Tetrahedral-DNA-Nanostructure-Modified Engineered Extracellular Vesicles Enhance Oral Squamous Cell Carcinomas Therapy by Targeting GPX4

细胞外小泡 纳米结构 癌症研究 DNA 材料科学 纳米技术 细胞 小泡 化学 医学 细胞生物学 生物化学 生物
作者
Dianri Wang,Yun Wang,Sicheng Zhang,Xueting Yang,Yan Yang,Teng Han,Yi Luo,Chunyan Shui,Mu Yang,Yunfeng Lin,Chao Li
出处
期刊:ACS Nano [American Chemical Society]
标识
DOI:10.1021/acsnano.5c00674
摘要

Oral squamous cell carcinoma (OSCC) represents a heterogeneous group of malignancies originating from the mucosal lining of the oral cavity. Current treatment modalities primarily involve surgery, chemotherapy, and radiotherapy. Despite the use of multimodal therapy, the 5 year overall survival rate for OSCC remains around 50%, underscoring the need for the development of nontoxic agents with potent antitumor activity. Extracellular vesicles (EVs) are nanoscale, membrane-bound structures that can selectively deliver small molecules, nucleic acids, and proteins to target cells, making them a promising platform for drug delivery in cancer therapy. Strategies to improve the uptake of EVs and enhance the delivery of therapeutic molecules to target cells are critical for advancing precision medicine. Tetrahedral DNA nanostructures (TDNs) have shown significant potential in facilitating drug endocytosis and delivery, as well as improving tissue penetration. In this study, TDN@EVs were conducted by modifying the membrane surface of M1-EVs with TDNs, which demonstrated improved biological stability and drug delivery efficiency compared to unmodified EVs. In vitro and in vivo experiments showed that TDN@EVs significantly inhibited OSCC cell proliferation and migration while promoting apoptosis. TDN@EVs exhibited superior drug penetration properties, further amplifying their antitumor effects. Proteomic analysis identified Hsc70 as the key protein responsible for the antitumor activity of the TDN@EVs. The efficient delivery of Hsc70 into tumor cells by TDN@EVs led to the degradation of GPX4, inducing ferroptosis, mitochondrial stress, and DNA damage in tumor cells. These findings highlight the potential of TDN@EVs as an effective and safe approach for cancer therapy. In conclusion, TDN@EVs present as a promising effective strategy for the targeted delivery of therapeutic agents in OSCC treatment, offering enhanced biological stability, efficient drug delivery, and significant antitumor effects.
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
刚刚
liboshi发布了新的文献求助10
1秒前
2秒前
迟大猫应助yang采纳,获得10
2秒前
qinjiehm完成签到,获得积分10
3秒前
脑洞疼应助GanGanGanGan采纳,获得10
5秒前
斯文败类应助tjfwg采纳,获得10
5秒前
量子星尘发布了新的文献求助10
5秒前
111完成签到,获得积分10
7秒前
hjs发布了新的文献求助10
7秒前
8秒前
周周南发布了新的文献求助100
9秒前
hu发布了新的文献求助10
9秒前
google发布了新的文献求助10
10秒前
失眠听南完成签到,获得积分10
10秒前
10秒前
量子星尘发布了新的文献求助10
10秒前
虫二队长完成签到,获得积分10
11秒前
VERITAS完成签到,获得积分10
11秒前
12秒前
uu发布了新的文献求助20
13秒前
英姑应助七七采纳,获得10
14秒前
15秒前
zz发布了新的文献求助10
15秒前
量子星尘发布了新的文献求助10
16秒前
852应助无情的瑾瑜采纳,获得10
16秒前
彩色一曲关注了科研通微信公众号
17秒前
17秒前
18秒前
xin发布了新的文献求助10
19秒前
20秒前
77完成签到,获得积分10
20秒前
20秒前
领导范儿应助科研通管家采纳,获得10
20秒前
我是老大应助科研通管家采纳,获得10
20秒前
20秒前
领导范儿应助科研通管家采纳,获得10
21秒前
21秒前
今后应助科研通管家采纳,获得30
21秒前
华仔应助科研通管家采纳,获得10
21秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2700
An experimental and analytical investigation on the fatigue behaviour of fuselage riveted lap joints: The significance of the rivet squeeze force, and a comparison of 2024-T3 and Glare 3 1000
Neuromuscular and Electrodiagnostic Medicine Board Review 1000
Statistical Methods for the Social Sciences, Global Edition, 6th edition 600
こんなに痛いのにどうして「なんでもない」と医者にいわれてしまうのでしょうか 510
ALUMINUM STANDARDS AND DATA 500
Walter Gilbert: Selected Works 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3664299
求助须知:如何正确求助?哪些是违规求助? 3224405
关于积分的说明 9757262
捐赠科研通 2934339
什么是DOI,文献DOI怎么找? 1606816
邀请新用户注册赠送积分活动 758829
科研通“疑难数据库(出版商)”最低求助积分说明 735012