Exosomal circCARM1 from spheroids reprograms cell metabolism by regulating PFKFB2 in breast cancer
Cancer stem cells (CSC) are the major obstacle for cancer therapy in clinic. Exosomes are one type of vesicles that containing circular RNA (circRNAs) involved in cell–cell communication. However, the roles of breast CSC (BCSC) exosomes are still unclear, and the purpose of the study was to investig...
Gespeichert in:
Veröffentlicht in: | Oncogene 2022-04, Vol.41 (14), p.2012-2025 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2025 |
---|---|
container_issue | 14 |
container_start_page | 2012 |
container_title | Oncogene |
container_volume | 41 |
creator | Liu, Yonglei Ma, Li Hua, Fanli Min, Zhihui Zhan, Yanxia Zhang, Wei Yao, Junxia |
description | Cancer stem cells (CSC) are the major obstacle for cancer therapy in clinic. Exosomes are one type of vesicles that containing circular RNA (circRNAs) involved in cell–cell communication. However, the roles of breast CSC (BCSC) exosomes are still unclear, and the purpose of the study was to investigate breast cancer cell metabolism reprogramming by circRNAs from BCSC exosomes. The circRNA array was performed in the exosomes secreted from spheroids of MDA-231 cells. circCARM1 was higher in BCSC exosomes than it in the parent breast cancer cells. Further investigation demonstrated that BCSC exosomes circCARM1 played an important role in breast cancer cell glycolysis by miR-1252-5p/PFKFB2. In a conclusion, BCSC exosome-derived circCARM1 played an important role in breast cancer cell glycolysis by sponging miR-1252-5p which regulated PFKFB2 expression. |
doi_str_mv | 10.1038/s41388-021-02061-4 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2620079088</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2646016206</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-3b19cd3c40673893967aec548395f74633ede854323551ed5568b7f45bd9b7b13</originalsourceid><addsrcrecordid>eNp9kU1PGzEQhi1UBCn0D3CoLPXSyxZ_fxxDlBRUEAjRs2V7velGu-tg70rk39cQaCUOHEZzmGfeeTUvAGcY_cCIqvPMMFWqQgSXQgJX7ADMMJOi4lyzT2CGNEeVJpQcg885bxBCUiNyBI4pR0QKoWfALZ9ijr3toG-TX8zvbzBsUuxh3v4JKbZ1hilsU1wn22foQ9fBPozWxa7NPXS7Ml1PnR3bYQ3vVr9WFwS2A3Qp2DxCbwcf0ik4bGyXw5fXfgJ-r5YPi8vq-vbn1WJ-XXkq-VhRh7WvqWdISKo01ULa4DlTVPNGMkFpqIPijBLKOQ4150I52TDuau2kw_QEfN_rFruPU8ij6dv87NgOIU7ZEEFeHqBUQb-9QzdxSkNxVygmEC6oKBTZUz7FnFNozDa1vU07g5F5TsDsEzAlAfOSgGFl6eur9OT6UP9beXt5AegeyGU0rEP6f_sD2b_h2o83</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2646016206</pqid></control><display><type>article</type><title>Exosomal circCARM1 from spheroids reprograms cell metabolism by regulating PFKFB2 in breast cancer</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Liu, Yonglei ; Ma, Li ; Hua, Fanli ; Min, Zhihui ; Zhan, Yanxia ; Zhang, Wei ; Yao, Junxia</creator><creatorcontrib>Liu, Yonglei ; Ma, Li ; Hua, Fanli ; Min, Zhihui ; Zhan, Yanxia ; Zhang, Wei ; Yao, Junxia</creatorcontrib><description>Cancer stem cells (CSC) are the major obstacle for cancer therapy in clinic. Exosomes are one type of vesicles that containing circular RNA (circRNAs) involved in cell–cell communication. However, the roles of breast CSC (BCSC) exosomes are still unclear, and the purpose of the study was to investigate breast cancer cell metabolism reprogramming by circRNAs from BCSC exosomes. The circRNA array was performed in the exosomes secreted from spheroids of MDA-231 cells. circCARM1 was higher in BCSC exosomes than it in the parent breast cancer cells. Further investigation demonstrated that BCSC exosomes circCARM1 played an important role in breast cancer cell glycolysis by miR-1252-5p/PFKFB2. In a conclusion, BCSC exosome-derived circCARM1 played an important role in breast cancer cell glycolysis by sponging miR-1252-5p which regulated PFKFB2 expression.</description><identifier>ISSN: 0950-9232</identifier><identifier>EISSN: 1476-5594</identifier><identifier>DOI: 10.1038/s41388-021-02061-4</identifier><identifier>PMID: 35027669</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/31 ; 13/89 ; 14/5 ; 14/63 ; 38/1 ; 38/77 ; 38/90 ; 38/91 ; 42/100 ; 42/109 ; 42/34 ; 42/44 ; 45/61 ; 45/90 ; 631/67/2327 ; 631/67/71 ; 64/60 ; 96/106 ; 96/95 ; Apoptosis ; Breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Cell Biology ; Cell interactions ; Cell Line, Tumor ; Cell Movement - genetics ; Circular RNA ; Exosomes ; Exosomes - genetics ; Exosomes - metabolism ; Female ; Glycolysis ; Human Genetics ; Humans ; Internal Medicine ; Medicine ; Medicine & Public Health ; Metabolism ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Oncology ; Phosphofructokinase-2 - metabolism ; Spheroids ; Stem cells</subject><ispartof>Oncogene, 2022-04, Vol.41 (14), p.2012-2025</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2022. corrected publication 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer Nature Limited.