Loading…

Controlled Intracellular Polymerization for Cancer Treatment

Numerous prodrugs have been developed and used for cancer treatments to reduce side effects and promote efficacy. In this work, we have developed a new photoactivatable prodrug system based on intracellular photoinduced electron transfer–reversible addition–fragmentation chain-transfer (PET–RAFT) po...

Full description

Saved in:
Bibliographic Details
Published in:JACS Au 2022-03, Vol.2 (3), p.579-589
Main Authors: Zhang, Yichuan, Gao, Quan, Li, Weishuo, He, Rongkun, Zhu, Liwei, Lian, Qianjin, Wang, Liang, Li, Yang, Bradley, Mark, Geng, Jin
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Request full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33
cites cdi_FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33
container_end_page 589
container_issue 3
container_start_page 579
container_title JACS Au
container_volume 2
creator Zhang, Yichuan
Gao, Quan
Li, Weishuo
He, Rongkun
Zhu, Liwei
Lian, Qianjin
Wang, Liang
Li, Yang
Bradley, Mark
Geng, Jin
description Numerous prodrugs have been developed and used for cancer treatments to reduce side effects and promote efficacy. In this work, we have developed a new photoactivatable prodrug system based on intracellular photoinduced electron transfer–reversible addition–fragmentation chain-transfer (PET–RAFT) polymerization. This unique polymerization process provided a platform for the synthesis of structure-predictable polymers with well-defined structures in living cells. The intracellularly generated poly­(N,N-dimethylacrylamide)­s were found to induce cell cycle arrest, apoptosis, and necroptosis, inhibit cell proliferation, and reduce cancer cell motilities. This polymerization-based “prodrug” system efficiently inhibits tumor growth and metastasis both in vitro and in vivo and will promote the development of targeted and directed cancer chemotherapy.
doi_str_mv 10.1021/jacsau.1c00373
format article
fullrecord <record><control><sourceid>proquest_N~.</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_95b927a9afc041e6989a78267cba3cc4</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_95b927a9afc041e6989a78267cba3cc4</doaj_id><sourcerecordid>2646943595</sourcerecordid><originalsourceid>FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33</originalsourceid><addsrcrecordid>eNp1kUtr3DAUhUVJaUIy2yyLlyEwU70sWxACYehjIJAukrW4kq8nHmQrlexC-uurqSchWXSli3TOJ-kcQs4ZXTHK2ZcduATTijlKRSU-kBOuNFuKisqjN_MxWaS0o5Tykgmq6CdyLMqs51SckKt1GMYYvMem2OQJHHo_eYjFz-Cfe4zdHxi7MBRtiMUaBoexuI8IY4_DeEY-tuATLg7rKXn49vV-_WN5e_d9s765XYLUbFw2VtkWG8YVSlCiltCgbgGFay06rJ3E0jLlmKhcY1taqhqs4lpYW4MGIU7JZuY2AXbmKXY9xGcToDP_NkLcGohj5zwaXVrNq-xqHZUMla41VDVXlbMgnJOZdT2znibbY-Nw_2n_Dvr-ZOgezTb8NrWu9hlmwMUBEMOvCdNo-i7tU4MBw5QMV1JpKUpdZulqlroYUorYvl7DqNk3aOYGzaHBbPj89nGv8pe-suByFmSf2YUpDjn3_9H-AvxIqFY</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2646943595</pqid></control><display><type>article</type><title>Controlled Intracellular Polymerization for Cancer Treatment</title><source>American Chemical Society (ACS) Open Access</source><creator>Zhang, Yichuan ; Gao, Quan ; Li, Weishuo ; He, Rongkun ; Zhu, Liwei ; Lian, Qianjin ; Wang, Liang ; Li, Yang ; Bradley, Mark ; Geng, Jin</creator><creatorcontrib>Zhang, Yichuan ; Gao, Quan ; Li, Weishuo ; He, Rongkun ; Zhu, Liwei ; Lian, Qianjin ; Wang, Liang ; Li, Yang ; Bradley, Mark ; Geng, Jin</creatorcontrib><description>Numerous prodrugs have been developed and used for cancer treatments to reduce side effects and promote efficacy. In this work, we have developed a new photoactivatable prodrug system based on intracellular photoinduced electron transfer–reversible addition–fragmentation chain-transfer (PET–RAFT) polymerization. This unique polymerization process provided a platform for the synthesis of structure-predictable polymers with well-defined structures in living cells. The intracellularly generated poly­(N,N-dimethylacrylamide)­s were found to induce cell cycle arrest, apoptosis, and necroptosis, inhibit cell proliferation, and reduce cancer cell motilities. This polymerization-based “prodrug” system efficiently inhibits tumor growth and metastasis both in vitro and in vivo and will promote the development of targeted and directed cancer chemotherapy.