Cytoplasmic Clusterin Suppresses Lung Cancer Metastasis by Inhibiting the ROCK1-ERK Axis
Clusterin (CLU) is a heterodimeric glycoprotein that has been detected in diverse human tissues and implicated in many cellular processes. Accumulating evidence indicates that the expression of secreted CLU correlates with the progression of cancers. However, the molecular mechanisms underlying its...
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Veröffentlicht in: | Cancers 2022-05, Vol.14 (10), p.2463 |
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description | Clusterin (CLU) is a heterodimeric glycoprotein that has been detected in diverse human tissues and implicated in many cellular processes. Accumulating evidence indicates that the expression of secreted CLU correlates with the progression of cancers. However, the molecular mechanisms underlying its tumor-suppressive roles are incompletely uncovered. In this study, we demonstrate that precursor CLU is widely downregulated in lung cancer tissue, in which secretory CLU proteins are slightly decreased. Impressively, overexpressing CLU potently inhibits the migration, invasion and metastasis of lung cancer cells, whereas silencing CLU promotes this behavior; however, it appears that secretory CLU fails to exert similar anti-metastatic effects. Interestingly, the cytoplasmic precursor CLU binds ROCK1 to abrogate the interaction between ROCK1 and ERK and impair ERK activity, leading to the suppression of lung cancer invasiveness. Meanwhile, the expression of CLU was remarkably diminished in lung cancer bone metastasis loci when compared with subcutaneous tumors in the mouse model and hardly detected in the bone metastasis loci of lung cancer patients when compared with the primary. These findings reveal a novel insight into the function and regulation of cytoplasmic CLU in lung cancer, which might be a potential target for the diagnosis and treatment of metastatic lung cancer. |
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Accumulating evidence indicates that the expression of secreted CLU correlates with the progression of cancers. However, the molecular mechanisms underlying its tumor-suppressive roles are incompletely uncovered. In this study, we demonstrate that precursor CLU is widely downregulated in lung cancer tissue, in which secretory CLU proteins are slightly decreased. Impressively, overexpressing CLU potently inhibits the migration, invasion and metastasis of lung cancer cells, whereas silencing CLU promotes this behavior; however, it appears that secretory CLU fails to exert similar anti-metastatic effects. Interestingly, the cytoplasmic precursor CLU binds ROCK1 to abrogate the interaction between ROCK1 and ERK and impair ERK activity, leading to the suppression of lung cancer invasiveness. Meanwhile, the expression of CLU was remarkably diminished in lung cancer bone metastasis loci when compared with subcutaneous tumors in the mouse model and hardly detected in the bone metastasis loci of lung cancer patients when compared with the primary. These findings reveal a novel insight into the function and regulation of cytoplasmic CLU in lung cancer, which might be a potential target for the diagnosis and treatment of metastatic lung cancer.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers14102463</identifier><identifier>PMID: 35626071</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antibodies ; Apoptosis ; Bone cancer ; Bone tumors ; Breast cancer ; Cancer therapies ; Cell adhesion & migration ; Cell cycle ; Cell migration ; Clusterin ; Diagnosis ; Extracellular signal-regulated kinase ; Invasiveness ; Kinases ; Lung cancer ; Metastases ; Metastasis ; Molecular modelling ; Phosphorylation ; Proteins</subject><ispartof>Cancers, 2022-05, Vol.14 (10), p.2463</ispartof><rights>2022 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 (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-8c794d2069a03429146e32a9bd98c559f1324ce7cc1e0ad6e6eacf24390f3fff3</citedby><cites>FETCH-LOGICAL-c421t-8c794d2069a03429146e32a9bd98c559f1324ce7cc1e0ad6e6eacf24390f3fff3</cites><orcidid>0000-0003-1973-5552 ; 0000-0001-8777-1657</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140019/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140019/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35626071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Shaobo</creatorcontrib><creatorcontrib>Li, Xu</creatorcontrib><creatorcontrib>Gu, Weiqi</creatorcontrib><creatorcontrib>Li, Xiaoyi</creatorcontrib><creatorcontrib>Zhao, Jingjing</creatorcontrib><creatorcontrib>Wu, Jueheng</creatorcontrib><creatorcontrib>Cai, Junchao</creatorcontrib><creatorcontrib>Feng, Xianming</creatorcontrib><creatorcontrib>Tao, Tianyu</creatorcontrib><title>Cytoplasmic Clusterin Suppresses Lung Cancer Metastasis by Inhibiting the ROCK1-ERK Axis</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Clusterin (CLU) is a heterodimeric glycoprotein that has been detected in diverse human tissues and implicated in many cellular processes. Accumulating evidence indicates that the expression of secreted CLU correlates with the progression of cancers. However, the molecular mechanisms underlying its tumor-suppressive roles are incompletely uncovered. In this study, we demonstrate that precursor CLU is widely downregulated in lung cancer tissue, in which secretory CLU proteins are slightly decreased. Impressively, overexpressing CLU potently inhibits the migration, invasion and metastasis of lung cancer cells, whereas silencing CLU promotes this behavior; however, it appears that secretory CLU fails to exert similar anti-metastatic effects. Interestingly, the cytoplasmic precursor CLU binds ROCK1 to abrogate the interaction between ROCK1 and ERK and impair ERK activity, leading to the suppression of lung cancer invasiveness. Meanwhile, the expression of CLU was remarkably diminished in lung cancer bone metastasis loci when compared with subcutaneous tumors in the mouse model and hardly detected in the bone metastasis loci of lung cancer patients when compared with the primary. These findings reveal a novel insight into the function and regulation of cytoplasmic CLU in lung cancer, which might be a potential target for the diagnosis and treatment of metastatic lung cancer.</description><subject>Antibodies</subject><subject>Apoptosis</subject><subject>Bone cancer</subject><subject>Bone tumors</subject><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Cell adhesion & migration</subject><subject>Cell cycle</subject><subject>Cell migration</subject><subject>Clusterin</subject><subject>Diagnosis</subject><subject>Extracellular signal-regulated kinase</subject><subject>Invasiveness</subject><subject>Kinases</subject><subject>Lung cancer</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Molecular modelling</subject><subject>Phosphorylation</subject><subject>Proteins</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkdFLHDEQxoNYVKzPfSsBX3zZmklyiXkpyKJVvCLYFvoWcrlZL7K3u2Z2pfffG6sVawhkYH75Zj4-xj6B-KKUE8cxdBEzgQYhtVFbbE8KKytjnN5-U--yA6I7UY5SYI3dYbtqZqQRFvbY73oz9kMbaJ0ir9uJRsyp4z-mYchIhMTnU3fL67-j-HccA5WbiC82_LJbpUUaU-mPK-Q31_UVVGc3V_z0T6KP7EMTWsKDl3ef_To_-1lfVPPrb5f16byKWsJYnUTr9FIK44JQWjrQBpUMbrF0J3E2cw0oqSPaGAFFWBo0GGIjdfHfqKZp1D77-qw7TIs1LiN2Yw6tH3Jah7zxfUj-_06XVv62f_BllBDgisDRi0Du7yek0a8TRWzb0GE_kZfGgrQKAAp6-A6966fcFXtPlAABYEWhjp-pmHuijM3rMiD8U3D-XXDlx-e3Hl75fzGpR8molQM</recordid><startdate>20220517</startdate><enddate>20220517</enddate><creator>Huang, Shaobo</creator><creator>Li, Xu</creator><creator>Gu, Weiqi</creator><creator>Li, Xiaoyi</creator><creator>Zhao, Jingjing</creator><creator>Wu, Jueheng</creator><creator>Cai, Junchao</creator><creator>Feng, Xianming</creator><creator>Tao, Tianyu</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1973-5552</orcidid><orcidid>https://orcid.org/0000-0001-8777-1657</orcidid></search><sort><creationdate>20220517</creationdate><title>Cytoplasmic