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FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin

FAM46B is a member of the family with sequence similarity 46. Little is known about the expression and functional role(s) of FAM46B in prostate cancer (PC). In this study, the expression of FAM46B expression in The Cancer Genome Atlas, GSE55945, and an independent hospital database was measured by b...

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Autores principales: Liang, Tao, Ye, Xuxiao, Liu, Yuanyuan, Qiu, Xinkai, Li, Zuowei, Tian, Binqiang, Yan, Dongliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288130/
https://www.ncbi.nlm.nih.gov/pubmed/30532005
http://dx.doi.org/10.1038/s12276-018-0184-0
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author Liang, Tao
Ye, Xuxiao
Liu, Yuanyuan
Qiu, Xinkai
Li, Zuowei
Tian, Binqiang
Yan, Dongliang
author_facet Liang, Tao
Ye, Xuxiao
Liu, Yuanyuan
Qiu, Xinkai
Li, Zuowei
Tian, Binqiang
Yan, Dongliang
author_sort Liang, Tao
collection PubMed
description FAM46B is a member of the family with sequence similarity 46. Little is known about the expression and functional role(s) of FAM46B in prostate cancer (PC). In this study, the expression of FAM46B expression in The Cancer Genome Atlas, GSE55945, and an independent hospital database was measured by bioinformatics and real-time PCR analysis. After PC cells were transfected with siRNA or a recombinant vector in the absence or presence of a β-catenin signaling inhibitor (XAV-939), the expression levels of FAM46B, C-myc, Cyclin D1, and β-catenin were measured by western blot and real-time PCR. Cell cycle progression and cell proliferation were measured by flow cytometry and the CCK-8 assay. The effects of FAM46B on tumor growth and protein expression in nude mice with PC tumor xenografts were also measured. Our results showed that FAM46B was downregulated but that β-catenin was upregulated in patients with PC. FAM46B silencing promoted cell proliferation and cell cycle progression in PC, which were abrogated by XAV-939. Moreover, FAM46B overexpression inhibited PC cell cycle progression and cell proliferation in vitro and tumor growth in vivo. FAM46B silencing promoted β-catenin protein expression through the inhibition of β-catenin ubiquitination. Our data clearly show that FAM46B inhibits cell proliferation and cell cycle progression in PC through ubiquitination of β-catenin.
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spelling pubmed-62881302018-12-13 FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin Liang, Tao Ye, Xuxiao Liu, Yuanyuan Qiu, Xinkai Li, Zuowei Tian, Binqiang Yan, Dongliang Exp Mol Med Article FAM46B is a member of the family with sequence similarity 46. Little is known about the expression and functional role(s) of FAM46B in prostate cancer (PC). In this study, the expression of FAM46B expression in The Cancer Genome Atlas, GSE55945, and an independent hospital database was measured by bioinformatics and real-time PCR analysis. After PC cells were transfected with siRNA or a recombinant vector in the absence or presence of a β-catenin signaling inhibitor (XAV-939), the expression levels of FAM46B, C-myc, Cyclin D1, and β-catenin were measured by western blot and real-time PCR. Cell cycle progression and cell proliferation were measured by flow cytometry and the CCK-8 assay. The effects of FAM46B on tumor growth and protein expression in nude mice with PC tumor xenografts were also measured. Our results showed that FAM46B was downregulated but that β-catenin was upregulated in patients with PC. FAM46B silencing promoted cell proliferation and cell cycle progression in PC, which were abrogated by XAV-939. Moreover, FAM46B overexpression inhibited PC cell cycle progression and cell proliferation in vitro and tumor growth in vivo. FAM46B silencing promoted β-catenin protein expression through the inhibition of β-catenin ubiquitination. Our data clearly show that FAM46B inhibits cell proliferation and cell cycle progression in PC through ubiquitination of β-catenin. Nature Publishing Group UK 2018-12-10 /pmc/articles/PMC6288130/ /pubmed/30532005 http://dx.doi.org/10.1038/s12276-018-0184-0 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liang, Tao
Ye, Xuxiao
Liu, Yuanyuan
Qiu, Xinkai
Li, Zuowei
Tian, Binqiang
Yan, Dongliang
FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
title FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
title_full FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
title_fullStr FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
title_full_unstemmed FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
title_short FAM46B inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
title_sort fam46b inhibits cell proliferation and cell cycle progression in prostate cancer through ubiquitination of β-catenin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288130/
https://www.ncbi.nlm.nih.gov/pubmed/30532005
http://dx.doi.org/10.1038/s12276-018-0184-0
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