Literature DB >> 15020846

Ethanol treatment of hepatocellular carcinoma: high potentials of low concentrations.

Francisco Castaneda1, Rolf K-H Kinne.   

Abstract

Primary hepatocellular carcinoma (HCC) is one of the most common malignant tumors worldwide, which is associated with a very poor prognosis. A curative treatment is difficult to achieve and is only possible in a low number of patients. Therefore, many different therapeutic strategies have been developed as alternative treatment. Among these, percutaneous injection of high concentrations of ethanol (>50 mM) has been proven to be effective for the treatment of small HCC (less than 3 cm in diameter). However, the principal problem with using ethanol is its toxic effects on non-tumor cells adjacent to the tumor area. The objective of this review is to juxtapose the therapeutic potential of high and low concentrations of ethanol in the treatment of HCC, based on experimental studies obtained with the human hepatocellular tumor cell line (HepG2). They have shown that high concentrations of ethanol lead to necrosis, while low concentrations induce apoptosis due to activation of Fas-receptors. Triggering of apoptosis through Fas-receptors represents a mechanism of action different from that observed with high concentrations of ethanol, thus, reducing the complications that follow the inflammatory process due to necrosis. Therefore, the use of low concentrations of ethanol could be an effective treatment for HCC.

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Year:  2004        PMID: 15020846     DOI: 10.4161/cbt.3.5.806

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


  7 in total

1.  Drug-eluting microarrays for cell-based screening of chemical-induced apoptosis.

Authors:  Cheong Hoon Kwon; Ian Wheeldon; Nezamoddin N Kachouie; Seung Hwan Lee; Hojae Bae; Shilpa Sant; Junji Fukuda; Jeong Won Kang; Ali Khademhosseini
Journal:  Anal Chem       Date:  2011-05-03       Impact factor: 6.986

2.  Coenzyme Q10 reduces ethanol-induced apoptosis in corneal fibroblasts.

Authors:  Chun-Chen Chen; Shiow-Wen Liou; Chi-Chih Chen; Wen-Chung Chen; Fung-Rong Hu; I-Jong Wang; Shing-Jong Lin
Journal:  PLoS One       Date:  2011-04-27       Impact factor: 3.240

3.  Functional genomics analysis of low concentration of ethanol in human hepatocellular carcinoma (HepG2) cells. Role of genes involved in transcriptional and translational processes.

Authors:  Francisco Castaneda; Sigrid Rosin-Steiner; Klaus Jung
Journal:  Int J Med Sci       Date:  2006-12-21       Impact factor: 3.738

4.  Low concentration of ethanol induce apoptosis in HepG2 cells: role of various signal transduction pathways.

Authors:  Francisco Castaneda; Sigrid Rosin-Steiner
Journal:  Int J Med Sci       Date:  2006-10-31       Impact factor: 3.738

5.  Protective Effect of Tyrosol and S-Adenosylmethionine against Ethanol-Induced Oxidative Stress of Hepg2 Cells Involves Sirtuin 1, P53 and Erk1/2 Signaling.

Authors:  Paola Stiuso; Maria Libera Bagarolo; Concetta Paola Ilisso; Daniela Vanacore; Elisa Martino; Michele Caraglia; Marina Porcelli; Giovanna Cacciapuoti
Journal:  Int J Mol Sci       Date:  2016-04-26       Impact factor: 5.923

6.  Dihydromyricetin Protects the Liver via Changes in Lipid Metabolism and Enhanced Ethanol Metabolism.

Authors:  Joshua Silva; Xin Yu; Renita Moradian; Carson Folk; Maximilian H Spatz; Phoebe Kim; Adil A Bhatti; Daryl L Davies; Jing Liang
Journal:  Alcohol Clin Exp Res       Date:  2020-04-08       Impact factor: 3.455

7.  Phenotypic alterations in liver cancer cells induced by mechanochemical disruption.

Authors:  Hakm Y Murad; Emma P Bortz; Heng Yu; Daishen Luo; Gray M Halliburton; Andrew B Sholl; Damir B Khismatullin
Journal:  Sci Rep       Date:  2019-12-20       Impact factor: 4.379

  7 in total

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