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FBW7 in hematological tumors

F-box and WD repeat domain-containing protein 7 (FBW7), also known as FBXW7, AGO or hCDC4, is an F-box protein with seven tandem WD40 repeats. FBW7 is a key substrate recognition subunit of the Skp1-Cul1-F-box-protein E3 ubiquitin ligase. FBW7 targets for ubiquitination and destruction of numerous c...

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Autores principales: Zhu, Qiaojuan, Hu, Linjun, Guo, Yang, Xiao, Zunqiang, Xu, Qiuran, Tong, Xiangmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039162/
https://www.ncbi.nlm.nih.gov/pubmed/32194657
http://dx.doi.org/10.3892/ol.2020.11264
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author Zhu, Qiaojuan
Hu, Linjun
Guo, Yang
Xiao, Zunqiang
Xu, Qiuran
Tong, Xiangmin
author_facet Zhu, Qiaojuan
Hu, Linjun
Guo, Yang
Xiao, Zunqiang
Xu, Qiuran
Tong, Xiangmin
author_sort Zhu, Qiaojuan
collection PubMed
description F-box and WD repeat domain-containing protein 7 (FBW7), also known as FBXW7, AGO or hCDC4, is an F-box protein with seven tandem WD40 repeats. FBW7 is a key substrate recognition subunit of the Skp1-Cul1-F-box-protein E3 ubiquitin ligase. FBW7 targets for ubiquitination and destruction of numerous crucial transcription factors and protooncogenes, including cyclin E, c-Myc, c-Jun, Notch and MCL-1. FBW7 is a well-characterized tumor suppressor, and its gene is frequently mutated or deleted in various types of human cancer, including colorectal cancer, gastric cancer, ovarian cancer and different types of leukemia. Accumulating evidence indicates that the aberrant expression of FBW7 is involved in the development of hematological tumors, including T cell acute lymphoblastic leukemia, adult T cell leukemia/lymphoma, chronic lymphocytic leukemia and multiple myeloma. The present review will describe the latest findings on the role of FBW7 in hematological tumors, in order to identify a novel target for future therapies.
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spelling pubmed-70391622020-03-19 FBW7 in hematological tumors Zhu, Qiaojuan Hu, Linjun Guo, Yang Xiao, Zunqiang Xu, Qiuran Tong, Xiangmin Oncol Lett Review F-box and WD repeat domain-containing protein 7 (FBW7), also known as FBXW7, AGO or hCDC4, is an F-box protein with seven tandem WD40 repeats. FBW7 is a key substrate recognition subunit of the Skp1-Cul1-F-box-protein E3 ubiquitin ligase. FBW7 targets for ubiquitination and destruction of numerous crucial transcription factors and protooncogenes, including cyclin E, c-Myc, c-Jun, Notch and MCL-1. FBW7 is a well-characterized tumor suppressor, and its gene is frequently mutated or deleted in various types of human cancer, including colorectal cancer, gastric cancer, ovarian cancer and different types of leukemia. Accumulating evidence indicates that the aberrant expression of FBW7 is involved in the development of hematological tumors, including T cell acute lymphoblastic leukemia, adult T cell leukemia/lymphoma, chronic lymphocytic leukemia and multiple myeloma. The present review will describe the latest findings on the role of FBW7 in hematological tumors, in order to identify a novel target for future therapies. D.A. Spandidos 2020-03 2020-01-08 /pmc/articles/PMC7039162/ /pubmed/32194657 http://dx.doi.org/10.3892/ol.2020.11264 Text en Copyright: © Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Zhu, Qiaojuan
Hu, Linjun
Guo, Yang
Xiao, Zunqiang
Xu, Qiuran
Tong, Xiangmin
FBW7 in hematological tumors
title FBW7 in hematological tumors
title_full FBW7 in hematological tumors
title_fullStr FBW7 in hematological tumors
title_full_unstemmed FBW7 in hematological tumors
title_short FBW7 in hematological tumors
title_sort fbw7 in hematological tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039162/
https://www.ncbi.nlm.nih.gov/pubmed/32194657
http://dx.doi.org/10.3892/ol.2020.11264
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