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Cystathionine β-Synthase in Physiology and Cancer

Cystathionine β-synthase (CBS) regulates homocysteine metabolism and contributes to hydrogen sulfide (H(2)S) biosynthesis through which it plays multifunctional roles in the regulation of cellular energetics, redox status, DNA methylation, and protein modification. Inactivating mutations in CBS cont...

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Detalles Bibliográficos
Autores principales: Zhu, Haoran, Blake, Shaun, Chan, Keefe T., Pearson, Richard B., Kang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046153/
https://www.ncbi.nlm.nih.gov/pubmed/30050925
http://dx.doi.org/10.1155/2018/3205125
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author Zhu, Haoran
Blake, Shaun
Chan, Keefe T.
Pearson, Richard B.
Kang, Jian
author_facet Zhu, Haoran
Blake, Shaun
Chan, Keefe T.
Pearson, Richard B.
Kang, Jian
author_sort Zhu, Haoran
collection PubMed
description Cystathionine β-synthase (CBS) regulates homocysteine metabolism and contributes to hydrogen sulfide (H(2)S) biosynthesis through which it plays multifunctional roles in the regulation of cellular energetics, redox status, DNA methylation, and protein modification. Inactivating mutations in CBS contribute to the pathogenesis of the autosomal recessive disease CBS-deficient homocystinuria. Recent studies demonstrating that CBS promotes colon and ovarian cancer growth in preclinical models highlight a newly identified oncogenic role for CBS. On the contrary, tumor-suppressive effects of CBS have been reported in other cancer types, suggesting context-dependent roles of CBS in tumor growth and progression. Here, we review the physiological functions of CBS, summarize the complexities regarding CBS research in oncology, and discuss the potential of CBS and its key metabolites, including homocysteine and H(2)S, as potential biomarkers for cancer diagnosis or therapeutic targets for cancer treatment.
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spelling pubmed-60461532018-07-26 Cystathionine β-Synthase in Physiology and Cancer Zhu, Haoran Blake, Shaun Chan, Keefe T. Pearson, Richard B. Kang, Jian Biomed Res Int Review Article Cystathionine β-synthase (CBS) regulates homocysteine metabolism and contributes to hydrogen sulfide (H(2)S) biosynthesis through which it plays multifunctional roles in the regulation of cellular energetics, redox status, DNA methylation, and protein modification. Inactivating mutations in CBS contribute to the pathogenesis of the autosomal recessive disease CBS-deficient homocystinuria. Recent studies demonstrating that CBS promotes colon and ovarian cancer growth in preclinical models highlight a newly identified oncogenic role for CBS. On the contrary, tumor-suppressive effects of CBS have been reported in other cancer types, suggesting context-dependent roles of CBS in tumor growth and progression. Here, we review the physiological functions of CBS, summarize the complexities regarding CBS research in oncology, and discuss the potential of CBS and its key metabolites, including homocysteine and H(2)S, as potential biomarkers for cancer diagnosis or therapeutic targets for cancer treatment. Hindawi 2018-06-28 /pmc/articles/PMC6046153/ /pubmed/30050925 http://dx.doi.org/10.1155/2018/3205125 Text en Copyright © 2018 Haoran Zhu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Zhu, Haoran
Blake, Shaun
Chan, Keefe T.
Pearson, Richard B.
Kang, Jian
Cystathionine β-Synthase in Physiology and Cancer
title Cystathionine β-Synthase in Physiology and Cancer
title_full Cystathionine β-Synthase in Physiology and Cancer
title_fullStr Cystathionine β-Synthase in Physiology and Cancer
title_full_unstemmed Cystathionine β-Synthase in Physiology and Cancer
title_short Cystathionine β-Synthase in Physiology and Cancer
title_sort cystathionine β-synthase in physiology and cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046153/
https://www.ncbi.nlm.nih.gov/pubmed/30050925
http://dx.doi.org/10.1155/2018/3205125
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