Smart Accumulating Dual-Targeting Lipid Envelopes Equipping Oncolytic Adenovirus for Enhancing Cancer Gene Therapeutic Efficacy

溶瘤腺病毒 溶瘤病毒 对偶(语法数字) 癌症 遗传增强 癌症治疗 基因 癌症研究 生物 纳米技术 材料科学 遗传学 文学类 艺术
作者
Yuebin Zhao,Thai Minh Duy Le,JinWoo Hong,Ao Jiao,A‐Rum Yoon,Chae‐Ok Yun
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (41): 27869-27890 被引量:18
标识
DOI:10.1021/acsnano.4c02165
摘要

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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
淡定白羊完成签到,获得积分10
1秒前
爆米花应助Su采纳,获得10
1秒前
1秒前
2秒前
2秒前
3秒前
小蘑菇应助噜噜采纳,获得30
3秒前
碧蓝明雪应助噜噜采纳,获得10
4秒前
思源应助噜噜采纳,获得10
4秒前
完美世界应助111采纳,获得10
6秒前
8秒前
9秒前
jiaojiao发布了新的文献求助10
9秒前
9秒前
fofo完成签到,获得积分10
9秒前
JamesPei应助诚心皮卡丘采纳,获得10
11秒前
orixero应助高挑的冬菱采纳,获得20
11秒前
Ava应助Eve采纳,获得10
11秒前
11秒前
FashionBoy应助李朝富采纳,获得10
12秒前
靓丽芙蓉发布了新的文献求助10
12秒前
无辜的丹雪完成签到 ,获得积分10
14秒前
14秒前
14秒前
薄饼哥丶发布了新的文献求助10
14秒前
jiaojiao完成签到,获得积分20
16秒前
bkagyin应助桃子采纳,获得10
16秒前
16秒前
搞怪冷之完成签到 ,获得积分10
17秒前
科技发布了新的文献求助10
17秒前
18秒前
19秒前
maguodrgon发布了新的文献求助10
19秒前
CC应助种一棵树采纳,获得10
19秒前
丰富寄风完成签到,获得积分20
20秒前
camelots发布了新的文献求助10
20秒前
大个应助科研通管家采纳,获得10
20秒前
科研通AI2S应助科研通管家采纳,获得10
21秒前
感性的鞋垫完成签到,获得积分10
21秒前
prigogin应助科研通管家采纳,获得10
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Autoparametric Resonance in Mechanical Systems 1000
Effects of Two Weeks of Red Light Therapy on Choroidal Thickness and Axial Length in Young Adults 700
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 600
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Rutherford's Vascular Surgery and Endovascular Therapy, 2‑Volume Set, 11th Edition 480
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7665540
求助须知:如何正确求助?哪些是违规求助? 9235468
关于积分的说明 19873813
捐赠科研通 7234686
什么是DOI,文献DOI怎么找? 3283560
关于科研通互助平台的介绍 2442341
邀请新用户注册赠送积分活动 2284608