;
Duran-Sandoval, D ;
Kuipers, F ;
Kosykh, V ;
Fruchart, JC ;
Staels, B .
GASTROENTEROLOGY, 2003, 124 (07) :1926-1940
[8]   Activation of the promoters of genes associated with DNA damage, oxidative stress, ER stress and protein malfolding by the bile salt, deoxycholate [J].
Bernstein, H ;
Payne, CM ;
Bernstein, C ;
Schneider, J ;
Beard, SE ;
Crowley, CL .
TOXICOLOGY LETTERS, 1999, 108 (01) :37-46
[9]   Unique dietary-related mouse model of colitis [J].
Bernstein, H ;
Holubec, H ;
Bernstein, C ;
Ignatenko, N ;
Gerner, E ;
Dvorak, K ;
Besselsen, D ;
Ramsey, L ;
Dall'Agnol, M ;
Blohm-Mangone, KA ;
Padilla-Torres, J ;
Cui, HY ;
Garewal, H ;
Payne, CM .
INFLAMMATORY BOWEL DISEASES, 2006, 12 (04) :278-293
[10]   Risk factors associated with non-alcoholic fatty liver disease in subjects from primary care units. A case-control study [J].
Caballeria, Llorenc ;
Antonia Auladell, Ma ;
Toran, Pere ;
Pera, Guillem ;
Miranda, Dolores ;
Aluma, Alba ;
Casas, Jose Dario ;
Munoz, Laura ;
Sanchez, Carmen ;
Tibau, Albert ;
Birules, Marti ;
Canut, Santiago ;
Bernad, Jesus ;
Auba, Josep ;
Maite Aizpurua, Miren ;
Alcaraz, Enriqueta .
BMC GASTROENTEROLOGY, 2008, 8 (1)