Literature DB >> 17431106

Molecular mechanisms of the chemopreventive effect on hepatocellular carcinoma development in Mdr2 knockout mice.

Mark Katzenellenbogen1, Lina Mizrahi, Orit Pappo, Naama Klopstock, Devorah Olam, Hila Barash, Eytan Domany, Eithan Galun, Daniel Goldenberg.   

Abstract

Dietary antioxidants and selenium compounds were shown to have a therapeutic effect against hepatocellular carcinoma in several mouse models. We tested the effects of tannic acid and selenomethionine on hepatocellular carcinoma development in Mdr2 knockout (Mdr2-KO) mice. Mdr2-KO and age-matched Mdr2 heterozygous control mice were fed with tannic acid or selenomethionine during the first 3 months of life. Then, several mice from each group were sacrificed, and liver tissue samples were removed for analysis. The remaining mice were fed a regular diet until the age of 16 months, at which time the number and size of liver tumors were determined. Liver tissue samples of 3-month-old mice were subjected to gene expression profiling analysis using cDNA macroarrays containing probes for 240 genes that regulate responses to oxidative stress and inflammation or lipid metabolism. Both tannic acid and selenomethionine had partial chemopreventive effect on development of hepatocellular carcinoma in Mdr2-KO mice: they reduced the incidence of large tumor nodules (diameter >1 cm) at age 16 months. Both agents inhibited gene expression and reversed up-regulation of many genes that control inflammation or response to oxidative stress in Mdr2-KO livers at age 3 months. This inhibitory effect on gene expression correlated with the ability of agents to reduce incidence of large tumors: selenomethionine was more active than tannic acid in both aspects. Understanding the molecular mechanism of chemoprevention effect could improve our therapeutic modalities while using these agents.

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Year:  2007        PMID: 17431106     DOI: 10.1158/1535-7163.MCT-06-0420

Source DB:  PubMed          Journal:  Mol Cancer Ther        ISSN: 1535-7163            Impact factor:   6.261


  8 in total

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3.  Tumor-suppressive effect of S-adenosylmethionine supplementation in a murine model of inflammation-mediated hepatocarcinogenesis is dependent on treatment longevity.

Authors:  Evgeniy Stoyanov; Lina Mizrahi; Devorah Olam; Temima Schnitzer-Perlman; Eithan Galun; Daniel S Goldenberg
Journal:  Oncotarget       Date:  2017-05-30

4.  Sustained activation of detoxification pathways promotes liver carcinogenesis in response to chronic bile acid-mediated damage.

Authors:  Agnese Collino; Alberto Termanini; Paola Nicoli; Giuseppe Diaferia; Sara Polletti; Camilla Recordati; Vittoria Castiglioni; Donatella Caruso; Nico Mitro; Gioacchino Natoli; Serena Ghisletti
Journal:  PLoS Genet       Date:  2018-05-07       Impact factor: 5.917

5.  Increased miR-221 expression in hepatocellular carcinoma tissues and its role in enhancing cell growth and inhibiting apoptosis in vitro.

Authors:  Minhua Rong; Gang Chen; Yiwu Dang
Journal:  BMC Cancer       Date:  2013-01-16       Impact factor: 4.430

6.  Natural borneol, a monoterpenoid compound, potentiates selenocystine-induced apoptosis in human hepatocellular carcinoma cells by enhancement of cellular uptake and activation of ROS-mediated DNA damage.

Authors:  Jianyu Su; Haoqiang Lai; Jianping Chen; Lin Li; Yum-Shing Wong; Tianfeng Chen; Xiaoling Li
Journal:  PLoS One       Date:  2013-05-20       Impact factor: 3.240

7.  HCV tumor promoting effect is dependent on host genetic background.

Authors:  Naama Klopstock; Mark Katzenellenbogen; Orit Pappo; Miriam Sklair-Levy; Devorah Olam; Lina Mizrahi; Tamara Potikha; Eithan Galun; Daniel Goldenberg
Journal:  PLoS One       Date:  2009-04-02       Impact factor: 3.240

8.  MicroRNA expression patterns and function in endodermal differentiation of human embryonic stem cells.

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Journal:  PLoS One       Date:  2008-11-18       Impact factor: 3.240

  8 in total

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