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The importance of CDC27 in cancer: molecular pathology and clinical aspects

BACKGROUND: CDC27 is one of the core components of Anaphase Promoting complex/cyclosome. The main role of this protein is defined at cellular division to control cell cycle transitions. Here we review the molecular aspects that may affect CDC27 regulation from cell cycle and mitosis to cancer pathog...

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Autores principales: Kazemi-Sefat, Golnaz Ensieh, Keramatipour, Mohammad, Talebi, Saeed, Kavousi, Kaveh, Sajed, Roya, Kazemi-Sefat, Nazanin Atieh, Mousavizadeh, Kazem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941923/
https://www.ncbi.nlm.nih.gov/pubmed/33750395
http://dx.doi.org/10.1186/s12935-021-01860-9
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author Kazemi-Sefat, Golnaz Ensieh
Keramatipour, Mohammad
Talebi, Saeed
Kavousi, Kaveh
Sajed, Roya
Kazemi-Sefat, Nazanin Atieh
Mousavizadeh, Kazem
author_facet Kazemi-Sefat, Golnaz Ensieh
Keramatipour, Mohammad
Talebi, Saeed
Kavousi, Kaveh
Sajed, Roya
Kazemi-Sefat, Nazanin Atieh
Mousavizadeh, Kazem
author_sort Kazemi-Sefat, Golnaz Ensieh
collection PubMed
description BACKGROUND: CDC27 is one of the core components of Anaphase Promoting complex/cyclosome. The main role of this protein is defined at cellular division to control cell cycle transitions. Here we review the molecular aspects that may affect CDC27 regulation from cell cycle and mitosis to cancer pathogenesis and prognosis. MAIN TEXT: It has been suggested that CDC27 may play either like a tumor suppressor gene or oncogene in different neoplasms. Divergent variations in CDC27 DNA sequence and alterations in transcription of CDC27 have been detected in different solid tumors and hematological malignancies. Elevated CDC27 expression level may increase cell proliferation, invasiveness and metastasis in some malignancies. It has been proposed that CDC27 upregulation may increase stemness in cancer stem cells. On the other hand, downregulation of CDC27 may increase the cancer cell survival, decrease radiosensitivity and increase chemoresistancy. In addition, CDC27 downregulation may stimulate efferocytosis and improve tumor microenvironment. CONCLUSION: CDC27 dysregulation, either increased or decreased activity, may aggravate neoplasms. CDC27 may be suggested as a prognostic biomarker in different malignancies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-01860-9.
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spelling pubmed-79419232021-03-09 The importance of CDC27 in cancer: molecular pathology and clinical aspects Kazemi-Sefat, Golnaz Ensieh Keramatipour, Mohammad Talebi, Saeed Kavousi, Kaveh Sajed, Roya Kazemi-Sefat, Nazanin Atieh Mousavizadeh, Kazem Cancer Cell Int Review BACKGROUND: CDC27 is one of the core components of Anaphase Promoting complex/cyclosome. The main role of this protein is defined at cellular division to control cell cycle transitions. Here we review the molecular aspects that may affect CDC27 regulation from cell cycle and mitosis to cancer pathogenesis and prognosis. MAIN TEXT: It has been suggested that CDC27 may play either like a tumor suppressor gene or oncogene in different neoplasms. Divergent variations in CDC27 DNA sequence and alterations in transcription of CDC27 have been detected in different solid tumors and hematological malignancies. Elevated CDC27 expression level may increase cell proliferation, invasiveness and metastasis in some malignancies. It has been proposed that CDC27 upregulation may increase stemness in cancer stem cells. On the other hand, downregulation of CDC27 may increase the cancer cell survival, decrease radiosensitivity and increase chemoresistancy. In addition, CDC27 downregulation may stimulate efferocytosis and improve tumor microenvironment. CONCLUSION: CDC27 dysregulation, either increased or decreased activity, may aggravate neoplasms. CDC27 may be suggested as a prognostic biomarker in different malignancies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-01860-9. BioMed Central 2021-03-09 /pmc/articles/PMC7941923/ /pubmed/33750395 http://dx.doi.org/10.1186/s12935-021-01860-9 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Kazemi-Sefat, Golnaz Ensieh
Keramatipour, Mohammad
Talebi, Saeed
Kavousi, Kaveh
Sajed, Roya
Kazemi-Sefat, Nazanin Atieh
Mousavizadeh, Kazem
The importance of CDC27 in cancer: molecular pathology and clinical aspects
title The importance of CDC27 in cancer: molecular pathology and clinical aspects
title_full The importance of CDC27 in cancer: molecular pathology and clinical aspects
title_fullStr The importance of CDC27 in cancer: molecular pathology and clinical aspects
title_full_unstemmed The importance of CDC27 in cancer: molecular pathology and clinical aspects
title_short The importance of CDC27 in cancer: molecular pathology and clinical aspects
title_sort importance of cdc27 in cancer: molecular pathology and clinical aspects
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941923/
https://www.ncbi.nlm.nih.gov/pubmed/33750395
http://dx.doi.org/10.1186/s12935-021-01860-9
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