Cargando…
FBXW7 in Cancer: What Has Been Unraveled Thus Far?
The FBXW7 (F-box with 7 tandem WD40) protein encoded by the gene FBXW7 is one of the crucial components of ubiquitin ligase called Skp1-Cullin1-F-box (SCF) complex that aids in the degradation of many oncoproteins via the ubiquitin-proteasome system (UPS) thus regulating cellular growth. FBXW7 is co...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406609/ https://www.ncbi.nlm.nih.gov/pubmed/30791487 http://dx.doi.org/10.3390/cancers11020246 |
_version_ | 1783401352368488448 |
---|---|
author | Sailo, Bethsebie Lalduhsaki Banik, Kishore Girisa, Sosmitha Bordoloi, Devivasha Fan, Lu Halim, Clarissa Esmeralda Wang, Hong Kumar, Alan Prem Zheng, Dali Mao, Xinliang Sethi, Gautam Kunnumakkara, Ajaikumar Bahulayan |
author_facet | Sailo, Bethsebie Lalduhsaki Banik, Kishore Girisa, Sosmitha Bordoloi, Devivasha Fan, Lu Halim, Clarissa Esmeralda Wang, Hong Kumar, Alan Prem Zheng, Dali Mao, Xinliang Sethi, Gautam Kunnumakkara, Ajaikumar Bahulayan |
author_sort | Sailo, Bethsebie Lalduhsaki |
collection | PubMed |
description | The FBXW7 (F-box with 7 tandem WD40) protein encoded by the gene FBXW7 is one of the crucial components of ubiquitin ligase called Skp1-Cullin1-F-box (SCF) complex that aids in the degradation of many oncoproteins via the ubiquitin-proteasome system (UPS) thus regulating cellular growth. FBXW7 is considered as a potent tumor suppressor as most of its target substrates can function as potential growth promoters, including c-Myc, Notch, cyclin E, c-JUN, and KLF5. Its regulators include p53, C/EBP-δ, Numb, microRNAs, Pin 1, Hes-5, BMI1, Ebp2. Mounting evidence has indicated the involvement of aberrant expression of FBXW7 for tumorigenesis. Moreover, numerous studies have also shown its role in cancer cell chemosensitization, thereby demonstrating the importance of FBXW7 in the development of curative cancer therapy. This comprehensive review emphasizes on the targets, functions, regulators and expression of FBXW7 in different cancers and its involvement in sensitizing cancer cells to chemotherapeutic drugs. |
format | Online Article Text |
id | pubmed-6406609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64066092019-03-21 FBXW7 in Cancer: What Has Been Unraveled Thus Far? Sailo, Bethsebie Lalduhsaki Banik, Kishore Girisa, Sosmitha Bordoloi, Devivasha Fan, Lu Halim, Clarissa Esmeralda Wang, Hong Kumar, Alan Prem Zheng, Dali Mao, Xinliang Sethi, Gautam Kunnumakkara, Ajaikumar Bahulayan Cancers (Basel) Review The FBXW7 (F-box with 7 tandem WD40) protein encoded by the gene FBXW7 is one of the crucial components of ubiquitin ligase called Skp1-Cullin1-F-box (SCF) complex that aids in the degradation of many oncoproteins via the ubiquitin-proteasome system (UPS) thus regulating cellular growth. FBXW7 is considered as a potent tumor suppressor as most of its target substrates can function as potential growth promoters, including c-Myc, Notch, cyclin E, c-JUN, and KLF5. Its regulators include p53, C/EBP-δ, Numb, microRNAs, Pin 1, Hes-5, BMI1, Ebp2. Mounting evidence has indicated the involvement of aberrant expression of FBXW7 for tumorigenesis. Moreover, numerous studies have also shown its role in cancer cell chemosensitization, thereby demonstrating the importance of FBXW7 in the development of curative cancer therapy. This comprehensive review emphasizes on the targets, functions, regulators and expression of FBXW7 in different cancers and its involvement in sensitizing cancer cells to chemotherapeutic drugs. MDPI 2019-02-19 /pmc/articles/PMC6406609/ /pubmed/30791487 http://dx.doi.org/10.3390/cancers11020246 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Sailo, Bethsebie Lalduhsaki Banik, Kishore Girisa, Sosmitha Bordoloi, Devivasha Fan, Lu Halim, Clarissa Esmeralda Wang, Hong Kumar, Alan Prem Zheng, Dali Mao, Xinliang Sethi, Gautam Kunnumakkara, Ajaikumar Bahulayan FBXW7 in Cancer: What Has Been Unraveled Thus Far? |
title | FBXW7 in Cancer: What Has Been Unraveled Thus Far? |
title_full | FBXW7 in Cancer: What Has Been Unraveled Thus Far? |
title_fullStr | FBXW7 in Cancer: What Has Been Unraveled Thus Far? |
title_full_unstemmed | FBXW7 in Cancer: What Has Been Unraveled Thus Far? |
title_short | FBXW7 in Cancer: What Has Been Unraveled Thus Far? |
title_sort | fbxw7 in cancer: what has been unraveled thus far? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406609/ https://www.ncbi.nlm.nih.gov/pubmed/30791487 http://dx.doi.org/10.3390/cancers11020246 |
work_keys_str_mv | AT sailobethsebielalduhsaki fbxw7incancerwhathasbeenunraveledthusfar AT banikkishore fbxw7incancerwhathasbeenunraveledthusfar AT girisasosmitha fbxw7incancerwhathasbeenunraveledthusfar AT bordoloidevivasha fbxw7incancerwhathasbeenunraveledthusfar AT fanlu fbxw7incancerwhathasbeenunraveledthusfar AT halimclarissaesmeralda fbxw7incancerwhathasbeenunraveledthusfar AT wanghong fbxw7incancerwhathasbeenunraveledthusfar AT kumaralanprem fbxw7incancerwhathasbeenunraveledthusfar AT zhengdali fbxw7incancerwhathasbeenunraveledthusfar AT maoxinliang fbxw7incancerwhathasbeenunraveledthusfar AT sethigautam fbxw7incancerwhathasbeenunraveledthusfar AT kunnumakkaraajaikumarbahulayan fbxw7incancerwhathasbeenunraveledthusfar |