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N-myc downstream regulated gene 1(NDRG1) promotes the stem-like properties of lung cancer cells through stabilized c-Myc

Abstract Tumor-initiating cells (TICs) play an important role in tumorigenesis and development for many various tissue origin cancers including non-small cell lung cancer (NSCLC). However, the mechani s m to maintain TICs in NSCLC is still largely unknown. Here, we evaluated differences of mRNA expr...

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Published in:Cancer letters 2017-08, Vol.401, p.53-62
Main Authors: Wang, Yongfang, Zhou, You, Tao, Feng, Chai, Shoujie, Xu, Xia, Yang, Ying, Yang, Yiming, Xu, Haiyan, Wang, Kai
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cited_by cdi_FETCH-LOGICAL-c511t-b6fb63c87d5713bae11d761618d0e0b345ef6824eaeecf041d6f283d1b2d90263
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container_title Cancer letters
container_volume 401
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description Abstract Tumor-initiating cells (TICs) play an important role in tumorigenesis and development for many various tissue origin cancers including non-small cell lung cancer (NSCLC). However, the mechani s m to maintain TICs in NSCLC is still largely unknown. Here, we evaluated differences of mRNA expression between parental and oncosphere cells that enriched TICs. We found that N-myc downstream regulated gene 1(NDRG1) was upregulated in oncosphere cells derived from human NSCLC cell lines and primary NSCLC cells. NDRG1 promoted stem-like properties of LTICs in NSCLC including iPSC (induced pluripotent stem cell) factors ( OCT4, SOX2, KLF4, and C-MYC ), the spheres-forming ability and the tumorigenicity of NSCLC. NDRG1 prevented the degradation of c-Myc through Skp2-mediated ubiquitination. NDRG1 directly interacted with Skp2, and decreased phosphorylation of Skp2 through inactivation of CDK2. Finally, we confirmed that NDRG1 was negatively correlated with survival and prognosis. Thus, our findings indicate that NDRG1 is a potential target for eradicating TICs in NSCLC.
doi_str_mv 10.1016/j.canlet.2017.04.031
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However, the mechani s m to maintain TICs in NSCLC is still largely unknown. Here, we evaluated differences of mRNA expression between parental and oncosphere cells that enriched TICs. We found that N-myc downstream regulated gene 1(NDRG1) was upregulated in oncosphere cells derived from human NSCLC cell lines and primary NSCLC cells. NDRG1 promoted stem-like properties of LTICs in NSCLC including iPSC (induced pluripotent stem cell) factors ( OCT4, SOX2, KLF4, and C-MYC ), the spheres-forming ability and the tumorigenicity of NSCLC. NDRG1 prevented the degradation of c-Myc through Skp2-mediated ubiquitination. NDRG1 directly interacted with Skp2, and decreased phosphorylation of Skp2 through inactivation of CDK2. Finally, we confirmed that NDRG1 was negatively correlated with survival and prognosis. Thus, our findings indicate that NDRG1 is a potential target for eradicating TICs in NSCLC.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2017.04.031</identifier><identifier>PMID: 28456659</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>A549 Cells ; Adult ; Aged ; Breast cancer ; c-Myc ; c-Myc protein ; Cancer initiating cells ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - metabolism ; Carcinoma, Non-Small-Cell Lung - mortality ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell cycle ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Cyclin-dependent kinase 2 ; Cyclin-Dependent Kinase 2 - metabolism ; Degradation ; Enrichment ; Female ; Gene expression ; Gene Expression Regulation, Neoplastic ; Genes ; Genomics ; Hematology, Oncology and Palliative Medicine ; Humans ; Inactivation ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Kidney cancer ; Kinases ; KLF4 protein ; Laboratory animals ; Lung cancer ; Lung Neoplasms - genetics ; Lung Neoplasms - metabolism ; Lung Neoplasms - mortality ; Lung Neoplasms - pathology ; Male ; Metastasis ; Middle Aged ; Mortality ; Myc protein ; NDRG1 ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Non-small