Pleiotropic role of CCR9/CCL25 signaling in adriamycin-induced cardiomyopathy
[Display omitted] •CCR9 and CCL25 levels were increased in myocardial tissues from ADR-injured mice or ADR-injured HL-1 cardiomyocytes.•CCR9/CCL25-mediated signaling machinery mitigated ADR-induced cardiotoxicity through multiple pathological mechanism.•AMPK serves as a cardinal molecule mediating C...
Gespeichert in:
| Veröffentlicht in: | Journal of advanced research 2024-10 |
|---|---|
| Hauptverfasser: | , , , , , , , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | |
|---|---|
| container_issue | |
| container_start_page | |
| container_title | Journal of advanced research |
| container_volume | |
| creator | Wu, Xue Wang, Zheng Liang, Zhenxing Li, Ning Chen, Junmin Liu, Qiong Lei, Wangrui Wu, Xiaopeng Lu, Chenxi Deng, Chao Chen, Ying Wang, Xue Wei, Jinhong Yang, Yang |
| description | [Display omitted]
•CCR9 and CCL25 levels were increased in myocardial tissues from ADR-injured mice or ADR-injured HL-1 cardiomyocytes.•CCR9/CCL25-mediated signaling machinery mitigated ADR-induced cardiotoxicity through multiple pathological mechanism.•AMPK serves as a cardinal molecule mediating CCR9/CCL25 signaling.•Lithospermic acid alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling.
Adriamycin (ADR)-induced cardiomyopathy is a common problem in many cancer survivors. Recently, specific chemokine receptors have garnered interest as therapeutic targets in cardiovascular diseases.
This study aim to report the role of C–C chemokine receptor 9 (CCR9)/C–C chemokine ligand 25 (CCL25) and its therapeutic potential in ADR-induced cardiomyopathy.
Functional gene knockout and overexpression mouse models were utilized to investigate the role of CCR9 against ADR-induced cardiomyopathy. Transcriptome sequencing was also performed to identify the downstream molecular mechanisms of CCR9.
This study revealed that CCR9 and CCL25 levels were increased in mice and HL-1 cells injured by ADR, consistent with the results of patients with heart failure. Both in vivo and in vitro, CCR9 overexpression overtly aggravated cardiac dysfunction, accompanied by decreased AMPK activity and increased mitochondrial dysfunction, fibrosis, oxidative stress, and apoptosis. However, the cardiac harmful effects of ADR were reserved by CCR9 knockdown, as well as CCR9 overexpression aggravated cardiotoxicity were reserved by AMPK agonist GSK621. By constructing different domain-missing CCR9 mutants, we suspected that the △4 region of CCR9 is important for AMPK activity. Furthermore, transcriptome sequencing further illustrated the mechanism of CCR9 overexpression aggravated ADR-induced cardiotoxicity, which was associated with CYP1A1. Finally, lithospermic acid (LA) was screened and alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling, bolstering CCR9-targeted potential clinical application.
These findings present a promising target and drug for treating chemotherapy-induced cardiotoxicity. |
| doi_str_mv | 10.1016/j.jare.2024.10.018 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3120057436</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2090123224004739</els_id><sourcerecordid>3120057436</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1968-3ff1c99cf326c46c99fc7bd1179ad1d1cdd9858eb07b55e80ccd1e21b216d6ca3</originalsourceid><addsrcrecordid>eNp9kM1LAzEQxYMoKrX_gAfZo5etmexnwIssfkFFET2H7GS2puxuatIK_e9NqXp0LjM83nswP8bOgc-AQ3m1nC21p5ngIo_CjEN9wE4FlzwFIfLDvzsTJ2wawpLHyepaAhyzk0zmuair8pQ9vfRk3dq7lcXEu54S1yVN8yqvmmYuiiTYxah7Oy4SOybaeKuHLdoxtaPZIJkEtTfWDVu30uuP7Rk76nQfaPqzJ-z97vateUjnz_ePzc08RZBlnWZdBygldpkoMS_j2WHVGoBKagMG0BhZFzW1vGqLgmqOaIAEtAJKU6LOJuxy37vy7nNDYa0GG5D6Xo_kNkFlIDgvqjwro1XsrehdCJ46tfJ20H6rgKsdSbVUO5JqR3KnRZIxdPHTv2kHMn-RX27RcL03UPzyy5JXAS2NkYj1hGtlnP2v_xsO04Py</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3120057436</pqid></control><display><type>article</type><title>Pleiotropic role of CCR9/CCL25 signaling in adriamycin-induced cardiomyopathy</title><source>DOAJ Directory of Open Access Journals</source><source>Elsevier ScienceDirect Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Wu, Xue ; Wang, Zheng ; Liang, Zhenxing ; Li, Ning ; Chen, Junmin ; Liu, Qiong ; Lei, Wangrui ; Wu, Xiaopeng ; Lu, Chenxi ; Deng, Chao ; Chen, Ying ; Wang, Xue ; Wei, Jinhong ; Yang, Yang</creator><creatorcontrib>Wu, Xue ; Wang, Zheng ; Liang, Zhenxing ; Li, Ning ; Chen, Junmin ; Liu, Qiong ; Lei, Wangrui ; Wu, Xiaopeng ; Lu, Chenxi ; Deng, Chao ; Chen, Ying ; Wang, Xue ; Wei, Jinhong ; Yang, Yang</creatorcontrib><description>[Display omitted]
•CCR9 and CCL25 levels were increased in myocardial tissues from ADR-injured mice or ADR-injured HL-1 cardiomyocytes.•CCR9/CCL25-mediated signaling machinery mitigated ADR-induced cardiotoxicity through multiple pathological mechanism.•AMPK serves as a cardinal molecule mediating CCR9/CCL25 signaling.•Lithospermic acid alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling.