</rights><rights>The Author(s), under exclusive licence to Springer Nature Limited 2022. corrected publication 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-3b19cd3c40673893967aec548395f74633ede854323551ed5568b7f45bd9b7b13</citedby><cites>FETCH-LOGICAL-c375t-3b19cd3c40673893967aec548395f74633ede854323551ed5568b7f45bd9b7b13</cites><orcidid>0000-0002-1904-0518</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41388-021-02061-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41388-021-02061-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35027669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yonglei</creatorcontrib><creatorcontrib>Ma, Li</creatorcontrib><creatorcontrib>Hua, Fanli</creatorcontrib><creatorcontrib>Min, Zhihui</creatorcontrib><creatorcontrib>Zhan, Yanxia</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Yao, Junxia</creatorcontrib><title>Exosomal circCARM1 from spheroids reprograms cell metabolism by regulating PFKFB2 in breast cancer</title><title>Oncogene</title><addtitle>Oncogene</addtitle><addtitle>Oncogene</addtitle><description>Cancer stem cells (CSC) are the major obstacle for cancer therapy in clinic. Exosomes are one type of vesicles that containing circular RNA (circRNAs) involved in cell–cell communication. However, the roles of breast CSC (BCSC) exosomes are still unclear, and the purpose of the study was to investigate breast cancer cell metabolism reprogramming by circRNAs from BCSC exosomes. The circRNA array was performed in the exosomes secreted from spheroids of MDA-231 cells. circCARM1 was higher in BCSC exosomes than it in the parent breast cancer cells. Further investigation demonstrated that BCSC exosomes circCARM1 played an important role in breast cancer cell glycolysis by miR-1252-5p/PFKFB2. In a conclusion, BCSC exosome-derived circCARM1 played an important role in breast cancer cell glycolysis by sponging miR-1252-5p which regulated PFKFB2 expression.</description><subject>13/31</subject><subject>13/89</subject><subject>14/5</subject><subject>14/63</subject><subject>38/1</subject><subject>38/77</subject><subject>38/90</subject><subject>38/91</subject><subject>42/100</subject><subject>42/109</subject><subject>42/34</subject><subject>42/44</subject><subject>45/61</subject><subject>45/90</subject><subject>631/67/2327</subject><subject>631/67/71</subject><subject>64/60</subject><subject>96/106</subject><subject>96/95</subject><subject>Apoptosis</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Cell Biology</subject><subject>Cell interactions</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - genetics</subject><subject>Circular RNA</subject><subject>Exosomes</subject><subject>Exosomes - genetics</subject><subject>Exosomes - metabolism</subject><subject>Female</subject><subject>Glycolysis</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolism</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Oncology</subject><subject>Phosphofructokinase-2 - metabolism</subject><subject>Spheroids</subject><subject>Stem cells</subject><issn>0950-9232</issn><issn>1476-5594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><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>eNp9kU1PGzEQhi1UBCn0D3CoLPXSyxZ_fxxDlBRUEAjRs2V7velGu-tg70rk39cQaCUOHEZzmGfeeTUvAGcY_cCIqvPMMFWqQgSXQgJX7ADMMJOi4lyzT2CGNEeVJpQcg885bxBCUiNyBI4pR0QKoWfALZ9ijr3toG-TX8zvbzBsUuxh3v4JKbZ1hilsU1wn22foQ9fBPozWxa7NPXS7Ml1PnR3bYQ3vVr9WFwS2A3Qp2DxCbwcf0ik4bGyXw5fXfgJ-r5YPi8vq-vbn1WJ-XXkq-VhRh7WvqWdISKo01ULa4DlTVPNGMkFpqIPijBLKOQ4150I52TDuau2kw_QEfN_rFruPU8ij6dv87NgOIU7ZEEFeHqBUQb-9QzdxSkNxVygmEC6oKBTZUz7FnFNozDa1vU07g5F5TsDsEzAlAfOSgGFl6eur9OT6UP9beXt5AegeyGU0rEP6f_sD2b_h2o83</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Liu, Yonglei</creator><creator>Ma, Li</creator><creator>Hua, Fanli</creator><creator>Min, Zhihui</creator><creator>Zhan, Yanxia</creator><creator>Zhang, Wei</creator><creator>Yao, Junxia</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</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>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1904-0518</orcidid></search><sort><creationdate>20220401</creationdate><title>Exosomal circCARM1 from spheroids reprograms cell metabolism by regulating PFKFB2 in breast cancer</title><author>Liu, Yonglei ; Ma, Li ; Hua, Fanli ; Min, Zhihui ; Zhan, Yanxia ; Zhang, Wei ; Yao, Junxia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-3b19cd3c40673893967aec548395f74633ede854323551ed5568b7f45bd9b7b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>13/31</topic><topic>13/89</topic><topic>14/5</topic><topic>14/63</topic><topic>38/1</topic><topic>38/77</topic><topic>38/90</topic><topic>38/91</topic><topic>42/100</topic><topic>42/109</topic><topic>42/34</topic><topic>42/44</topic><topic>45/61</topic><topic>45/90</topic><topic>631/67/2327</topic><topic>631/67/71</topic><topic>64/60</topic><topic>96/106</topic><topic>96/95</topic><topic>Apoptosis</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Cell Biology</topic><topic>Cell interactions</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - genetics</topic><topic>Circular RNA</topic><topic>Exosomes</topic><topic>Exosomes - genetics</topic><topic>Exosomes - metabolism</topic><topic>Female</topic><topic>Glycolysis</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolism</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Oncology</topic><topic>Phosphofructokinase-2 - metabolism</topic><topic>Spheroids</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yonglei</creatorcontrib><creatorcontrib>Ma, Li</creatorcontrib><creatorcontrib>Hua, Fanli</creatorcontrib><creatorcontrib>Min, Zhihui</creatorcontrib><creatorcontrib>Zhan, Yanxia</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Yao, Junxia</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>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</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 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>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>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</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 Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Oncogene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yonglei</au><au>Ma, Li</au><au>Hua, Fanli</au><au>Min, Zhihui</au><au>Zhan, Yanxia</au><au>Zhang, Wei</au><au>Yao, Junxia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exosomal circCARM1 from spheroids reprograms cell metabolism by regulating PFKFB2 in breast cancer</atitle><jtitle>Oncogene</jtitle><stitle>Oncogene</stitle><addtitle>Oncogene</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>41</volume><issue>14</issue><spage>2012</spage><epage>2025</epage><pages>2012-2025</pages><issn>0950-9232</issn><eissn>1476-5594</eissn><abstract>Cancer stem cells (CSC) are the major obstacle for cancer therapy in clinic. Exosomes are one type of vesicles that containing circular RNA (circRNAs) involved in cell–cell communication. However, the roles of breast CSC (BCSC) exosomes are still unclear, and the purpose of the study was to investigate breast cancer cell metabolism reprogramming by circRNAs from BCSC exosomes. The circRNA array was performed in the exosomes secreted from spheroids of MDA-231 cells. circCARM1 was higher in BCSC exosomes than it in the parent breast cancer cells. Further investigation demonstrated that BCSC exosomes circCARM1 played an important role in breast cancer cell glycolysis by miR-1252-5p/PFKFB2. In a conclusion, BCSC exosome-derived circCARM1 played an important role in breast cancer cell glycolysis by sponging miR-1252-5p which regulated PFKFB2 expression.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>35027669</pmid><doi>10.1038/s41388-021-02061-4</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1904-0518</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0950-9232 |
ispartof | Oncogene, 2022-04, Vol.41 (14), p.2012-2025 |
issn | 0950-9232 1476-5594 |
language | eng |
recordid | cdi_proquest_miscellaneous_2620079088 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | 13/31 13/89 14/5 14/63 38/1 38/77 38/90 38/91 42/100 42/109 42/34 42/44 45/61 45/90 631/67/2327 631/67/71 64/60 96/106 96/95 Apoptosis Breast cancer Breast Neoplasms - genetics Breast Neoplasms - metabolism Cell Biology Cell interactions Cell Line, Tumor Cell Movement - genetics Circular RNA Exosomes Exosomes - genetics Exosomes - metabolism Female Glycolysis Human Genetics Humans Internal Medicine Medicine Medicine & Public Health Metabolism MicroRNAs - genetics MicroRNAs - metabolism Oncology Phosphofructokinase-2 - metabolism Spheroids Stem cells |
title | Exosomal circCARM1 from spheroids reprograms cell metabolism by regulating PFKFB2 in breast cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T02%3A24%3A14IST&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=Exosomal%20circCARM1%20from%20spheroids%20reprograms%20cell%20metabolism%20by%20regulating%20PFKFB2%20in%20breast%20cancer&rft.jtitle=Oncogene&rft.au=Liu,%20Yonglei&rft.date=2022-04-01&rft.volume=41&rft.issue=14&rft.spage=2012&rft.epage=2025&rft.pages=2012-2025&rft.issn=0950-9232&rft.eissn=1476-5594&rft_id=info:doi/10.1038/s41388-021-02061-4&rft_dat=%3Cproquest_cross%3E2646016206%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=2646016206&rft_id=info:pmid/35027669&rfr_iscdi=true |