cell lung carcinoma ; Oct-4 protein ; Phenotype ; Phosphorylation ; Pluripotency ; Polymerase chain reaction ; Prognosis ; Protein Stability ; Proteins ; Proteolysis ; Proto-Oncogene Proteins c-myc - genetics ; Proto-Oncogene Proteins c-myc - metabolism ; RNA Interference ; S-Phase Kinase-Associated Proteins - metabolism ; Signal Transduction ; Skp2 ; Skp2 protein ; Spheroids, Cellular ; Stem cells ; Survival ; Survival Analysis ; Transfection ; Tumor Cells, Cultured ; Tumorigenesis ; Tumorigenicity ; Tumors ; Ubiquitination</subject><ispartof>Cancer letters, 2017-08, Vol.401, p.53-62</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Limited Aug 10, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-b6fb63c87d5713bae11d761618d0e0b345ef6824eaeecf041d6f283d1b2d90263</citedby><cites>FETCH-LOGICAL-c511t-b6fb63c87d5713bae11d761618d0e0b345ef6824eaeecf041d6f283d1b2d90263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28456659$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yongfang</creatorcontrib><creatorcontrib>Zhou, You</creatorcontrib><creatorcontrib>Tao, Feng</creatorcontrib><creatorcontrib>Chai, Shoujie</creatorcontrib><creatorcontrib>Xu, Xia</creatorcontrib><creatorcontrib>Yang, Ying</creatorcontrib><creatorcontrib>Yang, Yiming</creatorcontrib><creatorcontrib>Xu, Haiyan</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><title>N-myc downstream regulated gene 1(NDRG1) promotes the stem-like properties of lung cancer cells through stabilized c-Myc</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Abstract Tumor-initiating cells (TICs) play an important role in tumorigenesis and development for many various tissue origin cancers including non-small cell lung cancer (NSCLC). However, the mechani s m to maintain TICs in NSCLC is still largely unknown. Here, we evaluated differences of mRNA expression between parental and oncosphere cells that enriched TICs. We found that N-myc downstream regulated gene 1(NDRG1) was upregulated in oncosphere cells derived from human NSCLC cell lines and primary NSCLC cells. NDRG1 promoted stem-like properties of LTICs in NSCLC including iPSC (induced pluripotent stem cell) factors ( OCT4, SOX2, KLF4, and C-MYC ), the spheres-forming ability and the tumorigenicity of NSCLC. NDRG1 prevented the degradation of c-Myc through Skp2-mediated ubiquitination. NDRG1 directly interacted with Skp2, and decreased phosphorylation of Skp2 through inactivation of CDK2. Finally, we confirmed that NDRG1 was negatively correlated with survival and prognosis. Thus, our findings indicate that NDRG1 is a potential target for eradicating TICs in NSCLC.</description><subject>A549 Cells</subject><subject>Adult</subject><subject>Aged</subject><subject>Breast cancer</subject><subject>c-Myc</subject><subject>c-Myc protein</subject><subject>Cancer initiating cells</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - mortality</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell cycle</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cyclin-dependent kinase 2</subject><subject>Cyclin-Dependent Kinase 2 - metabolism</subject><subject>Degradation</subject><subject>Enrichment</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes</subject><subject>Genomics</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Inactivation</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Kidney cancer</subject><subject>Kinases</subject><subject>KLF4 protein</subject><subject>Laboratory animals</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Myc protein</subject><subject>NDRG1</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Non-small cell lung carcinoma</subject><subject>Oct-4 protein</subject><subject>Phenotype</subject><subject>Phosphorylation</subject><subject>Pluripotency</subject><subject>Polymerase chain reaction</subject><subject>Prognosis</subject><subject>Protein Stability</subject><subject>Proteins</subject><subject>Proteolysis</subject><subject>Proto-Oncogene Proteins c-myc - genetics</subject><subject>Proto-Oncogene Proteins c-myc - metabolism</subject><subject>RNA Interference</subject><subject>S-Phase Kinase-Associated Proteins - metabolism</subject><subject>Signal