Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer

•Hyaluronic acid functionalization endows the liposomes to actively target tumor cells.•Honokiol shows great promise in breast cancer therapy, both in vitro and in vivo.•The nano-liposomes enhance anti-metastasis and antitumor efficacies against breast cancer. In an effort to enhance antitumor and a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Carbohydrate polymers 2020-05, Vol.235, p.115981-115981, Article 115981
Hauptverfasser: Wang, Jing, Liu, Dan, Guan, Shuang, Zhu, Wenquan, Fan, Li, Zhang, Qi, Cai, Defu
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 115981
container_issue
container_start_page 115981
container_title Carbohydrate polymers
container_volume 235
creator Wang, Jing
Liu, Dan
Guan, Shuang
Zhu, Wenquan
Fan, Li
Zhang, Qi
Cai, Defu
description •Hyaluronic acid functionalization endows the liposomes to actively target tumor cells.•Honokiol shows great promise in breast cancer therapy, both in vitro and in vivo.•The nano-liposomes enhance anti-metastasis and antitumor efficacies against breast cancer. In an effort to enhance antitumor and anti-metastasis of breast cancer, honokiol (HNK) was encapsulated into hyaluronic acid (HA) modified cationic liposomes (Lip). The prepared HA-Lip-HNK had a spherical shape with a narrow size distribution. The enhanced antitumor efficacy of HA-Lip-HNK was investigated in 4T1 cells in vitro, wherein flow cytometry and confocal microscopy analysis revealed its HA/CD44-mediated greater cellular internalization. As anticipate, the significant cytotoxicity of the HA-Lip-HNK was also observed in 4T1 tumor spheroids. Furthermore, the superior prevention of tumor metastasis by HA-Lip-HNK was verified by in vitro anti-invasion, wound healing and anti-migration assessments, and in vivo bioluminescence imaging in pulmonary metastasis model. Finally, compared with unmodified liposomes, the HA-Lip-HNK exhibited higher tumor accumulation, and achieved a tumor growth inhibition rate of 59.5 %. As a result, the HA-Lip-HNK may serve as a promising tumor-targeted drug delivery strategy for the efficient therapy of metastatic breast cancer.
doi_str_mv 10.1016/j.carbpol.2020.115981
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2370495040</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0144861720301557</els_id><sourcerecordid>2370495040</sourcerecordid><originalsourceid>FETCH-LOGICAL-c365t-34f3e79901c56e7bbc6876ba9fc78a1572e2a25b0e2583113a314e33022ca8283</originalsourceid><addsrcrecordid>eNqFkM1u3CAURlHVqJkmeYRWLLPxlAvGP9lEUZQ0lSJl067RNb5umNowAbvSLPruYTrTbIuQEFfn4xOHsU8g1iCg-rJZW4zdNoxrKWSegW4beMdW0NRtAaos37OVgLIsmgrqU_YxpY3IqwLxgZ0qCVJqgBX787DDcYnBO8vRur6YQu8GRz0f3TakMOHIn4MPv1wYuUcfcmt0FK_4nX9Gb4mjn10x0Ywpb5fyvf87m5cpRE7D4CzaHcef6HyaeRcpk9zus_GcnQw4Jro4nmfsx_3d99uH4vHp67fbm8fCqkrPhSoHRXXbCrC6orrrbNXUVYftYOsGQdeSJErdCZK6UQAKFZSklJDSYiMbdcYuD-9uY3hZKM1mcsnSOKKnsCQjVS3KVotSZFQfUBtDSpEGs41uwrgzIMzevNmYo3mzN28O5nPu87Fi6Sbq31L_VGfg-gBQ_ujvrNAk6yhb6F0kO5s-uP9UvAIEv5jm</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2370495040</pqid></control><display><type>article</type><title>Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer</title><source>Elsevier ScienceDirect Journals</source><creator>Wang, Jing ; Liu, Dan ; Guan, Shuang ; Zhu, Wenquan ; Fan, Li ; Zhang, Qi ; Cai, Defu</creator><creatorcontrib>Wang, Jing ; Liu, Dan ; Guan, Shuang ; Zhu, Wenquan ; Fan, Li ; Zhang, Qi ; Cai, Defu</creatorcontrib><description>•Hyaluronic acid functionalization endows the liposomes to actively target tumor cells.•Honokiol shows great promise in breast cancer therapy, both in vitro and in vivo.