Nanomedicine‐boosting icaritin-based immunotherapy of advanced hepatocellular carcinoma

dc.bibliographicCitation.firstPage69
dc.bibliographicCitation.issue1
dc.bibliographicCitation.journalTitleMilitary Medical Researcheng
dc.bibliographicCitation.volume9
dc.contributor.authorLu, Yi
dc.contributor.authorGao, Yue
dc.contributor.authorYang, Huan
dc.contributor.authorHu, Yong
dc.contributor.authorLi, Xin
dc.date.accessioned2023-02-06T10:22:45Z
dc.date.available2023-02-06T10:22:45Z
dc.date.issued2022
dc.description.abstractTraditional treatments for advanced hepatocellular carcinoma (HCC), such as surgical resection, transplantation, radiofrequency ablation, and chemotherapy are unsatisfactory, and therefore the exploration of powerful therapeutic strategies is urgently needed. Immunotherapy has emerged as a promising strategy for advanced HCC treatment due to its minimal side effects and long-lasting therapeutic memory effects. Recent studies have demonstrated that icaritin could serve as an immunomodulator for effective immunotherapy of advanced HCC. Encouragingly, in 2022, icaritin soft capsules were approved by the National Medical Products Administration (NMPA) of China for the immunotherapy of advanced HCC. However, the therapeutic efficacy of icaritin in clinical practice is impaired by its poor bioavailability and unfavorable in vivo delivery efficiency. Recently, functionalized drug delivery systems including stimuli-responsive nanocarriers, cell membrane-coated nanocarriers, and living cell-nanocarrier systems have been designed to overcome the shortcomings of drugs, including the low bioavailability and limited delivery efficiency as well as side effects. Taken together, the development of icaritin-based nanomedicines is expected to further improve the immunotherapy of advanced HCC. Herein, we compared the different preparation methods for icaritin, interpreted the HCC immune microenvironment and the mechanisms underlying icaritin for treatment of advanced HCC, and discussed both the design of icaritin-based nanomedicines with high icaritin loading and the latest progress in icaritin-based nanomedicines for advanced HCC immunotherapy. Finally, the prospects to promote further clinical translation of icaritin-based nanomedicines for the immunotherapy of advanced HCC were proposed.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/11281
dc.identifier.urihttp://dx.doi.org/10.34657/10317
dc.language.isoeng
dc.publisherLondon : BioMed Central
dc.relation.doihttps://doi.org/10.1186/s40779-022-00433-9
dc.relation.essn2054-9369
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc610
dc.subject.otherAdvanced hepatocellular carcinomaeng
dc.subject.otherClinical translationeng
dc.subject.otherIcaritineng
dc.subject.otherImmunotherapyeng
dc.subject.otherNanomedicineeng
dc.titleNanomedicine‐boosting icaritin-based immunotherapy of advanced hepatocellular carcinomaeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorDWI
wgl.subjectMedizin, Gesundheitger
wgl.typeZeitschriftenartikelger
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