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BARD1 mystery: tumor suppressors are cancer susceptibility genes

The full-length BRCA1-associated RING domain 1 (BARD1) gene encodes a 777-aa protein. BARD1 displays a dual role in cancer development and progression as it acts as a tumor suppressor and an oncogene. Structurally, BARD1 has homologous domains to BRCA1 that aid their heterodimer interaction to inhib...

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Autores principales: Hawsawi, Yousef M., Shams, Anwar, Theyab, Abdulrahman, Abdali, Wed A., Hussien, Nahed A., Alatwi, Hanan E., Alzahrani, Othman R., Oyouni, Atif Abdulwahab A., Babalghith, Ahmad O., Alreshidi, Mousa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161512/
https://www.ncbi.nlm.nih.gov/pubmed/35650591
http://dx.doi.org/10.1186/s12885-022-09567-4
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author Hawsawi, Yousef M.
Shams, Anwar
Theyab, Abdulrahman
Abdali, Wed A.
Hussien, Nahed A.
Alatwi, Hanan E.
Alzahrani, Othman R.
Oyouni, Atif Abdulwahab A.
Babalghith, Ahmad O.
Alreshidi, Mousa
author_facet Hawsawi, Yousef M.
Shams, Anwar
Theyab, Abdulrahman
Abdali, Wed A.
Hussien, Nahed A.
Alatwi, Hanan E.
Alzahrani, Othman R.
Oyouni, Atif Abdulwahab A.
Babalghith, Ahmad O.
Alreshidi, Mousa
author_sort Hawsawi, Yousef M.
collection PubMed
description The full-length BRCA1-associated RING domain 1 (BARD1) gene encodes a 777-aa protein. BARD1 displays a dual role in cancer development and progression as it acts as a tumor suppressor and an oncogene. Structurally, BARD1 has homologous domains to BRCA1 that aid their heterodimer interaction to inhibit the progression of different cancers such as breast and ovarian cancers following the BRCA1-dependant pathway. In addition, BARD1 was shown to be involved in other pathways that are involved in tumor suppression (BRCA1-independent pathway) such as the TP53-dependent apoptotic signaling pathway. However, there are abundant BARD1 isoforms exist that are different from the full-length BARD1 due to nonsense and frameshift mutations, or deletions were found to be associated with susceptibility to various cancers including neuroblastoma, lung, breast, and cervical cancers. This article reviews the spectrum of BARD1 full-length genes and its different isoforms and their anticipated associated risk. Additionally, the study also highlights the role of BARD1 as an oncogene in breast cancer patients and its potential uses as a prognostic/diagnostic biomarker and as a therapeutic target for cancer susceptibility testing and treatment.
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spelling pubmed-91615122022-06-03 BARD1 mystery: tumor suppressors are cancer susceptibility genes Hawsawi, Yousef M. Shams, Anwar Theyab, Abdulrahman Abdali, Wed A. Hussien, Nahed A. Alatwi, Hanan E. Alzahrani, Othman R. Oyouni, Atif Abdulwahab A. Babalghith, Ahmad O. Alreshidi, Mousa BMC Cancer Research The full-length BRCA1-associated RING domain 1 (BARD1) gene encodes a 777-aa protein. BARD1 displays a dual role in cancer development and progression as it acts as a tumor suppressor and an oncogene. Structurally, BARD1 has homologous domains to BRCA1 that aid their heterodimer interaction to inhibit the progression of different cancers such as breast and ovarian cancers following the BRCA1-dependant pathway. In addition, BARD1 was shown to be involved in other pathways that are involved in tumor suppression (BRCA1-independent pathway) such as the TP53-dependent apoptotic signaling pathway. However, there are abundant BARD1 isoforms exist that are different from the full-length BARD1 due to nonsense and frameshift mutations, or deletions were found to be associated with susceptibility to various cancers including neuroblastoma, lung, breast, and cervical cancers. This article reviews the spectrum of BARD1 full-length genes and its different isoforms and their anticipated associated risk. Additionally, the study also highlights the role of BARD1 as an oncogene in breast cancer patients and its potential uses as a prognostic/diagnostic biomarker and as a therapeutic target for cancer susceptibility testing and treatment. BioMed Central 2022-06-01 /pmc/articles/PMC9161512/ /pubmed/35650591 http://dx.doi.org/10.1186/s12885-022-09567-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hawsawi, Yousef M.
Shams, Anwar
Theyab, Abdulrahman
Abdali, Wed A.
Hussien, Nahed A.
Alatwi, Hanan E.
Alzahrani, Othman R.
Oyouni, Atif Abdulwahab A.
Babalghith, Ahmad O.
Alreshidi, Mousa
BARD1 mystery: tumor suppressors are cancer susceptibility genes
title BARD1 mystery: tumor suppressors are cancer susceptibility genes
title_full BARD1 mystery: tumor suppressors are cancer susceptibility genes
title_fullStr BARD1 mystery: tumor suppressors are cancer susceptibility genes
title_full_unstemmed BARD1 mystery: tumor suppressors are cancer susceptibility genes
title_short BARD1 mystery: tumor suppressors are cancer susceptibility genes
title_sort bard1 mystery: tumor suppressors are cancer susceptibility genes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161512/
https://www.ncbi.nlm.nih.gov/pubmed/35650591
http://dx.doi.org/10.1186/s12885-022-09567-4
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