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Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers
Bladder cancer is the tenth most common cancer worldwide, where its burden remains a challenge and needs new novel therapies. Several reports indicate expression of CYP4Z1 and CYP1B1 in many tumours. Their expressions are associated with a poor prognosis, and therefore proposed as promising biomarke...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946900/ https://www.ncbi.nlm.nih.gov/pubmed/33692504 http://dx.doi.org/10.1038/s41598-021-85188-4 |
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author | Al-saraireh, Yousef M. Alshammari, Fatemah O. F. O. Youssef, Ahmed M. M. Al-Sarayreh, Sameeh Almuhaisen, Ghadeer H. Alnawaiseh, Nedal Al Shuneigat, Jehad M. Alrawashdeh, Hamzeh M. |
author_facet | Al-saraireh, Yousef M. Alshammari, Fatemah O. F. O. Youssef, Ahmed M. M. Al-Sarayreh, Sameeh Almuhaisen, Ghadeer H. Alnawaiseh, Nedal Al Shuneigat, Jehad M. Alrawashdeh, Hamzeh M. |
author_sort | Al-saraireh, Yousef M. |
collection | PubMed |
description | Bladder cancer is the tenth most common cancer worldwide, where its burden remains a challenge and needs new novel therapies. Several reports indicate expression of CYP4Z1 and CYP1B1 in many tumours. Their expressions are associated with a poor prognosis, and therefore proposed as promising biomarkers or targets for anticancer therapy. By using immunohistochemistry, expression of CYP4Z1 and CYP1B1 was evaluated in a panel of different types of bladder cancer, and the enzymes’ relation to histopathological features were assessed. Results showed an increased expression of CYP4Z1 (54.3%) and CYP1B1 (76.9%) in the majority of bladder cancers compared to weak or lack of expression of both enzymes in normal tissues. CYP4Z1expression was significantly associated with tumour grade and stage where the expression was markedly increased in a high grade and advanced stage of the disease (p < 0.05). Additionally, CYP1B1 expression was also associated with TNM staging (p < 0.05) and its expression was increased in patients with lymph node metastasis. The expression profiles of CYP4Z1 and CYP1B1 suggest that both enzymes have the potential to be biomarkers or targets for novel anticancer therapy for bladder cancer. Nevertheless, further studies are needed to better delineate whether these enzymes are druggable targets. |
format | Online Article Text |
id | pubmed-7946900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79469002021-03-12 Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers Al-saraireh, Yousef M. Alshammari, Fatemah O. F. O. Youssef, Ahmed M. M. Al-Sarayreh, Sameeh Almuhaisen, Ghadeer H. Alnawaiseh, Nedal Al Shuneigat, Jehad M. Alrawashdeh, Hamzeh M. Sci Rep Article Bladder cancer is the tenth most common cancer worldwide, where its burden remains a challenge and needs new novel therapies. Several reports indicate expression of CYP4Z1 and CYP1B1 in many tumours. Their expressions are associated with a poor prognosis, and therefore proposed as promising biomarkers or targets for anticancer therapy. By using immunohistochemistry, expression of CYP4Z1 and CYP1B1 was evaluated in a panel of different types of bladder cancer, and the enzymes’ relation to histopathological features were assessed. Results showed an increased expression of CYP4Z1 (54.3%) and CYP1B1 (76.9%) in the majority of bladder cancers compared to weak or lack of expression of both enzymes in normal tissues. CYP4Z1expression was significantly associated with tumour grade and stage where the expression was markedly increased in a high grade and advanced stage of the disease (p < 0.05). Additionally, CYP1B1 expression was also associated with TNM staging (p < 0.05) and its expression was increased in patients with lymph node metastasis. The expression profiles of CYP4Z1 and CYP1B1 suggest that both enzymes have the potential to be biomarkers or targets for novel anticancer therapy for bladder cancer. Nevertheless, further studies are needed to better delineate whether these enzymes are druggable targets. Nature Publishing Group UK 2021-03-10 /pmc/articles/PMC7946900/ /pubmed/33692504 http://dx.doi.org/10.1038/s41598-021-85188-4 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Al-saraireh, Yousef M. Alshammari, Fatemah O. F. O. Youssef, Ahmed M. M. Al-Sarayreh, Sameeh Almuhaisen, Ghadeer H. Alnawaiseh, Nedal Al Shuneigat, Jehad M. Alrawashdeh, Hamzeh M. Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers |
title | Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers |
title_full | Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers |
title_fullStr | Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers |
title_full_unstemmed | Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers |
title_short | Profiling of CYP4Z1 and CYP1B1 expression in bladder cancers |
title_sort | profiling of cyp4z1 and cyp1b1 expression in bladder cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946900/ https://www.ncbi.nlm.nih.gov/pubmed/33692504 http://dx.doi.org/10.1038/s41598-021-85188-4 |
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