亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Abstract 1860: Development of novel AXL inhibitor-loaded PLGA nanoparticles for targeted therapy in triple negative breast cancer

三阴性乳腺癌 癌症 乳腺癌 医学 癌症研究 肿瘤科 内科学
作者
Fatma Kazdal,Nermin Kahraman,Bülent Özpolat
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:85 (8_Supplement_1): 1860-1860
标识
DOI:10.1158/1538-7445.am2025-1860
摘要

Triple Negative Breast Cancer (TNBC) is the most aggressive and heterogeneous subtype of breast cancer with the highest mortality rates. TNBC is characterized by a lack of Estrogen (ER), PR, and HER2 receptors and currently, there is no effective targeted therapy for TNBC patients. AXL, a receptor tyrosine kinase (AXL-RTK), is overexpressed in TNBC cells and patient tumors and has been linked to poor prognosis. Despite its potential as a therapeutic target, there are currently no FDA-approved inhibitors for AXL in TNBC. In this study, we aimed to develop AXL- inhibitor-based targeted therapy and evaluate its therapeutic potential for TNBC using a PLGA (poly-lactic-co-glycolic acid)) nanoparticle delivery system. We formulated it into PLGA nanoparticles to improve bioavailability and enable targeted delivery to TNBC tumors. Various dosages of AXL inhibitor-loaded PLGA nanoparticles were tested on MDA-MB-231 and MDA-MB-436 human TNBC cell lines, and significant inhibition of cell growth and colony formation was observed, with a half-maximal inhibitory concentration (IC50) of 5 μM. The size and morphology of the nanoparticles were characterized using Atomic Force Microscopy (AFM) and Scanning Electron Microscopy (SEM), which revealed nanoparticle sizes ranging from 63-99.9 nm. Western blot analysis showed that the AXL inhibitor-loaded PLGA nanoparticles effectively inhibited AXL protein expression and its downstream signaling pathways, leading to superior anti-proliferative effects compared to free AXL inhibitors. These results suggest that AXL inhibitor-loaded PLGA nanoparticles offer a promising strategy for enhancing the therapeutic efficacy of AXL inhibitors in TNBC. In vivo, efficacy studies are currently underway to evaluate their potential for targeted therapy in both primary and metastatic TNBC models. Citation Format: Fatma Kazdal, Nermin Kahraman, Bulent Ozpolat. Development of novel AXL inhibitor-loaded PLGA nanoparticles for targeted therapy in triple negative breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 1860.
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
7秒前
7秒前
合适乐巧完成签到 ,获得积分10
7秒前
冷傲的怜寒完成签到,获得积分10
29秒前
Everything完成签到,获得积分10
39秒前
水寒风似刀完成签到,获得积分10
50秒前
懦弱的甜瓜完成签到,获得积分10
1分钟前
1分钟前
JamesPei应助科研通管家采纳,获得10
2分钟前
2分钟前
2分钟前
yj发布了新的文献求助10
2分钟前
LONG完成签到 ,获得积分10
2分钟前
默默的以柳完成签到,获得积分10
2分钟前
2分钟前
壮观的菠萝完成签到,获得积分10
2分钟前
CipherSage应助程雀采纳,获得10
3分钟前
光亮豌豆完成签到,获得积分10
3分钟前
3分钟前
微笑的巧蕊完成签到 ,获得积分10
4分钟前
怡然碧空完成签到,获得积分10
4分钟前
4分钟前
zzhui完成签到,获得积分10
5分钟前
隐形大地完成签到,获得积分10
5分钟前
5分钟前
5分钟前
6分钟前
酷波er应助科研通管家采纳,获得10
6分钟前
drfwjuikesv完成签到,获得积分10
6分钟前
6分钟前
留胡子的丹亦完成签到,获得积分10
6分钟前
zyjsunye完成签到 ,获得积分10
6分钟前
6分钟前
6分钟前
朴实的新柔完成签到,获得积分10
6分钟前
7分钟前
7分钟前
哦豁拐咯完成签到 ,获得积分10
7分钟前
7分钟前
无心的月光完成签到,获得积分10
7分钟前
高分求助中
Clinical Epidemiology: The Essentials, 6e 10000
(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
The Graphene Handbook (2019 Edition) 800
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
久松真一著作集〈第5巻〉禅と芸術 500
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6552015
求助须知:如何正确求助?哪些是违规求助? 8338021
关于积分的说明 17864184
捐赠科研通 5666850
什么是DOI,文献DOI怎么找? 2939392
邀请新用户注册赠送积分活动 1915304
关于科研通互助平台的介绍 1783140