Adriamycin (ADR)-induced cardiomyopathy is a common problem in many cancer survivors. Recently, specific chemokine receptors have garnered interest as therapeutic targets in cardiovascular diseases.
This study aim to report the role of C–C chemokine receptor 9 (CCR9)/C–C chemokine ligand 25 (CCL25) and its therapeutic potential in ADR-induced cardiomyopathy.
Functional gene knockout and overexpression mouse models were utilized to investigate the role of CCR9 against ADR-induced cardiomyopathy. Transcriptome sequencing was also performed to identify the downstream molecular mechanisms of CCR9.
This study revealed that CCR9 and CCL25 levels were increased in mice and HL-1 cells injured by ADR, consistent with the results of patients with heart failure. Both in vivo and in vitro, CCR9 overexpression overtly aggravated cardiac dysfunction, accompanied by decreased AMPK activity and increased mitochondrial dysfunction, fibrosis, oxidative stress, and apoptosis. However, the cardiac harmful effects of ADR were reserved by CCR9 knockdown, as well as CCR9 overexpression aggravated cardiotoxicity were reserved by AMPK agonist GSK621. By constructing different domain-missing CCR9 mutants, we suspected that the △4 region of CCR9 is important for AMPK activity. Furthermore, transcriptome sequencing further illustrated the mechanism of CCR9 overexpression aggravated ADR-induced cardiotoxicity, which was associated with CYP1A1. Finally, lithospermic acid (LA) was screened and alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling, bolstering CCR9-targeted potential clinical application.
These findings present a promising target and drug for treating chemotherapy-induced cardiotoxicity.</description><identifier>ISSN: 2090-1232</identifier><identifier>ISSN: 2090-1224</identifier><identifier>EISSN: 2090-1224</identifier><identifier>DOI: 10.1016/j.jare.2024.10.018</identifier><identifier>PMID: 39442876</identifier><language>eng</language><publisher>Egypt: Elsevier B.V</publisher><subject>Adriamycin ; AMPK ; Cardiotoxicity ; CCR9/CCL25 ; Lithospermic acid</subject><ispartof>Journal of advanced research, 2024-10</ispartof><rights>2024</rights><rights>Copyright © 2024. Production and hosting by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1968-3ff1c99cf326c46c99fc7bd1179ad1d1cdd9858eb07b55e80ccd1e21b216d6ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2090123224004739$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,860,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39442876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Xue</creatorcontrib><creatorcontrib>Wang, Zheng</creatorcontrib><creatorcontrib>Liang, Zhenxing</creatorcontrib><creatorcontrib>Li, Ning</creatorcontrib><creatorcontrib>Chen, Junmin</creatorcontrib><creatorcontrib>Liu, Qiong</creatorcontrib><creatorcontrib>Lei, Wangrui</creatorcontrib><creatorcontrib>Wu, Xiaopeng</creatorcontrib><creatorcontrib>Lu, Chenxi</creatorcontrib><creatorcontrib>Deng, Chao</creatorcontrib><creatorcontrib>Chen, Ying</creatorcontrib><creatorcontrib>Wang, Xue</creatorcontrib><creatorcontrib>Wei, Jinhong</creatorcontrib><creatorcontrib>Yang, Yang</creatorcontrib><title>Pleiotropic role of CCR9/CCL25 signaling in adriamycin-induced cardiomyopathy</title><title>Journal of advanced research</title><addtitle>J Adv Res</addtitle><description>[Display omitted]
•CCR9 and CCL25 levels were increased in myocardial tissues from ADR-injured mice or ADR-injured HL-1 cardiomyocytes.•CCR9/CCL25-mediated signaling machinery mitigated ADR-induced cardiotoxicity through multiple pathological mechanism.•AMPK serves as a cardinal molecule mediating CCR9/CCL25 signaling.•Lithospermic acid alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling.
