Loading…

Effects of icariin and curcumol on autophagy, ferroptosis, and lipid metabolism based on miR‐7/m‐TOR/SREBP1 pathway on prostate cancer

This study aimed to investigate the effects and underlying molecular mechanisms of icariin (ICA) and curcumol on autophagy, ferroptosis, and lipid metabolism in prostate cancer (PCa), in vitro and in vivo. Normal prostate epithelial cells RWPE‐1 and PCa cell lines DU145 and PC‐3 were treated with IC...

Full description

Saved in:
Bibliographic Details
Published in:BioFactors (Oxford) 2023-03, Vol.49 (2), p.438-456
Main Authors: Xu, Wenjing, Ding, Jin, Li, Bonan, Sun, Tiansong, You, Xujun, He, Qinghu, Sheng, Wen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363
cites cdi_FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363
container_end_page 456
container_issue 2
container_start_page 438
container_title BioFactors (Oxford)
container_volume 49
creator Xu, Wenjing
Ding, Jin
Li, Bonan
Sun, Tiansong
You, Xujun
He, Qinghu
Sheng, Wen
description This study aimed to investigate the effects and underlying molecular mechanisms of icariin (ICA) and curcumol on autophagy, ferroptosis, and lipid metabolism in prostate cancer (PCa), in vitro and in vivo. Normal prostate epithelial cells RWPE‐1 and PCa cell lines DU145 and PC‐3 were treated with ICA and curcumol. Ferrostatin‐1 (Fer‐1) or 3‐MA was added to treat DU145 and PC‐3 cells. In addition, we knocked down miR‐7. The mechanism of ICA and curcumol in PCa cells after the knockdown of miR‐7 was verified by in vitro nude mice tumorigenesis experiments. ICA and curcumol had no significant effect on the viability of RWPE‐1 cells, but there was a significant difference between DU145 and PC‐3 cells. After treatment with ICA and curcumol, the proliferation of PCa cells was inhibited, apoptosis, reactive oxygen species (ROS) levels, and miR‐7 expression were increased. The combined treatment of ICA and curcumol had a more significant effect. ICA and curcumol treatment induced autophagy and ferroptosis in PCa cells, and si‐miR‐7 reversed the effects of ICA and curcumol on autophagy and ferroptosis. MiR‐7 targeted mTOR and regulated the expression of the mTOR/SREBP1 pathway in PCa cells. ICA and curcumol may affect the lipid metabolism of PCa cells by affecting SREBP1. In addition, the effects and mechanisms of ICA and curcumol on autophagy, ferroptosis, and lipid metabolism in PCa cells were verified in vivo. ICA and curcumol synergistically regulated the miR‐7/mTOR/SREBP1 pathway to induce autophagy and ferroptosis in PCa cells and affected lipid metabolism.
doi_str_mv 10.1002/biof.1927
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2759957625</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2759957625</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363</originalsourceid><addsrcrecordid>eNp1kMFO4zAQhq0VaCndPfACyEeQCLXjOE6OgMpuJaSuur1HY2cCRkkd7ESoN86ceEaehIQCNy4zGumbf0YfIUecnXPG4pm2rjrneax-kAnPVBxlLON7ZMJyyaM0EeKAHIZwzxgXLMl-kgORykyqVEzI87yq0HSBuopaA97aDYVNSU3vTd-4mrph7jvX3sHt9oxW6L1rOxdsOHvnatvakjbYgXa1DQ3VELActxq7en16UbNmqOvlavZ_Nb_8x2kL3d0jbEei9S500CE1sDHof5H9CuqAvz_6lKyv5-urv9HN8s_i6uImMiKWKtIqyRA1QlYpyUqOuQDAGEQOqTIlYMqExISpFErNVSql4EkOGgRKLVIxJSe72OH8Q4-hKxobDNY1bND1oYiVzPNBTiwH9HSHmuHT4LEqWm8b8NuCs2I0X4zmi9H8wB5_xPa6wfKL_FQ9ALMd8Ghr3H6fVFwultfvkW-L45Di</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2759957625</pqid></control><display><type>article</type><title>Effects of icariin and curcumol on autophagy, ferroptosis, and lipid metabolism based on miR‐7/m‐TOR/SREBP1 pathway on prostate cancer</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Xu, Wenjing ; Ding, Jin ; Li, Bonan ; Sun, Tiansong ; You, Xujun ; He, Qinghu ; Sheng, Wen</creator><creatorcontrib>Xu, Wenjing ; Ding, Jin ; Li, Bonan ; Sun, Tiansong ; You, Xujun ; He, Qinghu ; Sheng, Wen</creatorcontrib><description>This study aimed to investigate the effects and underlying molecular mechanisms of icariin (ICA) and curcumol on autophagy, ferroptosis, and lipid metabolism in prostate cancer (PCa), in vitro and in vivo. Normal prostate epithelial cells RWPE‐1 and PCa cell lines DU145 and PC‐3 were treated with ICA and curcumol. Ferrostatin‐1 (Fer‐1) or 3‐MA was added to treat DU145 and PC‐3 cells. In addition, we knocked down miR‐7. The mechanism of ICA and curcumol in PCa cells after the knockdown of miR‐7 was verified by in vitro nude mice tumorigenesis experiments. ICA and curcumol had no significant effect on the viability of RWPE‐1 cells, but there was a significant difference between DU145 and PC‐3 cells. After treatment with ICA and curcumol, the proliferation of PCa cells was inhibited, apoptosis, reactive oxygen species (ROS) levels, and miR‐7 expression were increased. The combined treatment of ICA and curcumol had a more significant effect. ICA and curcumol treatment induced autophagy and ferroptosis in PCa cells, and si‐miR‐7 reversed the effects of ICA and curcumol on autophagy and ferroptosis. MiR‐7 targeted mTOR and regulated the expression of the mTOR/SREBP1 pathway in PCa cells. ICA and curcumol may affect the lipid metabolism of PCa cells by affecting SREBP1. In addition, the effects and mechanisms of ICA and curcumol on autophagy, ferroptosis, and lipid metabolism in PCa cells were verified in vivo. ICA and curcumol synergistically regulated the miR‐7/mTOR/SREBP1 pathway to induce autophagy and ferroptosis in PCa cells and affected lipid metabolism.</description><identifier>ISSN: 0951-6433</identifier><identifier>EISSN: 1872-8081</identifier><identifier>DOI: 10.1002/biof.1927</identifier><identifier>PMID: 36585763</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Animals ; autophagy ; Autophagy - genetics ; Cell Line, Tumor ; Cell Proliferation ; curcumol ; ferroptosis ; Ferroptosis - genetics ; Humans ; ICA ; Lipid Metabolism - genetics ; Male ; Mice ; Mice, Nude ; MicroRNAs - genetics ; MicroRNAs - metabolism ; prostate cancer ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism ; TOR Serine-Threonine Kinases - metabolism</subject><ispartof>BioFactors (Oxford), 2023-03, Vol.49 (2), p.438-456</ispartof><rights>2022 International Union of Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363</citedby><cites>FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363</cites><orcidid>0000-0003-0838-2720</orcidid></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/36585763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Wenjing</creatorcontrib><creatorcontrib>Ding, Jin</creatorcontrib><creatorcontrib>Li, Bonan</creatorcontrib><creatorcontrib>Sun, Tiansong</creatorcontrib><creatorcontrib>You, Xujun</creatorcontrib><creatorcontrib>He, Qinghu</creatorcontrib><creatorcontrib>Sheng, Wen</creatorcontrib><title>Effects of icariin and curcumol on autophagy, ferroptosis, and lipid metabolism based on miR‐7/m‐TOR/SREBP1 pathway on prostate cancer</title><title>BioFactors (Oxford)</title><addtitle>Biofactors</addtitle><description>This study aimed to investigate the effects and underlying molecular mechanisms of icariin (ICA) and curcumol on autophagy, ferroptosis, and lipid metabolism in prostate cancer (PCa), in vitro and in vivo. Normal prostate epithelial cells RWPE‐1 and PCa cell lines DU145 and PC‐3 were treated with ICA and curcumol. Ferrostatin‐1 (Fer‐1) or 3‐MA was added to treat DU145 and PC‐3 cells. In addition, we knocked down miR‐7. The mechanism of ICA and curcumol in PCa cells after the knockdown of miR‐7 was verified by in vitro nude mice tumorigenesis experiments. ICA and curcumol had no