Cited 0 time in
Smart Accumulating Dual-Targeting Lipid Envelopes Equipping Oncolytic Adenovirus for Enhancing Cancer Gene Therapeutic Efficacy
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Zhao, Yuebin | - |
| dc.contributor.author | Le, Thai Minh Duy | - |
| dc.contributor.author | Hong, Jinwoo | - |
| dc.contributor.author | Jiao, Ao | - |
| dc.contributor.author | Yoon, A-Rum | - |
| dc.contributor.author | Yun, Chae-Ok | - |
| dc.date.accessioned | 2026-06-05T01:30:26Z | - |
| dc.date.available | 2026-06-05T01:30:26Z | - |
| dc.date.issued | 2024-10 | - |
| dc.identifier.issn | 1936-0851 | - |
| dc.identifier.issn | 1936-086X | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/213028 | - |
| dc.description.abstract | Systemic delivery of oncolytic adenovirus (oAd) for cancer gene therapy must overcome several limitations such as rapid clearance from the blood, nonspecific accumulation in the liver, and insufficient delivery to the tumor tissues. In the present report, a tumor microenvironment-triggered artificial lipid envelope composed of a pH-responsive sulfamethazine-based polymer (PUSSM)-conjugated phospholipid (DOPE-HZ-PUSSM) and another lipid decorated with epidermal growth factor receptor (EGFR) targeting peptide (GE11) (GE11-DOPE) was utilized to encapsulate replication-incompetent Ad (dAd) or oAd coexpressing short-hairpin RNA (shRNA) against Wnt5 (shWnt5) and decorin (dAd/LP-GE-PS or oAd/LP-GE-PS, respectively). In vitro studies demonstrated that dAd/LP-GE-PS transduced breast cancer cells in a pH-responsive and EGFR-specific manner, showing a higher level of transduction than naked Ad under a mildly acidic pH of 6.0 in EGFR-positive cell lines. In vivo biodistribution analyses revealed that systemic administration of oAd/LP-GE-PS leads to a significantly higher level of intratumoral virion accumulation compared to naked oAd, oAd encapsulated in a liposome without PUSSM or EGFR targeting peptide moiety (oAd/LP), or oAd encapsulated in a liposome with EGFR targeting peptide alone (oAd/LP-GE) in an EGFR overexpressing MDA-MB-468 breast tumor xenograft model, showing that both pH sensitivity and EGFR targeting ability were integral to effective systemic delivery of oAd. Further, systemic administration of all liposomal oAd formulations (oAd/LP, oAd/LP-GE, and oAd/LP-GE-PS) showed significantly attenuated hepatic accumulation of the virus compared to naked oAd. Collectively, our findings demonstrated that pH-sensitive and EGFR-targeted liposomal systemic delivery of oAd can be a promising strategy to address the conventional limitations of oAd to effectively treat EGFR-positive cancer in a safe manner. | - |
| dc.format.extent | 22 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | AMER CHEMICAL SOC | - |
| dc.title | Smart Accumulating Dual-Targeting Lipid Envelopes Equipping Oncolytic Adenovirus for Enhancing Cancer Gene Therapeutic Efficacy | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acsnano.4c02165 | - |
| dc.identifier.scopusid | 2-s2.0-85205677215 | - |
| dc.identifier.wosid | 001327129700001 | - |
| dc.identifier.bibliographicCitation | ACS NANO, v.18, no.41, pp 27869 - 27890 | - |
| dc.citation.title | ACS NANO | - |
| dc.citation.volume | 18 | - |
| dc.citation.number | 41 | - |
| dc.citation.startPage | 27869 | - |
| dc.citation.endPage | 27890 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | GROWTH-FACTOR-RECEPTOR | - |
| dc.subject.keywordPlus | CRITICAL MICELLE CONCENTRATION | - |
| dc.subject.keywordPlus | BREAST-CANCER | - |
| dc.subject.keywordPlus | IN-VITRO | - |
| dc.subject.keywordPlus | REPLICATION-COMPETENT | - |
| dc.subject.keywordPlus | SYSTEMIC DELIVERY | - |
| dc.subject.keywordPlus | TUMOR-METASTASIS | - |
| dc.subject.keywordPlus | LIPOSOMES | - |
| dc.subject.keywordPlus | PH | - |
| dc.subject.keywordPlus | NANOPARTICLES | - |
| dc.subject.keywordAuthor | liposome | - |
| dc.subject.keywordAuthor | pH sensitive | - |
| dc.subject.keywordAuthor | epidermalgrowth factorreceptor (EGFR) | - |
| dc.subject.keywordAuthor | oncolytic adenovirus | - |
| dc.subject.keywordAuthor | gene therapy | - |
| dc.subject.keywordAuthor | nanoplatform | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/acsnano.4c02165 | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1366
COPYRIGHT © 2024 HANYANG UNIVERSITY.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.
