NEDD4L is downregulated in colorectal cancer and inhibits canonical WNT signaling
The NEDD4 family of E3 ubiquitin ligases includes nine members. Each is a modular protein, containing an N-terminal C2 domain for cell localization, two-to-four central WW domains for substrate recognition, and a C-terminal, catalytic HECT domain, which is responsible for catalyzing the ubiquitylati...
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description | The NEDD4 family of E3 ubiquitin ligases includes nine members. Each is a modular protein, containing an N-terminal C2 domain for cell localization, two-to-four central WW domains for substrate recognition, and a C-terminal, catalytic HECT domain, which is responsible for catalyzing the ubiquitylation reaction. Members of this family are known to affect pathways central to the pathogenesis of colorectal cancer, including the WNT, TGFβ, EGFR, and p53 pathways. Recently, NEDD4 mRNA was reported to be overexpressed in colorectal cancer, but tumor stage was not considered in the analysis. Expression of the other family members has not been studied in colorectal cancer. Herein, we determined the expression patterns of all nine NEDD4 family members in 256 patients who presented with disease ranging from premalignant adenoma to stage IV colorectal cancer. NEDD4 mRNA was significantly increased in all stages of colorectal cancer. In contrast, NEDD4L mRNA, the closest homolog to NEDD4, was the most highly downregulated family member, and was significantly downregulated in all tumor stages. We also found NEDD4L protein was significantly decreased by western blotting in colorectal cancer samples compared to adjacent normal mucosa. In addition, NEDD4L, but not catalytically inactive NEDD4L, inhibited canonical WNT signaling at or below the level of β-catenin in vitro. These findings suggest that NEDD4L may play a tumor suppressive role in colorectal cancer, possibly through inhibition of canonical WNT signaling. |
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Each is a modular protein, containing an N-terminal C2 domain for cell localization, two-to-four central WW domains for substrate recognition, and a C-terminal, catalytic HECT domain, which is responsible for catalyzing the ubiquitylation reaction. Members of this family are known to affect pathways central to the pathogenesis of colorectal cancer, including the WNT, TGFβ, EGFR, and p53 pathways. Recently, NEDD4 mRNA was reported to be overexpressed in colorectal cancer, but tumor stage was not considered in the analysis. Expression of the other family members has not been studied in colorectal cancer. Herein, we determined the expression patterns of all nine NEDD4 family members in 256 patients who presented with disease ranging from premalignant adenoma to stage IV colorectal cancer. NEDD4 mRNA was significantly increased in all stages of colorectal cancer. In contrast, NEDD4L mRNA, the closest homolog to NEDD4, was the most highly downregulated family member, and was significantly downregulated in all tumor stages. We also found NEDD4L protein was significantly decreased by western blotting in colorectal cancer samples compared to adjacent normal mucosa. In addition, NEDD4L, but not catalytically inactive NEDD4L, inhibited canonical WNT signaling at or below the level of β-catenin in vitro. These findings suggest that NEDD4L may play a tumor suppressive role in colorectal cancer, possibly through inhibition of canonical WNT signaling.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0081514</identifier><identifier>PMID: 24312311</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adenoma ; Cancer ; Catalysis ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Developmental biology ; Down-Regulation ; Endosomal Sorting Complexes Required for Transport - metabolism ; Epidermal growth factor receptors ; Gene Expression Regulation, Neoplastic ; Genes ; Genomes ; Homology ; Humans ; Localization ; mRNA ; Mucosa ; Mutation ; Nedd4 Ubiquitin Protein Ligases ; p53 Protein ; Pathogenesis ; Pathways ; Patients ; Prostate cancer ; Proteins ; Signal transduction ; Signaling ; Substrates ; Tumor Suppressor Proteins - metabolism ; Tumorigenesis ; Ubiquitin ; Ubiquitin-protein ligase ; Ubiquitin-Protein Ligases - metabolism ; Western blotting ; Wnt protein ; Wnt Signaling Pathway ; β-Catenin</subject><ispartof>PloS one, 2013-11, Vol.8 (11), p.e81514-e81514</ispartof><rights>This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: http://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-b8b89f1898f90365e8011f508a8c4890d8278a664323a462108e33b74a5621973</citedby><cites>FETCH-LOGICAL-c526t-b8b89f1898f90365e8011f508a8c4890d8278a664323a462108e33b74a5621973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842946/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842946/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24312311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Liu, Chunming</contributor><creatorcontrib>Tanksley, Jarred P</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Coffey, Robert J</creatorcontrib><title>NEDD4L is downregulated in colorectal cancer and inhibits canonical WNT signaling</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The NEDD4 family of E3 ubiquitin ligases includes nine members. Each is a modular protein, containing an N-terminal C2 domain for cell localization, two-to-four central WW domains for substrate recognition, and a C-terminal, catalytic HECT domain, which is responsible for catalyzing the ubiquitylation reaction. Members of this family are known to affect pathways central to the pathogenesis of colorectal cancer, including the WNT, TGFβ, EGFR, and p53 pathways. Recently, NEDD4 mRNA was reported to be overexpressed in colorectal cancer, but tumor stage was not considered in the analysis. Expression of the other family members has not been studied in colorectal cancer. Herein, we determined the expression patterns of all nine NEDD4 family members in 256 patients who presented with disease ranging from premalignant adenoma to stage IV colorectal cancer. NEDD4 mRNA was significantly increased in all stages of colorectal cancer. In contrast, NEDD4L mRNA, the closest homolog to NEDD4, was the most highly downregulated family member, and was significantly downregulated in all tumor stages. We also found NEDD4L protein was significantly decreased by western blotting in colorectal cancer samples compared to adjacent normal mucosa. In addition, NEDD4L, but not catalytically inactive NEDD4L, inhibited canonical WNT signaling at or below the level of β-catenin in vitro. These findings suggest that NEDD4L may play a tumor suppressive role in colorectal cancer, possibly through inhibition of canonical WNT signaling.</description><subject>Adenoma</subject><subject>Cancer</subject><subject>Catalysis</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Developmental biology</subject><subject>Down-Regulation</subject><subject>Endosomal Sorting Complexes Required for Transport - metabolism</subject><subject>Epidermal growth factor receptors</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes</subject><subject>Genomes</subject><subject>Homology</subject><subject>Humans</subject><subject>Localization</subject><subject>mRNA</subject><subject>Mucosa</subject><subject>Mutation</subject><subject>Nedd4 Ubiquitin Protein Ligases</subject><subject>p53 Protein</subject><subject>Pathogenesis</subject><subject>Pathways</subject><subject>Patients</subject><subject>Prostate cancer</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Substrates</subject><subject>Tumor Suppressor Proteins - metabolism</subject><subject>Tumorigenesis</subject><subject>Ubiquitin</subject><subject>Ubiquitin-protein ligase</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><subject>Western blotting</subject><subject>Wnt protein</subject><subject>Wnt Signaling Pathway</subject><subject>β-Catenin</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUl1v1DAQjBCIlsI_QBCJF17u8HecF6SqLVDpVIRUxKO1cTapTz77sBMQ_56kl1Yt4sn27szsrDVF8ZqSNeUV_bCNYwrg1_sYcE2IppKKJ8UxrTlbKUb40wf3o-JFzltCJNdKPS-OmOCUcUqPi29XF-fnYlO6XLbxd0jYjx4GbEsXSht9TGgH8KWFYDGVEObGjWvckOdaDM5O3R9X12V2_eTGhf5l8awDn_HVcp4U3z9dXJ99WW2-fr48O92srGRqWDW60XVHda27mnAlURNKO0k0aCt0TVrNKg1KCc44CMUo0ch5UwmQ06Ou-Enx9qC79zGb5TeyoRNWVBOETojLA6KNsDX75HaQ_pgIztwWYuoNpMFZj6bVhEtZiZpLFEIAUIG04rZDbBUgTlofl2ljs8PWYhgS-EeijzvB3Zg-_jJcC1YLNQm8XwRS_DliHszOZYveQ8A43vqWWjGt5s3e_QP9_3bigLIp5pywuzdDiZkTcscyc0LMkpCJ9ubhIveku0jwv_-CtzM</recordid><startdate>20131128</startdate><enddate>20131128</enddate><creator>Tanksley, Jarred P</creator><creator>Chen, Xi</creator><creator>Coffey, Robert J</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20131128</creationdate><title>NEDD4L is downregulated in colorectal cancer and inhibits canonical WNT