Adriamycin (ADR)-induced cardiomyopathy is a common problem in many cancer survivors. Recently, specific chemokine receptors have garnered interest as therapeutic targets in cardiovascular diseases.
This study aim to report the role of C–C chemokine receptor 9 (CCR9)/C–C chemokine ligand 25 (CCL25) and its therapeutic potential in ADR-induced cardiomyopathy.
Functional gene knockout and overexpression mouse models were utilized to investigate the role of CCR9 against ADR-induced cardiomyopathy. Transcriptome sequencing was also performed to identify the downstream molecular mechanisms of CCR9.
This study revealed that CCR9 and CCL25 levels were increased in mice and HL-1 cells injured by ADR, consistent with the results of patients with heart failure. Both in vivo and in vitro, CCR9 overexpression overtly aggravated cardiac dysfunction, accompanied by decreased AMPK activity and increased mitochondrial dysfunction, fibrosis, oxidative stress, and apoptosis. However, the cardiac harmful effects of ADR were reserved by CCR9 knockdown, as well as CCR9 overexpression aggravated cardiotoxicity were reserved by AMPK agonist GSK621. By constructing different domain-missing CCR9 mutants, we suspected that the △4 region of CCR9 is important for AMPK activity. Furthermore, transcriptome sequencing further illustrated the mechanism of CCR9 overexpression aggravated ADR-induced cardiotoxicity, which was associated with CYP1A1. Finally, lithospermic acid (LA) was screened and alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling, bolstering CCR9-targeted potential clinical application.
These findings present a promising target and drug for treating chemotherapy-induced cardiotoxicity.</description><subject>Adriamycin</subject><subject>AMPK</subject><subject>Cardiotoxicity</subject><subject>CCR9/CCL25</subject><subject>Lithospermic acid</subject><issn>2090-1232</issn><issn>2090-1224</issn><issn>2090-1224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kM1LAzEQxYMoKrX_gAfZo5etmexnwIssfkFFET2H7GS2puxuatIK_e9NqXp0LjM83nswP8bOgc-AQ3m1nC21p5ngIo_CjEN9wE4FlzwFIfLDvzsTJ2wawpLHyepaAhyzk0zmuair8pQ9vfRk3dq7lcXEu54S1yVN8yqvmmYuiiTYxah7Oy4SOybaeKuHLdoxtaPZIJkEtTfWDVu30uuP7Rk76nQfaPqzJ-z97vateUjnz_ePzc08RZBlnWZdBygldpkoMS_j2WHVGoBKagMG0BhZFzW1vGqLgmqOaIAEtAJKU6LOJuxy37vy7nNDYa0GG5D6Xo_kNkFlIDgvqjwro1XsrehdCJ46tfJ20H6rgKsdSbVUO5JqR3KnRZIxdPHTv2kHMn-RX27RcL03UPzyy5JXAS2NkYj1hGtlnP2v_xsO04Py</recordid><startdate>20241021</startdate><enddate>20241021</enddate><creator>Wu, Xue</creator><creator>Wang, Zheng</creator><creator>Liang, Zhenxing</creator><creator>Li, Ning</creator><creator>Chen, Junmin</creator><creator>Liu, Qiong</creator><creator>Lei, Wangrui</creator><creator>Wu, Xiaopeng</creator><creator>Lu, Chenxi</creator><creator>Deng, Chao</creator><creator>Chen, Ying</creator><creator>Wang, Xue</creator><creator>Wei, Jinhong</creator><creator>Yang, Yang</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20241021</creationdate><title>Pleiotropic role of CCR9/CCL25 signaling in adriamycin-induced cardiomyopathy</title><author>Wu, Xue ; Wang, Zheng ; Liang, Zhenxing ; Li, Ning ; Chen, Junmin ; Liu, Qiong ; Lei, Wangrui ; Wu, Xiaopeng ; Lu, Chenxi ; Deng, Chao ; Chen, Ying ; Wang, Xue ; Wei, Jinhong ; Yang, Yang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1968-3ff1c99cf326c46c99fc7bd1179ad1d1cdd9858eb07b55e80ccd1e21b216d6ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adriamycin</topic><topic>AMPK</topic><topic>Cardiotoxicity</topic><topic>CCR9/CCL25</topic><topic>Lithospermic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Xue</creatorcontrib><creatorcontrib>Wang, Zheng</creatorcontrib><creatorcontrib>Liang, Zhenxing</creatorcontrib><creatorcontrib>Li, Ning</creatorcontrib><creatorcontrib>Chen, Junmin</creatorcontrib><creatorcontrib>Liu, Qiong</creatorcontrib><creatorcontrib>Lei, Wangrui</creatorcontrib><creatorcontrib>Wu, Xiaopeng</creatorcontrib><creatorcontrib>Lu, Chenxi</creatorcontrib><creatorcontrib>Deng, Chao</creatorcontrib><creatorcontrib>Chen, Ying</creatorcontrib><creatorcontrib>Wang, Xue</creatorcontrib><creatorcontrib>Wei, Jinhong</creatorcontrib><creatorcontrib>Yang, Yang</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of