significant effect on the viability of RWPE‐1 cells, but there was a significant difference between DU145 and PC‐3 cells. After treatment with ICA and curcumol, the proliferation of PCa cells was inhibited, apoptosis, reactive oxygen species (ROS) levels, and miR‐7 expression were increased. The combined treatment of ICA and curcumol had a more significant effect. ICA and curcumol treatment induced autophagy and ferroptosis in PCa cells, and si‐miR‐7 reversed the effects of ICA and curcumol on autophagy and ferroptosis. MiR‐7 targeted mTOR and regulated the expression of the mTOR/SREBP1 pathway in PCa cells. ICA and curcumol may affect the lipid metabolism of PCa cells by affecting SREBP1. In addition, the effects and mechanisms of ICA and curcumol on autophagy, ferroptosis, and lipid metabolism in PCa cells were verified in vivo. ICA and curcumol synergistically regulated the miR‐7/mTOR/SREBP1 pathway to induce autophagy and ferroptosis in PCa cells and affected lipid metabolism.</description><subject>Animals</subject><subject>autophagy</subject><subject>Autophagy - genetics</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>curcumol</subject><subject>ferroptosis</subject><subject>Ferroptosis - genetics</subject><subject>Humans</subject><subject>ICA</subject><subject>Lipid Metabolism - genetics</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>prostate cancer</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>TOR Serine-Threonine Kinases - metabolism</subject><issn>0951-6433</issn><issn>1872-8081</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kMFO4zAQhq0VaCndPfACyEeQCLXjOE6OgMpuJaSuur1HY2cCRkkd7ESoN86ceEaehIQCNy4zGumbf0YfIUecnXPG4pm2rjrneax-kAnPVBxlLON7ZMJyyaM0EeKAHIZwzxgXLMl-kgORykyqVEzI87yq0HSBuopaA97aDYVNSU3vTd-4mrph7jvX3sHt9oxW6L1rOxdsOHvnatvakjbYgXa1DQ3VELActxq7en16UbNmqOvlavZ_Nb_8x2kL3d0jbEei9S500CE1sDHof5H9CuqAvz_6lKyv5-urv9HN8s_i6uImMiKWKtIqyRA1QlYpyUqOuQDAGEQOqTIlYMqExISpFErNVSql4EkOGgRKLVIxJSe72OH8Q4-hKxobDNY1bND1oYiVzPNBTiwH9HSHmuHT4LEqWm8b8NuCs2I0X4zmi9H8wB5_xPa6wfKL_FQ9ALMd8Ghr3H6fVFwultfvkW-L45Di</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Xu, Wenjing</creator><creator>Ding, Jin</creator><creator>Li, Bonan</creator><creator>Sun, Tiansong</creator><creator>You, Xujun</creator><creator>He, Qinghu</creator><creator>Sheng, Wen</creator><general>John Wiley &amp; Sons, Inc</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>7X8</scope><orcidid>https://orcid.org/0000-0003-0838-2720</orcidid></search><sort><creationdate>202303</creationdate><title>Effects of icariin and curcumol on autophagy, ferroptosis, and lipid metabolism based on miR‐7/m‐TOR/SREBP1 pathway on prostate cancer</title><author>Xu, Wenjing ; Ding, Jin ; Li, Bonan ; Sun, Tiansong ; You, Xujun ; He, Qinghu ; Sheng, Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>autophagy</topic><topic>Autophagy - genetics</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>curcumol</topic><topic>ferroptosis</topic><topic>Ferroptosis - genetics</topic><topic>Humans</topic><topic>ICA</topic><topic>Lipid Metabolism - genetics</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>prostate cancer</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>TOR Serine-Threonine Kinases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Wenjing</creatorcontrib><creatorcontrib>Ding, Jin</creatorcontrib><creatorcontrib>Li, Bonan</creatorcontrib><creatorcontrib>Sun, Tiansong</creatorcontrib><creatorcontrib>You, Xujun</creatorcontrib><creatorcontrib>He, Qinghu</creatorcontrib><creatorcontrib>Sheng, Wen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>BioFactors (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Wenjing</au><au>Ding, Jin</au><au>Li, Bonan</au><au>Sun, Tiansong</au><au>You, Xujun</au><au>He, Qinghu</au><au>Sheng, Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of