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Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity
Ovarian cancer is the second most common gynaecologic malignancy and the main cause of death from gynaecologic cancer, due to late diagnosis and chemoresistance. Studies have reported the role of cysteine in cancer, by contributing for hydrogen sulphide (H(2)S) generation and as a precursor of gluta...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015047/ https://www.ncbi.nlm.nih.gov/pubmed/29934500 http://dx.doi.org/10.1038/s41598-018-27753-y |
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author | Nunes, Sofia C. Ramos, Cristiano Lopes-Coelho, Filipa Sequeira, Catarina O. Silva, Fernanda Gouveia-Fernandes, Sofia Rodrigues, Armanda Guimarães, António Silveira, Margarida Abreu, Sofia Santo, Vítor E. Brito, Catarina Félix, Ana Pereira, Sofia A. Serpa, Jacinta |
author_facet | Nunes, Sofia C. Ramos, Cristiano Lopes-Coelho, Filipa Sequeira, Catarina O. Silva, Fernanda Gouveia-Fernandes, Sofia Rodrigues, Armanda Guimarães, António Silveira, Margarida Abreu, Sofia Santo, Vítor E. Brito, Catarina Félix, Ana Pereira, Sofia A. Serpa, Jacinta |
author_sort | Nunes, Sofia C. |
collection | PubMed |
description | Ovarian cancer is the second most common gynaecologic malignancy and the main cause of death from gynaecologic cancer, due to late diagnosis and chemoresistance. Studies have reported the role of cysteine in cancer, by contributing for hydrogen sulphide (H(2)S) generation and as a precursor of glutathione (GSH). However, the role of cysteine in the adaptation to hypoxia and therapy response remains unclear. We used several ovarian cancer cell lines, ES2, OVCAR3, OVCAR8, A2780 and A2780cisR, to clarify cysteine relevance in ovarian cancer cells survival upon hypoxia and carboplatin. Results show that ES2 and OVCAR8 cells presented a stronger dependence on cysteine availability upon hypoxia and carboplatin exposure than OVCAR3 cells. Interestingly, the A2780 cisR, but not A2780 parental cells, benefits from cysteine upon carboplatin exposure, showing that cysteine is crucial for chemoresistance. Moreover, GSH degradation and subsequent cysteine recycling pathway is associated with ovarian cancer as seen in peripheral blood serum from patients. Higher levels of total free cysteine (Cys) and homocysteine (HCys) were found in ovarian cancer patients in comparison with benign tumours and lower levels of GSH were found in ovarian neoplasms patients in comparison with healthy individuals. Importantly, the total and S-Homocysteinylated levels distinguished blood donors from patients with neoplasms as well as patients with benign from patients with malignant tumours. The levels of S-cysteinylated proteins distinguish blood donors from patients with neoplasms and the free levels of Cys in serum distinguish blood from patients with benign tumours from patients with malignant tumours. Herein we disclosed that cysteine contributes for a worse disease prognosis, allowing faster adaptation to hypoxia and protecting cells from carboplatin. The measurement of serum cysteine levels can be an effective tool for early diagnosis, for outcome prediction and follow up of disease progression. |
format | Online Article Text |
id | pubmed-6015047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60150472018-07-06 Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity Nunes, Sofia C. Ramos, Cristiano Lopes-Coelho, Filipa Sequeira, Catarina O. Silva, Fernanda Gouveia-Fernandes, Sofia Rodrigues, Armanda Guimarães, António Silveira, Margarida Abreu, Sofia Santo, Vítor E. Brito, Catarina Félix, Ana Pereira, Sofia A. Serpa, Jacinta Sci Rep Article Ovarian cancer is the second most common gynaecologic malignancy and the main cause of death from gynaecologic cancer, due to late diagnosis and chemoresistance. Studies have reported the role of cysteine in cancer, by contributing for hydrogen sulphide (H(2)S) generation and as a precursor of glutathione (GSH). However, the role of cysteine in the adaptation to hypoxia and therapy response remains unclear. We used several ovarian cancer cell lines, ES2, OVCAR3, OVCAR8, A2780 and A2780cisR, to clarify cysteine relevance in ovarian cancer cells survival upon hypoxia and carboplatin. Results show that ES2 and OVCAR8 cells presented a stronger dependence on cysteine availability upon hypoxia and carboplatin exposure than OVCAR3 cells. Interestingly, the A2780 cisR, but not A2780 parental cells, benefits from cysteine upon carboplatin exposure, showing that cysteine is crucial for chemoresistance. Moreover, GSH degradation and subsequent cysteine recycling pathway is associated with ovarian cancer as seen in peripheral blood serum from patients. Higher levels of total free cysteine (Cys) and homocysteine (HCys) were found in ovarian cancer patients in comparison with benign tumours and lower levels of GSH were found in ovarian neoplasms patients in comparison with healthy individuals. Importantly, the total and S-Homocysteinylated levels distinguished blood donors from patients with neoplasms as well as patients with benign from patients with malignant tumours. The levels of S-cysteinylated proteins distinguish blood donors from patients with neoplasms and the free levels of Cys in serum distinguish blood from patients with benign tumours from patients with malignant tumours. Herein we disclosed that cysteine contributes for a worse disease prognosis, allowing faster adaptation to hypoxia and protecting cells from carboplatin. The measurement of serum cysteine levels can be an effective tool for early diagnosis, for outcome prediction and follow up of disease progression. Nature Publishing Group UK 2018-06-22 /pmc/articles/PMC6015047/ /pubmed/29934500 http://dx.doi.org/10.1038/s41598-018-27753-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nunes, Sofia C. Ramos, Cristiano Lopes-Coelho, Filipa Sequeira, Catarina O. Silva, Fernanda Gouveia-Fernandes, Sofia Rodrigues, Armanda Guimarães, António Silveira, Margarida Abreu, Sofia Santo, Vítor E. Brito, Catarina Félix, Ana Pereira, Sofia A. Serpa, Jacinta Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
title | Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
title_full | Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
title_fullStr | Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
title_full_unstemmed | Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
title_short | Cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
title_sort | cysteine allows ovarian cancer cells to adapt to hypoxia and to escape from carboplatin cytotoxicity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015047/ https://www.ncbi.nlm.nih.gov/pubmed/29934500 http://dx.doi.org/10.1038/s41598-018-27753-y |
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