</description><identifier>ISSN: 2691-3704</identifier><identifier>EISSN: 2691-3704</identifier><identifier>DOI: 10.1021/jacsau.1c00373</identifier><identifier>PMID: 35373203</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>JACS Au, 2022-03, Vol.2 (3), p.579-589</ispartof><rights>2022 The Authors. Published by American Chemical Society</rights><rights>2022 The Authors. Published by American Chemical Society.</rights><rights>2022 The Authors. Published by American Chemical Society 2022 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33</citedby><cites>FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33</cites><orcidid>0000-0003-3745-0083 ; 0000-0003-2181-0718 ; 0000-0001-7893-1575 ; 0000-0001-7242-4687</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jacsau.1c00373$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jacsau.1c00373$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27080,27924,27925,53791,53793,56762,56812</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.1021/jacsau.1c00373$$EView_record_in_American_Chemical_Society$$FView_record_in_$$GAmerican_Chemical_Society</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35373203$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yichuan</creatorcontrib><creatorcontrib>Gao, Quan</creatorcontrib><creatorcontrib>Li, Weishuo</creatorcontrib><creatorcontrib>He, Rongkun</creatorcontrib><creatorcontrib>Zhu, Liwei</creatorcontrib><creatorcontrib>Lian, Qianjin</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Li, Yang</creatorcontrib><creatorcontrib>Bradley, Mark</creatorcontrib><creatorcontrib>Geng, Jin</creatorcontrib><title>Controlled Intracellular Polymerization for Cancer Treatment</title><title>JACS Au</title><addtitle>JACS Au</addtitle><description>Numerous prodrugs have been developed and used for cancer treatments to reduce side effects and promote efficacy. In this work, we have developed a new photoactivatable prodrug system based on intracellular photoinduced electron transfer–reversible addition–fragmentation chain-transfer (PET–RAFT) polymerization. This unique polymerization process provided a platform for the synthesis of structure-predictable polymers with well-defined structures in living cells. The intracellularly generated poly­(N,N-dimethylacrylamide)­s were found to induce cell cycle arrest, apoptosis, and necroptosis, inhibit cell proliferation, and reduce cancer cell motilities. This polymerization-based “prodrug” system efficiently inhibits tumor growth and metastasis both in vitro and in vivo and will promote the development of targeted and directed cancer chemotherapy.</description><issn>2691-3704</issn><issn>2691-3704</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1kUtr3DAUhUVJaUIy2yyLlyEwU70sWxACYehjIJAukrW4kq8nHmQrlexC-uurqSchWXSli3TOJ-kcQs4ZXTHK2ZcduATTijlKRSU-kBOuNFuKisqjN_MxWaS0o5Tykgmq6CdyLMqs51SckKt1GMYYvMem2OQJHHo_eYjFz-Cfe4zdHxi7MBRtiMUaBoexuI8IY4_DeEY-tuATLg7rKXn49vV-_WN5e_d9s765XYLUbFw2VtkWG8YVSlCiltCgbgGFay06rJ3E0jLlmKhcY1taqhqs4lpYW4MGIU7JZuY2AXbmKXY9xGcToDP_NkLcGohj5zwaXVrNq-xqHZUMla41VDVXlbMgnJOZdT2znibbY-Nw_2n_Dvr-ZOgezTb8NrWu9hlmwMUBEMOvCdNo-i7tU4MBw5QMV1JpKUpdZulqlroYUorYvl7DqNk3aOYGzaHBbPj89nGv8pe-suByFmSf2YUpDjn3_9H-AvxIqFY</recordid><startdate>20220328</startdate><enddate>20220328</enddate><creator>Zhang, Yichuan</creator><creator>Gao, Quan</creator><creator>Li, Weishuo</creator><creator>He, Rongkun</creator><creator>Zhu, Liwei</creator><creator>Lian, Qianjin</creator><creator>Wang, Liang</creator><creator>Li, Yang</creator><creator>Bradley, Mark</creator><creator>Geng, Jin</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3745-0083</orcidid><orcidid>https://orcid.org/0000-0003-2181-0718</orcidid><orcidid>https://orcid.org/0000-0001-7893-1575</orcidid><orcidid>https://orcid.org/0000-0001-7242-4687</orcidid></search><sort><creationdate>20220328</creationdate><title>Controlled