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Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis
Cell cycle is one of the main cellular mechanisms involved in tumor progression. Almost all of the active molecular pathways in tumor cells directly or indirectly target the cell cycle progression. Therefore, it is necessary to assess the molecular mechanisms involved in cell cycle regulation in tum...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808980/ https://www.ncbi.nlm.nih.gov/pubmed/36597150 http://dx.doi.org/10.1186/s40659-022-00411-4 |
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author | Zangouei, Amir Sadra Zangoue, Malihe Taghehchian, Negin Zangooie, Alireza Rahimi, Hamid Reza Saburi, Ehsan Alavi, Mahya Sadat Moghbeli, Meysam |
author_facet | Zangouei, Amir Sadra Zangoue, Malihe Taghehchian, Negin Zangooie, Alireza Rahimi, Hamid Reza Saburi, Ehsan Alavi, Mahya Sadat Moghbeli, Meysam |
author_sort | Zangouei, Amir Sadra |
collection | PubMed |
description | Cell cycle is one of the main cellular mechanisms involved in tumor progression. Almost all of the active molecular pathways in tumor cells directly or indirectly target the cell cycle progression. Therefore, it is necessary to assess the molecular mechanisms involved in cell cycle regulation in tumor cells. Since, early diagnosis has pivotal role in better cancer management and treatment, it is required to introduce the non-invasive diagnostic markers. Long non-coding RNAs (LncRNAs) have higher stability in body fluids in comparison with mRNAs. Therefore, they can be used as efficient non-invasive markers for the early detection of breast cancer (BCa). In the present review we have summarized all of the reported lncRNAs involved in cell cycle regulation in BCa. It has been reported that lncRNAs mainly affect the cell cycle in G1/S transition through the CCND1/CDK4-6 complex. Present review paves the way of introducing the cell cycle related lncRNAs as efficient markers for the early detection of BCa. |
format | Online Article Text |
id | pubmed-9808980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98089802023-01-04 Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis Zangouei, Amir Sadra Zangoue, Malihe Taghehchian, Negin Zangooie, Alireza Rahimi, Hamid Reza Saburi, Ehsan Alavi, Mahya Sadat Moghbeli, Meysam Biol Res Review Cell cycle is one of the main cellular mechanisms involved in tumor progression. Almost all of the active molecular pathways in tumor cells directly or indirectly target the cell cycle progression. Therefore, it is necessary to assess the molecular mechanisms involved in cell cycle regulation in tumor cells. Since, early diagnosis has pivotal role in better cancer management and treatment, it is required to introduce the non-invasive diagnostic markers. Long non-coding RNAs (LncRNAs) have higher stability in body fluids in comparison with mRNAs. Therefore, they can be used as efficient non-invasive markers for the early detection of breast cancer (BCa). In the present review we have summarized all of the reported lncRNAs involved in cell cycle regulation in BCa. It has been reported that lncRNAs mainly affect the cell cycle in G1/S transition through the CCND1/CDK4-6 complex. Present review paves the way of introducing the cell cycle related lncRNAs as efficient markers for the early detection of BCa. BioMed Central 2023-01-03 /pmc/articles/PMC9808980/ /pubmed/36597150 http://dx.doi.org/10.1186/s40659-022-00411-4 Text en © The Author(s) 2023 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 | Review Zangouei, Amir Sadra Zangoue, Malihe Taghehchian, Negin Zangooie, Alireza Rahimi, Hamid Reza Saburi, Ehsan Alavi, Mahya Sadat Moghbeli, Meysam Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis |
title | Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis |
title_full | Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis |
title_fullStr | Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis |
title_full_unstemmed | Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis |
title_short | Cell cycle related long non-coding RNAs as the critical regulators of breast cancer progression and metastasis |
title_sort | cell cycle related long non-coding rnas as the critical regulators of breast cancer progression and metastasis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808980/ https://www.ncbi.nlm.nih.gov/pubmed/36597150 http://dx.doi.org/10.1186/s40659-022-00411-4 |
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