advanced research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Xue</au><au>Wang, Zheng</au><au>Liang, Zhenxing</au><au>Li, Ning</au><au>Chen, Junmin</au><au>Liu, Qiong</au><au>Lei, Wangrui</au><au>Wu, Xiaopeng</au><au>Lu, Chenxi</au><au>Deng, Chao</au><au>Chen, Ying</au><au>Wang, Xue</au><au>Wei, Jinhong</au><au>Yang, Yang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pleiotropic role of CCR9/CCL25 signaling in adriamycin-induced cardiomyopathy</atitle><jtitle>Journal of advanced research</jtitle><addtitle>J Adv Res</addtitle><date>2024-10-21</date><risdate>2024</risdate><issn>2090-1232</issn><issn>2090-1224</issn><eissn>2090-1224</eissn><abstract>[Display omitted]
•CCR9 and CCL25 levels were increased in myocardial tissues from ADR-injured mice or ADR-injured HL-1 cardiomyocytes.•CCR9/CCL25-mediated signaling machinery mitigated ADR-induced cardiotoxicity through multiple pathological mechanism.•AMPK serves as a cardinal molecule mediating CCR9/CCL25 signaling.•Lithospermic acid alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling.
Adriamycin (ADR)-induced cardiomyopathy is a common problem in many cancer survivors. Recently, specific chemokine receptors have garnered interest as therapeutic targets in cardiovascular diseases.
This study aim to report the role of C–C chemokine receptor 9 (CCR9)/C–C chemokine ligand 25 (CCL25) and its therapeutic potential in ADR-induced cardiomyopathy.
Functional gene knockout and overexpression mouse models were utilized to investigate the role of CCR9 against ADR-induced cardiomyopathy. Transcriptome sequencing was also performed to identify the downstream molecular mechanisms of CCR9.
This study revealed that CCR9 and CCL25 levels were increased in mice and HL-1 cells injured by ADR, consistent with the results of patients with heart failure. Both in vivo and in vitro, CCR9 overexpression overtly aggravated cardiac dysfunction, accompanied by decreased AMPK activity and increased mitochondrial dysfunction, fibrosis, oxidative stress, and apoptosis. However, the cardiac harmful effects of ADR were reserved by CCR9 knockdown, as well as CCR9 overexpression aggravated cardiotoxicity were reserved by AMPK agonist GSK621. By constructing different domain-missing CCR9 mutants, we suspected that the △4 region of CCR9 is important for AMPK activity. Furthermore, transcriptome sequencing further illustrated the mechanism of CCR9 overexpression aggravated ADR-induced cardiotoxicity, which was associated with CYP1A1. Finally, lithospermic acid (LA) was screened and alleviated ADR-induced cardiotoxicity through regulation of CCR9/CCL25-AMPK signaling, bolstering CCR9-targeted potential clinical application.
These findings present a promising target and drug for treating chemotherapy-induced cardiotoxicity.</abstract><cop>Egypt</cop><pub>Elsevier B.V</pub><pmid>39442876</pmid><doi>10.1016/j.jare.2024.10.018</doi><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 2090-1232 |
| ispartof | Journal of advanced research, 2024-10 |
| issn | 2090-1232 2090-1224 2090-1224 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_3120057436 |
| source | DOAJ Directory of Open Access Journals; Elsevier ScienceDirect Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
| subjects | Adriamycin AMPK Cardiotoxicity CCR9/CCL25 Lithospermic acid |
| title | Pleiotropic role of CCR9/CCL25 signaling in adriamycin-induced cardiomyopathy |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T12%3A03%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pleiotropic%20role%20of%20CCR9/CCL25%20signaling%20in%20adriamycin-induced%20cardiomyopathy&rft.jtitle=Journal%20of%20advanced%20research&rft.au=Wu,%20Xue&rft.date=2024-10-21&rft.issn=2090-1232&rft.eissn=2090-1224&rft_id=info:doi/10.1016/j.jare.2024.10.018&rft_dat=%3Cproquest_cross%3E3120057436%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3120057436&rft_id=info:pmid/39442876&rft_els_id=S2090123224004739&rfr_iscdi=true |