Transduction</subject><subject>Skp2</subject><subject>Skp2 protein</subject><subject>Spheroids, Cellular</subject><subject>Stem cells</subject><subject>Survival</subject><subject>Survival Analysis</subject><subject>Transfection</subject><subject>Tumor Cells, Cultured</subject><subject>Tumorigenesis</subject><subject>Tumorigenicity</subject><subject>Tumors</subject><subject>Ubiquitination</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFUk1v1DAUtBCILgv_ACFLXMohi1_sOM4FCRUoSKVIfJytxH7ZeuskW9sBll-Poy0g9cLJkj0znjfzCHkKbAMM5MvdxrSjx7QpGdQbJjaMwz2yAlWXRd0odp-sGGei4IpXJ-RRjDvGWCXq6iE5KZWopKyaFfl5WQwHQ-30Y4wpYDvQgNvZtwkt3eKIFE4v33w-hxd0H6ZhShhpukIaEw6Fd9e4XO8xJJcfpp76edzS7MtgoAa9X9BhmrdXmdF2zrtfWdcUHw_mMXnQtz7ik9tzTb69e_v17H1x8en8w9nri8JUAKnoZN9JblRtqxp41yKArSVIUJYh67iosJeqFNgimp4JsLIvFbfQlbZhpeRrcnrUzUZvZoxJDy4u1toRpzlqUA1vZKMyaU2e34HupjmM2Z2GBgByaEJklDiiTJhiDNjrfXBDGw4amF6a0Tt9bEYvzWgmdG4m057dis_dgPYv6U8VGfDqCMCcxneHQUfjMCdpXUCTtJ3c_364K2C8G51p_TUeMP6bRcdSM_1l2Y5lOaDmrGxyVL8BMQm1kQ</recordid><startdate>20170810</startdate><enddate>20170810</enddate><creator>Wang, Yongfang</creator><creator>Zhou, You</creator><creator>Tao, Feng</creator><creator>Chai, Shoujie</creator><creator>Xu, Xia</creator><creator>Yang, Ying</creator><creator>Yang, Yiming</creator><creator>Xu, Haiyan</creator><creator>Wang, Kai</creator><general>Elsevier B.V</general><general>Elsevier Limited</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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20170810</creationdate><title>N-myc downstream regulated gene 1(NDRG1) promotes the stem-like properties of lung cancer cells through stabilized c-Myc</title><author>Wang, Yongfang ; 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However, the mechani s m to maintain TICs in NSCLC is still largely unknown. Here, we evaluated differences of mRNA expression between parental and oncosphere cells that enriched TICs. We found that N-myc downstream regulated gene 1(NDRG1) was upregulated in oncosphere cells derived from human NSCLC cell lines and primary NSCLC cells. NDRG1 promoted stem-like properties of LTICs in NSCLC including iPSC (induced pluripotent stem cell) factors ( OCT4, SOX2, KLF4, and C-MYC ), the spheres-forming ability and the tumorigenicity of NSCLC. NDRG1 prevented the degradation of c-Myc through Skp2-mediated ubiquitination. NDRG1 directly interacted with Skp2, and decreased phosphorylation of Skp2 through inactivation of CDK2. Finally, we confirmed that NDRG1 was negatively correlated with survival and prognosis. 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subjects A549 Cells
Adult
Aged
Breast cancer
c-Myc
c-Myc protein
Cancer initiating cells
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - metabolism
Carcinoma, Non-Small-Cell Lung - mortality
Carcinoma, Non-Small-Cell Lung - pathology
Cell cycle
Cell Cycle Proteins - genetics
Cell Cycle Proteins - metabolism
Cyclin-dependent kinase 2
Cyclin-Dependent Kinase 2 - metabolism
Degradation
Enrichment
Female
Gene expression
Gene Expression Regulation, Neoplastic
Genes
Genomics
Hematology, Oncology and Palliative Medicine
Humans
Inactivation
Intracellular Signaling Peptides and Proteins - genetics
Intracellular Signaling Peptides and Proteins - metabolism
Kidney cancer
Kinases
KLF4 protein
Laboratory animals
Lung cancer
Lung Neoplasms - genetics
Lung Neoplasms - metabolism
Lung Neoplasms - mortality
Lung Neoplasms - pathology
Male
Metastasis
Middle Aged
Mortality
Myc protein
NDRG1
Neoplastic Stem Cells - metabolism
Neoplastic Stem Cells - pathology
Non-small cell lung carcinoma
Oct-4 protein
Phenotype
Phosphorylation
Pluripotency
Polymerase chain reaction
Prognosis
Protein Stability
Proteins
Proteolysis
Proto-Oncogene Proteins c-myc - genetics
Proto-Oncogene Proteins c-myc - metabolism
RNA Interference
S-Phase Kinase-Associated Proteins - metabolism
Signal Transduction
Skp2
Skp2 protein
Spheroids, Cellular
Stem cells
Survival
Survival Analysis
Transfection
Tumor Cells, Cultured
Tumorigenesis
Tumorigenicity
Tumors
Ubiquitination
title N-myc downstream regulated gene 1(NDRG1) promotes the stem-like properties of lung cancer cells through stabilized c-Myc
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