signaling</title><author>Tanksley, Jarred P ; Chen, Xi ; Coffey, Robert J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-b8b89f1898f90365e8011f508a8c4890d8278a664323a462108e33b74a5621973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenoma</topic><topic>Cancer</topic><topic>Catalysis</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Developmental biology</topic><topic>Down-Regulation</topic><topic>Endosomal Sorting Complexes Required for Transport - metabolism</topic><topic>Epidermal growth factor receptors</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genes</topic><topic>Genomes</topic><topic>Homology</topic><topic>Humans</topic><topic>Localization</topic><topic>mRNA</topic><topic>Mucosa</topic><topic>Mutation</topic><topic>Nedd4 Ubiquitin Protein Ligases</topic><topic>p53 Protein</topic><topic>Pathogenesis</topic><topic>Pathways</topic><topic>Patients</topic><topic>Prostate cancer</topic><topic>Proteins</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Substrates</topic><topic>Tumor Suppressor Proteins - metabolism</topic><topic>Tumorigenesis</topic><topic>Ubiquitin</topic><topic>Ubiquitin-protein ligase</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><topic>Western blotting</topic><topic>Wnt protein</topic><topic>Wnt Signaling Pathway</topic><topic>β-Catenin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tanksley, Jarred P</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Coffey, Robert J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanksley, Jarred P</au><au>Chen, Xi</au><au>Coffey, Robert J</au><au>Liu, Chunming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NEDD4L is downregulated in colorectal cancer and inhibits canonical WNT signaling</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-11-28</date><risdate>2013</risdate><volume>8</volume><issue>11</issue><spage>e81514</spage><epage>e81514</epage><pages>e81514-e81514</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The NEDD4 family of E3 ubiquitin ligases includes nine members. Each is a modular protein, containing an N-terminal C2 domain for cell localization, two-to-four central WW domains for substrate recognition, and a C-terminal, catalytic HECT domain, which is responsible for catalyzing the ubiquitylation reaction. Members of this family are known to affect pathways central to the pathogenesis of colorectal cancer, including the WNT, TGFβ, EGFR, and p53 pathways. Recently, NEDD4 mRNA was reported to be overexpressed in colorectal cancer, but tumor stage was not considered in the analysis. Expression of the other family members has not been studied in colorectal cancer. Herein, we determined the expression patterns of all nine NEDD4 family members in 256 patients who presented with disease ranging from premalignant adenoma to stage IV colorectal cancer. NEDD4 mRNA was significantly increased in all stages of colorectal cancer. In contrast, NEDD4L mRNA, the closest homolog to NEDD4, was the most highly downregulated family member, and was significantly downregulated in all tumor stages. We also found NEDD4L protein was significantly decreased by western blotting in colorectal cancer samples compared to adjacent normal mucosa. In addition, NEDD4L, but not catalytically inactive NEDD4L, inhibited canonical WNT signaling at or below the level of β-catenin in vitro. These findings suggest that NEDD4L may play a tumor suppressive role in colorectal cancer, possibly through inhibition of canonical WNT signaling.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24312311</pmid><doi>10.1371/journal.pone.0081514</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adenoma Cancer Catalysis Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Developmental biology Down-Regulation Endosomal Sorting Complexes Required for Transport - metabolism Epidermal growth factor receptors Gene Expression Regulation, Neoplastic Genes Genomes Homology Humans Localization mRNA Mucosa Mutation Nedd4 Ubiquitin Protein Ligases p53 Protein Pathogenesis Pathways Patients Prostate cancer Proteins Signal transduction Signaling Substrates Tumor Suppressor Proteins - metabolism Tumorigenesis Ubiquitin Ubiquitin-protein ligase Ubiquitin-Protein Ligases - metabolism Western blotting Wnt protein Wnt Signaling Pathway β-Catenin |
title | NEDD4L is downregulated in colorectal cancer and inhibits canonical WNT signaling |
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