Clusterin Suppresses Lung Cancer Metastasis by Inhibiting the ROCK1-ERK Axis</title><author>Huang, Shaobo ; Li, Xu ; Gu, Weiqi ; Li, Xiaoyi ; Zhao, Jingjing ; Wu, Jueheng ; Cai, Junchao ; Feng, Xianming ; Tao, Tianyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-8c794d2069a03429146e32a9bd98c559f1324ce7cc1e0ad6e6eacf24390f3fff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies</topic><topic>Apoptosis</topic><topic>Bone cancer</topic><topic>Bone tumors</topic><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Cell adhesion & migration</topic><topic>Cell cycle</topic><topic>Cell migration</topic><topic>Clusterin</topic><topic>Diagnosis</topic><topic>Extracellular signal-regulated kinase</topic><topic>Invasiveness</topic><topic>Kinases</topic><topic>Lung cancer</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Molecular modelling</topic><topic>Phosphorylation</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Shaobo</creatorcontrib><creatorcontrib>Li, Xu</creatorcontrib><creatorcontrib>Gu, Weiqi</creatorcontrib><creatorcontrib>Li, Xiaoyi</creatorcontrib><creatorcontrib>Zhao, Jingjing</creatorcontrib><creatorcontrib>Wu, Jueheng</creatorcontrib><creatorcontrib>Cai, Junchao</creatorcontrib><creatorcontrib>Feng, Xianming</creatorcontrib><creatorcontrib>Tao, Tianyu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Shaobo</au><au>Li, Xu</au><au>Gu, Weiqi</au><au>Li, Xiaoyi</au><au>Zhao, Jingjing</au><au>Wu, Jueheng</au><au>Cai, Junchao</au><au>Feng, Xianming</au><au>Tao, Tianyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytoplasmic Clusterin Suppresses Lung Cancer Metastasis by Inhibiting the ROCK1-ERK Axis</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2022-05-17</date><risdate>2022</risdate><volume>14</volume><issue>10</issue><spage>2463</spage><pages>2463-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Clusterin (CLU) is a heterodimeric glycoprotein that has been detected in diverse human tissues and implicated in many cellular processes. Accumulating evidence indicates that the expression of secreted CLU correlates with the progression of cancers. However, the molecular mechanisms underlying its tumor-suppressive roles are incompletely uncovered. In this study, we demonstrate that precursor CLU is widely downregulated in lung cancer tissue, in which secretory CLU proteins are slightly decreased. Impressively, overexpressing CLU potently inhibits the migration, invasion and metastasis of lung cancer cells, whereas silencing CLU promotes this behavior; however, it appears that secretory CLU fails to exert similar anti-metastatic effects. Interestingly, the cytoplasmic precursor CLU binds ROCK1 to abrogate the interaction between ROCK1 and ERK and impair ERK activity, leading to the suppression of lung cancer invasiveness. Meanwhile, the expression of CLU was remarkably diminished in lung cancer bone metastasis loci when compared with subcutaneous tumors in the mouse model and hardly detected in the bone metastasis loci of lung cancer patients when compared with the primary. These findings reveal a novel insight into the function and regulation of cytoplasmic CLU in lung cancer, which might be a potential target for the diagnosis and treatment of metastatic lung cancer.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35626071</pmid><doi>10.3390/cancers14102463</doi><orcidid>https://orcid.org/0000-0003-1973-5552</orcidid><orcidid>https://orcid.org/0000-0001-8777-1657</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Apoptosis Bone cancer Bone tumors Breast cancer Cancer therapies Cell adhesion & migration Cell cycle Cell migration Clusterin Diagnosis Extracellular signal-regulated kinase Invasiveness Kinases Lung cancer Metastases Metastasis Molecular modelling Phosphorylation Proteins |
title | Cytoplasmic Clusterin Suppresses Lung Cancer Metastasis by Inhibiting the ROCK1-ERK Axis |
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