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Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms
According to International Agency for Research on Cancer, ethanol and acetaldehyde belong to group 1 of human carcinogens. The accurate mechanism by which alcohol consumption enhances carcinogenesis is still unexplained. Alcohol is oxidized primarily by alcohol dehydrogenase (ADH) to acetaldehyde, a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403859/ https://www.ncbi.nlm.nih.gov/pubmed/26886278 http://dx.doi.org/10.1007/s10238-016-0408-3 |
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author | Orywal, Karolina Szmitkowski, Maciej |
author_facet | Orywal, Karolina Szmitkowski, Maciej |
author_sort | Orywal, Karolina |
collection | PubMed |
description | According to International Agency for Research on Cancer, ethanol and acetaldehyde belong to group 1 of human carcinogens. The accurate mechanism by which alcohol consumption enhances carcinogenesis is still unexplained. Alcohol is oxidized primarily by alcohol dehydrogenase (ADH) to acetaldehyde, a substance capable of initiating carcinogenesis by forming adducts with proteins and DNA and causing mutations. Next, acetaldehyde is metabolized by aldehyde dehydrogenase (ALDH) to acetate. In tissues of many cancers, we can observe significantly higher activity of total alcohol dehydrogenase with any change in aldehyde dehydrogenase activity in comparison with healthy cells. Moreover, in malignant diseases of digestive system, significantly increased activity of ADH isoenzymes class I, III and IV was found. The gynecological, brain and renal cancers exhibit increased activity of class I ADH. ADH and ALDH can play also a crucial regulatory role in initiation and progression of malignant diseases by participation in retinoic acid synthesis and elimination of toxic acetaldehyde. Besides, changes of enzymes activities in tumor cells are reflected in serum of cancer patients, which create the possibilities of application ADH isoenzymes as cancer markers. |
format | Online Article Text |
id | pubmed-5403859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-54038592017-05-09 Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms Orywal, Karolina Szmitkowski, Maciej Clin Exp Med Review Article According to International Agency for Research on Cancer, ethanol and acetaldehyde belong to group 1 of human carcinogens. The accurate mechanism by which alcohol consumption enhances carcinogenesis is still unexplained. Alcohol is oxidized primarily by alcohol dehydrogenase (ADH) to acetaldehyde, a substance capable of initiating carcinogenesis by forming adducts with proteins and DNA and causing mutations. Next, acetaldehyde is metabolized by aldehyde dehydrogenase (ALDH) to acetate. In tissues of many cancers, we can observe significantly higher activity of total alcohol dehydrogenase with any change in aldehyde dehydrogenase activity in comparison with healthy cells. Moreover, in malignant diseases of digestive system, significantly increased activity of ADH isoenzymes class I, III and IV was found. The gynecological, brain and renal cancers exhibit increased activity of class I ADH. ADH and ALDH can play also a crucial regulatory role in initiation and progression of malignant diseases by participation in retinoic acid synthesis and elimination of toxic acetaldehyde. Besides, changes of enzymes activities in tumor cells are reflected in serum of cancer patients, which create the possibilities of application ADH isoenzymes as cancer markers. Springer International Publishing 2016-02-17 2017 /pmc/articles/PMC5403859/ /pubmed/26886278 http://dx.doi.org/10.1007/s10238-016-0408-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review Article Orywal, Karolina Szmitkowski, Maciej Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
title | Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
title_full | Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
title_fullStr | Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
title_full_unstemmed | Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
title_short | Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
title_sort | alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403859/ https://www.ncbi.nlm.nih.gov/pubmed/26886278 http://dx.doi.org/10.1007/s10238-016-0408-3 |
work_keys_str_mv | AT orywalkarolina alcoholdehydrogenaseandaldehydedehydrogenaseinmalignantneoplasms AT szmitkowskimaciej alcoholdehydrogenaseandaldehydedehydrogenaseinmalignantneoplasms |