icariin and curcumol on autophagy, ferroptosis, and lipid metabolism based on miR‐7/m‐TOR/SREBP1 pathway on prostate cancer</atitle><jtitle>BioFactors (Oxford)</jtitle><addtitle>Biofactors</addtitle><date>2023-03</date><risdate>2023</risdate><volume>49</volume><issue>2</issue><spage>438</spage><epage>456</epage><pages>438-456</pages><issn>0951-6433</issn><eissn>1872-8081</eissn><abstract>This study aimed to investigate the effects and underlying molecular mechanisms of icariin (ICA) and curcumol on autophagy, ferroptosis, and lipid metabolism in prostate cancer (PCa), in vitro and in vivo. Normal prostate epithelial cells RWPE‐1 and PCa cell lines DU145 and PC‐3 were treated with ICA and curcumol. Ferrostatin‐1 (Fer‐1) or 3‐MA was added to treat DU145 and PC‐3 cells. In addition, we knocked down miR‐7. The mechanism of ICA and curcumol in PCa cells after the knockdown of miR‐7 was verified by in vitro nude mice tumorigenesis experiments. ICA and curcumol had no significant effect on the viability of RWPE‐1 cells, but there was a significant difference between DU145 and PC‐3 cells. After treatment with ICA and curcumol, the proliferation of PCa cells was inhibited, apoptosis, reactive oxygen species (ROS) levels, and miR‐7 expression were increased. The combined treatment of ICA and curcumol had a more significant effect. ICA and curcumol treatment induced autophagy and ferroptosis in PCa cells, and si‐miR‐7 reversed the effects of ICA and curcumol on autophagy and ferroptosis. MiR‐7 targeted mTOR and regulated the expression of the mTOR/SREBP1 pathway in PCa cells. ICA and curcumol may affect the lipid metabolism of PCa cells by affecting SREBP1. In addition, the effects and mechanisms of ICA and curcumol on autophagy, ferroptosis, and lipid metabolism in PCa cells were verified in vivo. ICA and curcumol synergistically regulated the miR‐7/mTOR/SREBP1 pathway to induce autophagy and ferroptosis in PCa cells and affected lipid metabolism.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>36585763</pmid><doi>10.1002/biof.1927</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0003-0838-2720</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0951-6433
ispartof BioFactors (Oxford), 2023-03, Vol.49 (2), p.438-456
issn 0951-6433
1872-8081
language eng
recordid cdi_proquest_miscellaneous_2759957625
source Wiley-Blackwell Read & Publish Collection
subjects Animals
autophagy
Autophagy - genetics
Cell Line, Tumor
Cell Proliferation
curcumol
ferroptosis
Ferroptosis - genetics
Humans
ICA
Lipid Metabolism - genetics
Male
Mice
Mice, Nude
MicroRNAs - genetics
MicroRNAs - metabolism
prostate cancer
Prostatic Neoplasms - drug therapy
Prostatic Neoplasms - genetics
Prostatic Neoplasms - metabolism
TOR Serine-Threonine Kinases - metabolism
title Effects of icariin and curcumol on autophagy, ferroptosis, and lipid metabolism based on miR‐7/m‐TOR/SREBP1 pathway on prostate cancer
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T19%3A00%3A55IST&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=Effects%20of%20icariin%20and%20curcumol%20on%20autophagy,%20ferroptosis,%20and%20lipid%20metabolism%20based%20on%20miR%E2%80%907/m%E2%80%90TOR/SREBP1%20pathway%20on%20prostate%20cancer&rft.jtitle=BioFactors%20(Oxford)&rft.au=Xu,%20Wenjing&rft.date=2023-03&rft.volume=49&rft.issue=2&rft.spage=438&rft.epage=456&rft.pages=438-456&rft.issn=0951-6433&rft.eissn=1872-8081&rft_id=info:doi/10.1002/biof.1927&rft_dat=%3Cproquest_cross%3E2759957625%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3257-b748eebea8f750d1e93aae2a39a67cdae6035e4076adb176553149aba3e5b363%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2759957625&rft_id=info:pmid/36585763&rfr_iscdi=true