Intracellular Polymerization for Cancer Treatment</title><author>Zhang, Yichuan ; Gao, Quan ; Li, Weishuo ; He, Rongkun ; Zhu, Liwei ; Lian, Qianjin ; Wang, Liang ; Li, Yang ; Bradley, Mark ; Geng, Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yichuan</creatorcontrib><creatorcontrib>Gao, Quan</creatorcontrib><creatorcontrib>Li, Weishuo</creatorcontrib><creatorcontrib>He, Rongkun</creatorcontrib><creatorcontrib>Zhu, Liwei</creatorcontrib><creatorcontrib>Lian, Qianjin</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Li, Yang</creatorcontrib><creatorcontrib>Bradley, Mark</creatorcontrib><creatorcontrib>Geng, Jin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>JACS Au</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Zhang, Yichuan</au><au>Gao, Quan</au><au>Li, Weishuo</au><au>He, Rongkun</au><au>Zhu, Liwei</au><au>Lian, Qianjin</au><au>Wang, Liang</au><au>Li, Yang</au><au>Bradley, Mark</au><au>Geng, Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controlled Intracellular Polymerization for Cancer Treatment</atitle><jtitle>JACS Au</jtitle><addtitle>JACS Au</addtitle><date>2022-03-28</date><risdate>2022</risdate><volume>2</volume><issue>3</issue><spage>579</spage><epage>589</epage><pages>579-589</pages><issn>2691-3704</issn><eissn>2691-3704</eissn><abstract>Numerous prodrugs have been developed and used for cancer treatments to reduce side effects and promote efficacy. In this work, we have developed a new photoactivatable prodrug system based on intracellular photoinduced electron transfer–reversible addition–fragmentation chain-transfer (PET–RAFT) polymerization. This unique polymerization process provided a platform for the synthesis of structure-predictable polymers with well-defined structures in living cells. The intracellularly generated poly­(N,N-dimethylacrylamide)­s were found to induce cell cycle arrest, apoptosis, and necroptosis, inhibit cell proliferation, and reduce cancer cell motilities. This polymerization-based “prodrug” system efficiently inhibits tumor growth and metastasis both in vitro and in vivo and will promote the development of targeted and directed cancer chemotherapy.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>35373203</pmid><doi>10.1021/jacsau.1c00373</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-3745-0083</orcidid><orcidid>https://orcid.org/0000-0003-2181-0718</orcidid><orcidid>https://orcid.org/0000-0001-7893-1575</orcidid><orcidid>https://orcid.org/0000-0001-7242-4687</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier ISSN: 2691-3704
ispartof JACS Au, 2022-03, Vol.2 (3), p.579-589
issn 2691-3704
2691-3704
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_95b927a9afc041e6989a78267cba3cc4
source American Chemical Society (ACS) Open Access
title Controlled Intracellular Polymerization for Cancer Treatment
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T20%3A03%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_N~.&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Controlled%20Intracellular%20Polymerization%20for%20Cancer%20Treatment&rft.jtitle=JACS%20Au&rft.au=Zhang,%20Yichuan&rft.date=2022-03-28&rft.volume=2&rft.issue=3&rft.spage=579&rft.epage=589&rft.pages=579-589&rft.issn=2691-3704&rft.eissn=2691-3704&rft_id=info:doi/10.1021/jacsau.1c00373&rft_dat=%3Cproquest_N~.%3E2646943595%3C/proquest_N~.%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a491t-db6bfed126e4a6384ade9fae3cfbece8c4e5b16c137cdbf0568ab6293bb8a9a33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2646943595&rft_id=info:pmid/35373203&rfr_iscdi=true