•The nano-liposomes enhance anti-metastasis and antitumor efficacies against breast cancer. In an effort to enhance antitumor and anti-metastasis of breast cancer, honokiol (HNK) was encapsulated into hyaluronic acid (HA) modified cationic liposomes (Lip). The prepared HA-Lip-HNK had a spherical shape with a narrow size distribution. The enhanced antitumor efficacy of HA-Lip-HNK was investigated in 4T1 cells in vitro, wherein flow cytometry and confocal microscopy analysis revealed its HA/CD44-mediated greater cellular internalization. As anticipate, the significant cytotoxicity of the HA-Lip-HNK was also observed in 4T1 tumor spheroids. Furthermore, the superior prevention of tumor metastasis by HA-Lip-HNK was verified by in vitro anti-invasion, wound healing and anti-migration assessments, and in vivo bioluminescence imaging in pulmonary metastasis model. Finally, compared with unmodified liposomes, the HA-Lip-HNK exhibited higher tumor accumulation, and achieved a tumor growth inhibition rate of 59.5 %. As a result, the HA-Lip-HNK may serve as a promising tumor-targeted drug delivery strategy for the efficient therapy of metastatic breast cancer.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2020.115981</identifier><identifier>PMID: 32122511</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Breast cancer metastasis ; Honokiol ; Hyaluronic acid ; Liposome ; Tumor targeted therapy</subject><ispartof>Carbohydrate polymers, 2020-05, Vol.235, p.115981-115981, Article 115981</ispartof><rights>2020 Elsevier Ltd</rights><rights>Copyright © 2020 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-34f3e79901c56e7bbc6876ba9fc78a1572e2a25b0e2583113a314e33022ca8283</citedby><cites>FETCH-LOGICAL-c365t-34f3e79901c56e7bbc6876ba9fc78a1572e2a25b0e2583113a314e33022ca8283</cites><orcidid>0000-0001-7673-7859</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0144861720301557$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32122511$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Liu, Dan</creatorcontrib><creatorcontrib>Guan, Shuang</creatorcontrib><creatorcontrib>Zhu, Wenquan</creatorcontrib><creatorcontrib>Fan, Li</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Cai, Defu</creatorcontrib><title>Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>•Hyaluronic acid functionalization endows the liposomes to actively target tumor cells.•Honokiol shows great promise in breast cancer therapy, both in vitro and in vivo.•The nano-liposomes enhance anti-metastasis and antitumor efficacies against breast cancer. In an effort to enhance antitumor and anti-metastasis of breast cancer, honokiol (HNK) was encapsulated into hyaluronic acid (HA) modified cationic liposomes (Lip). The prepared HA-Lip-HNK had a spherical shape with a narrow size distribution. The enhanced antitumor efficacy of HA-Lip-HNK was investigated in 4T1 cells in vitro, wherein flow cytometry and confocal microscopy analysis revealed its HA/CD44-mediated greater cellular internalization. As anticipate, the significant cytotoxicity of the HA-Lip-HNK was also observed in 4T1 tumor spheroids. Furthermore, the superior prevention of tumor metastasis by HA-Lip-HNK was verified by in vitro anti-invasion, wound healing and anti-migration assessments, and in vivo bioluminescence imaging in pulmonary metastasis model. Finally, compared with unmodified liposomes, the HA-Lip-HNK exhibited higher tumor accumulation, and achieved a tumor growth inhibition rate of 59.5 %. As a result, the HA-Lip-HNK may serve as a promising tumor-targeted drug delivery strategy for the efficient therapy of metastatic breast cancer.</description><subject>Breast cancer metastasis</subject><subject>Honokiol</subject><subject>Hyaluronic acid</subject><subject>Liposome</subject><subject>Tumor targeted therapy</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkM1u3CAURlHVqJkmeYRWLLPxlAvGP9lEUZQ0lSJl067RNb5umNowAbvSLPruYTrTbIuQEFfn4xOHsU8g1iCg-rJZW4zdNoxrKWSegW4beMdW0NRtAaos37OVgLIsmgrqU_YxpY3IqwLxgZ0qCVJqgBX787DDcYnBO8vRur6YQu8GRz0f3TakMOHIn4MPv1wYuUcfcmt0FK_4nX9Gb4mjn10x0Ywpb5fyvf87m5cpRE7D4CzaHcef6HyaeRcpk9zus_GcnQw4Jro4nmfsx_3d99uH4vHp67fbm8fCqkrPhSoHRXXbCrC6orrrbNXUVYftYOsGQdeSJErdCZK6UQAKFZSklJDSYiMbdcYuD-9uY3hZKM1mcsnSOKKnsCQjVS3KVotSZFQfUBtDSpEGs41uwrgzIMzevNmYo3mzN28O5nPu87Fi6Sbq31L_VGfg-gBQ_ujvrNAk6yhb6F0kO5s-uP9UvAIEv5jm</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Wang, Jing</creator><creator>Liu, Dan</creator><creator>Guan, Shuang</creator><creator>Zhu, Wenquan</creator><creator>Fan, Li</creator><creator>Zhang, Qi</creator><creator>Cai, Defu</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7673-7859</orcidid></search><sort><creationdate>20200501</creationdate><title>Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer</title><author>Wang, Jing ; Liu, Dan ; Guan, Shuang ; Zhu, Wenquan ; Fan, Li ; Zhang, Qi ; Cai, Defu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-34f3e79901c56e7bbc6876ba9fc78a1572e2a25b0e2583113a314e33022ca8283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Breast cancer metastasis</topic><topic>Honokiol</topic><topic>Hyaluronic acid</topic><topic>Liposome</topic><topic>Tumor targeted therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Liu, Dan</creatorcontrib><creatorcontrib>Guan, Shuang</creatorcontrib><creatorcontrib>Zhu, Wenquan</creatorcontrib><creatorcontrib>Fan, Li</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Cai, Defu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Jing</au><au>Liu, Dan</au><au>Guan, Shuang</au><au>Zhu, Wenquan</au><au>Fan, Li</au><au>Zhang, Qi</au><au>Cai, Defu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2020-05-01</date><risdate>2020</risdate><volume>235</volume><spage>115981</spage><epage>115981</epage><pages>115981-115981</pages><artnum>115981</artnum><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>•Hyaluronic acid functionalization endows the liposomes to actively target tumor cells.•Honokiol shows great promise in breast cancer therapy, both in vitro and in vivo.•The nano-liposomes enhance anti-metastasis and antitumor efficacies against breast cancer. In an effort to enhance antitumor and anti-metastasis of breast cancer, honokiol (HNK) was encapsulated into hyaluronic acid (HA) modified cationic liposomes (Lip). The prepared HA-Lip-HNK had a spherical shape with a narrow size distribution. The enhanced antitumor efficacy of HA-Lip-HNK was investigated in 4T1 cells in vitro, wherein flow cytometry and confocal microscopy analysis revealed its HA/CD44-mediated greater cellular internalization. As anticipate, the significant cytotoxicity of the HA-Lip-HNK was also observed in 4T1 tumor spheroids. Furthermore, the superior prevention of tumor metastasis by HA-Lip-HNK was verified by in vitro anti-invasion, wound healing and anti-migration assessments, and in vivo bioluminescence imaging in pulmonary metastasis model. Finally, compared with unmodified liposomes, the HA-Lip-HNK exhibited higher tumor accumulation, and achieved a tumor growth inhibition rate of 59.5 %. As a result, the HA-Lip-HNK may serve as a promising tumor-targeted drug delivery strategy for the efficient therapy of metastatic breast cancer.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>32122511</pmid><doi>10.1016/j.carbpol.2020.115981</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-7673-7859</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0144-8617
ispartof Carbohydrate polymers, 2020-05, Vol.235, p.115981-115981, Article 115981
issn 0144-8617
1879-1344
language eng
recordid cdi_proquest_miscellaneous_2370495040
source Elsevier ScienceDirect Journals
subjects Breast cancer metastasis
Honokiol
Hyaluronic acid
Liposome
Tumor targeted therapy
title Hyaluronic acid-modified liposomal honokiol nanocarrier: Enhance anti-metastasis and antitumor efficacy against breast cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T14%3A49%3A04IST&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=Hyaluronic%20acid-modified%20liposomal%20honokiol%20nanocarrier:%20Enhance%20anti-metastasis%20and%20antitumor%20efficacy%20against%20breast%20cancer&rft.jtitle=Carbohydrate%20polymers&rft.au=Wang,%20Jing&rft.date=2020-05-01&rft.volume=235&rft.spage=115981&rft.epage=115981&rft.pages=115981-115981&rft.artnum=115981&rft.issn=0144-8617&rft.eissn=1879-1344&rft_id=info:doi/10.1016/j.carbpol.2020.115981&rft_dat=%3Cproquest_cross%3E2370495040%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=2370495040&rft_id=info:pmid/32122511&rft_els_id=S0144861720301557&rfr_iscdi=true