Literature DB >> 22766017

Bile acids: from digestion to cancers.

Marine Baptissart1, Aurelie Vega, Salwan Maqdasy, Françoise Caira, Silvère Baron, Jean-Marc A Lobaccaro, David H Volle.   

Abstract

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 FXRα 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 FXRα 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.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

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Year:  2012        PMID: 22766017     DOI: 10.1016/j.biochi.2012.06.022

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  37 in total

1.  Tsumura-Suzuki obese diabetic mice-derived hepatic tumors closely resemble human hepatocellular carcinomas in metabolism-related genes expression and bile acid accumulation.

Authors:  Tetsuyuki Takahashi; Ulrich Deuschle; Shu Taira; Takeshi Nishida; Makoto Fujimoto; Takao Hijikata; Koichi Tsuneyama
Journal:  Hepatol Int       Date:  2018-04-12       Impact factor: 6.047

2.  Synthesis, Structure-Activity Relationship, and Mechanistic Investigation of Lithocholic Acid Amphiphiles for Colon Cancer Therapy.

Authors:  Manish Singh; Sandhya Bansal; Somanath Kundu; Priyanshu Bhargava; Ashima Singh; Rajender K Motiani; Radhey Shyam; Vedagopuram Sreekanth; Sagar Sengupta; Avinash Bajaj
Journal:  Medchemcomm       Date:  2014-10-15       Impact factor: 3.597

3.  Dynamic changes of the luminal and mucosa-associated gut microbiota during and after antibiotic therapy with paromomycin.

Authors:  Femke-Anouska Heinsen; Henrik Knecht; Sven C Neulinger; Ruth A Schmitz; Carolin Knecht; Tanja Kühbacher; Philip C Rosenstiel; Stefan Schreiber; Anette K Friedrichs; Stephan J Ott
Journal:  Gut Microbes       Date:  2015-07-04

Review 4.  Hepatocellular carcinoma mouse models: Hepatitis B virus-associated hepatocarcinogenesis and haploinsufficient tumor suppressor genes.

Authors:  Yuan-Chi Teng; Zhao-Qing Shen; Cheng-Heng Kao; Ting-Fen Tsai
Journal:  World J Gastroenterol       Date:  2016-01-07       Impact factor: 5.742

Review 5.  Bile acid dysregulation, gut dysbiosis, and gastrointestinal cancer.

Authors:  Jessica Tsuei; Thinh Chau; David Mills; Yu-Jui Yvonne Wan
Journal:  Exp Biol Med (Maywood)       Date:  2014-06-20

6.  Bile acids promote diethylnitrosamine-induced hepatocellular carcinoma via increased inflammatory signaling.

Authors:  Lina Sun; Kevin Beggs; Prachi Borude; Genea Edwards; Bharat Bhushan; Chad Walesky; Nairita Roy; Michael W Manley; Sumedha Gunewardena; Maura O'Neil; Hua Li; Udayan Apte
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2016-05-05       Impact factor: 4.052

Review 7.  Farnesoid X receptor alpha (FXRα) is a critical actor of the development and pathologies of the male reproductive system.

Authors:  Manon Garcia; Laura Thirouard; Mélusine Monrose; Hélène Holota; Angélique De Haze; Françoise Caira; Claude Beaudoin; David H Volle
Journal:  Cell Mol Life Sci       Date:  2019-08-12       Impact factor: 9.261

8.  Bile Acid Receptors and Liver Cancer.

Authors:  Xichun Wang; Xianghui Fu; Carl Van Ness; Zhipeng Meng; Xiaoxiao Ma; Wendong Huang
Journal:  Curr Pathobiol Rep       Date:  2012-12-21

9.  Activation of bile acid signaling improves metabolic phenotypes in high-fat diet-induced obese mice.

Authors:  Joseph F Pierre; Kristina B Martinez; Honggang Ye; Anuradha Nadimpalli; Timothy C Morton; Jinghui Yang; Qiang Wang; Noelle Patno; Eugene B Chang; Deng Ping Yin
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2016-06-23       Impact factor: 4.052

10.  Bile acids-mediated overexpression of MUC4 via FAK-dependent c-Jun activation in pancreatic cancer.

Authors:  Suhasini Joshi; Eric Cruz; Satyanarayana Rachagani; Sushovan Guha; Randall E Brand; Moorthy P Ponnusamy; Sushil Kumar; Surinder K Batra
Journal:  Mol Oncol       Date:  2016-04-29       Impact factor: 6.603

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