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Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure

Cell cycle alterations are among the principle hallmarks of cancer. Consequently, the study of cell cycle regulators has emerged as an important topic in cancer research, particularly in relation to environmental exposure. Particulate matter and coal dust around coal mines have the potential to indu...

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Autores principales: Torres-Ávila, Jose F., Espitia-Pérez, Lyda, Bonatto, Diego, da Silva, Fernanda Rabaioli, de Oliveira, Iuri Marques, Silva, Luís F.O., Corrêa, Dione Silva, Dias, Johnny Ferraz, da Silva, Juliana, Henriques, João Antonio Pêgas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315349/
https://www.ncbi.nlm.nih.gov/pubmed/32609278
http://dx.doi.org/10.1590/1678-4685-GMB-2019-0134
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author Torres-Ávila, Jose F.
Espitia-Pérez, Lyda
Bonatto, Diego
da Silva, Fernanda Rabaioli
de Oliveira, Iuri Marques
Silva, Luís F.O.
Corrêa, Dione Silva
Dias, Johnny Ferraz
da Silva, Juliana
Henriques, João Antonio Pêgas
author_facet Torres-Ávila, Jose F.
Espitia-Pérez, Lyda
Bonatto, Diego
da Silva, Fernanda Rabaioli
de Oliveira, Iuri Marques
Silva, Luís F.O.
Corrêa, Dione Silva
Dias, Johnny Ferraz
da Silva, Juliana
Henriques, João Antonio Pêgas
author_sort Torres-Ávila, Jose F.
collection PubMed
description Cell cycle alterations are among the principle hallmarks of cancer. Consequently, the study of cell cycle regulators has emerged as an important topic in cancer research, particularly in relation to environmental exposure. Particulate matter and coal dust around coal mines have the potential to induce cell cycle alterations. Therefore, in the present study, we performed chemical analyses to identify the main compounds present in two mineral coal samples from Colombian mines and performed systems chemo-biology analysis to elucidate the interactions between these chemical compounds and proteins associated with the cell cycle. Our results highlight the role of oxidative stress generated by the exposure to the residues of coal extraction, such as major inorganic oxides (MIOs), inorganic elements (IEs) and polycyclic aromatic hydrocarbons (PAH) on DNA damage and alterations in the progression of the cell cycle (blockage and/or delay), as well as structural dysfunction in several proteins. In particular, IEs such as Cr, Ni, and S and PAHs such as benzo[a]pyrene may have influential roles in the regulation of the cell cycle through DNA damage and oxidative stress. In this process, cyclins, cyclin-dependent kinases, zinc finger proteins such as TP53, and protein kinases may play a central role.
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spelling pubmed-73153492020-07-06 Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure Torres-Ávila, Jose F. Espitia-Pérez, Lyda Bonatto, Diego da Silva, Fernanda Rabaioli de Oliveira, Iuri Marques Silva, Luís F.O. Corrêa, Dione Silva Dias, Johnny Ferraz da Silva, Juliana Henriques, João Antonio Pêgas Genet Mol Biol Mutagenesis Cell cycle alterations are among the principle hallmarks of cancer. Consequently, the study of cell cycle regulators has emerged as an important topic in cancer research, particularly in relation to environmental exposure. Particulate matter and coal dust around coal mines have the potential to induce cell cycle alterations. Therefore, in the present study, we performed chemical analyses to identify the main compounds present in two mineral coal samples from Colombian mines and performed systems chemo-biology analysis to elucidate the interactions between these chemical compounds and proteins associated with the cell cycle. Our results highlight the role of oxidative stress generated by the exposure to the residues of coal extraction, such as major inorganic oxides (MIOs), inorganic elements (IEs) and polycyclic aromatic hydrocarbons (PAH) on DNA damage and alterations in the progression of the cell cycle (blockage and/or delay), as well as structural dysfunction in several proteins. In particular, IEs such as Cr, Ni, and S and PAHs such as benzo[a]pyrene may have influential roles in the regulation of the cell cycle through DNA damage and oxidative stress. In this process, cyclins, cyclin-dependent kinases, zinc finger proteins such as TP53, and protein kinases may play a central role. Sociedade Brasileira de Genética 2020-06-26 /pmc/articles/PMC7315349/ /pubmed/32609278 http://dx.doi.org/10.1590/1678-4685-GMB-2019-0134 Text en Copyright © 2020, Sociedade Brasileira de Genética. https://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
spellingShingle Mutagenesis
Torres-Ávila, Jose F.
Espitia-Pérez, Lyda
Bonatto, Diego
da Silva, Fernanda Rabaioli
de Oliveira, Iuri Marques
Silva, Luís F.O.
Corrêa, Dione Silva
Dias, Johnny Ferraz
da Silva, Juliana
Henriques, João Antonio Pêgas
Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure
title Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure
title_full Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure
title_fullStr Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure
title_full_unstemmed Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure
title_short Systems chemo-biology analysis of DNA damage response and cell cycle effects induced by coal exposure
title_sort systems chemo-biology analysis of dna damage response and cell cycle effects induced by coal exposure
topic Mutagenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315349/
https://www.ncbi.nlm.nih.gov/pubmed/32609278
http://dx.doi.org/10.1590/1678-4685-GMB-2019-0134
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