Abstract 5236: ARV-110: An androgen receptor PROTAC degrader for prostate cancer

恩扎鲁胺 雄激素受体 前列腺癌 癌症研究 LNCaP公司 雄激素 体内 化学 生物 癌症 内科学 药理学 医学 内分泌学 遗传学 激素
作者
Taavi K. Neklesa,Lawrence B. Snyder,Ryan R. Willard,Nicholas Vitale,Kanak Raina,Jennifer Pizzano,Deborah Gordon,Mark Bookbinder,Jennifer Macaluso,Hanqing Dong,Zheng Liu,Caterina Ferraro,Wang Gan,Jing Wang,Craig M. Crews,John Houston,Andrew P. Crew,I Taylor
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:78 (13_Supplement): 5236-5236 被引量:58
标识
DOI:10.1158/1538-7445.am2018-5236
摘要

Abstract The Androgen Receptor (AR) remains the principal driver of castration-resistant prostate cancer during the transition from a localized to metastatic disease. Most patients initially respond to inhibitors of the AR pathway, but the response is often short-lived. The majority of patients progressing on enzalutamide or abiraterone exhibit genetic alterations in the AR locus, either in the form of amplifications or point mutations in the AR gene. Given these mechanisms of resistance, our goal is to eliminate the AR protein using the PROteolysis TArgeting Chimera (PROTAC) technology. Here we report an orally bioavailable small molecule ARV-110 that leads to ubiquitination and degradation of AR. ARV-110 completely degrades AR in all cell lines tested, with an observed 50% degradation concentration (DC50) < 1 nM. PROTAC-mediated AR degradation suppresses the expression of the AR-target genes PSA and FKBP5, inhibits AR-dependent cell proliferation, and induces potent apoptosis in VCaP cells. ARV-110 degrades clinically relevant mutant AR proteins and retains activity in a high androgen environment. In mouse xenograft studies, greater than 90% AR degradation is observed at a 1 mg/kg PO QD dose. Significant inhibition of tumor growth and AR signaling can be achieved in both an intact and castrate setting. Further, ARV-110 demonstrates in vivo efficacy and reduction of oncogenic Erg protein in a long term, castrate, enzalutamide-resistant VCaP tumor model. DMPK and exploratory toxicology studies show robust oral, dose proportional drug exposure in rodent and non-rodent species. In summary, we report preclinical data on ARV-110, an orally bioavailable androgen receptor PROTAC degrader that demonstrates efficacy in enzalutamide-resistant prostate cancer. Citation Format: Taavi Neklesa, Lawrence B. Snyder, Ryan R. Willard, Nicholas Vitale, Kanak Raina, Jennifer Pizzano, Deborah Gordon, Mark Bookbinder, Jennifer Macaluso, Hanqing Dong, Zheng Liu, Caterina Ferraro, Gan Wang, Jing Wang, Craig M. Crews, John Houston, Andrew P. Crew, Ian Taylor. ARV-110: An androgen receptor PROTAC degrader for prostate cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2018; 2018 Apr 14-18; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2018;78(13 Suppl):Abstract nr 5236.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
亿万斯年应助qian采纳,获得10
2秒前
鱼刺鱼刺卡应助沐11采纳,获得20
3秒前
ding应助多情道之采纳,获得10
6秒前
8秒前
浅帅完成签到,获得积分10
9秒前
希望天下0贩的0应助aaa采纳,获得10
11秒前
12秒前
坤坤发布了新的文献求助10
14秒前
mjhk完成签到,获得积分10
14秒前
好久不见发布了新的文献求助20
15秒前
亿万斯年应助LYF000666采纳,获得20
15秒前
ZD小草完成签到 ,获得积分10
17秒前
17秒前
桐桐应助雨碎寒江采纳,获得10
17秒前
小蘑菇应助浮浮世世采纳,获得10
20秒前
20秒前
20秒前
21秒前
Owen应助sam采纳,获得10
21秒前
YDL发布了新的文献求助10
21秒前
22秒前
Acerie完成签到,获得积分10
23秒前
快乐的鱼发布了新的文献求助10
25秒前
25秒前
你女发布了新的文献求助10
26秒前
木子发布了新的文献求助10
26秒前
量子星尘发布了新的文献求助10
27秒前
pluto应助科研通管家采纳,获得10
28秒前
LaTeXer应助科研通管家采纳,获得150
28秒前
pluto应助科研通管家采纳,获得10
28秒前
llll发布了新的文献求助10
28秒前
28秒前
桐桐应助科研通管家采纳,获得10
28秒前
科研通AI6应助科研通管家采纳,获得10
28秒前
华仔应助科研通管家采纳,获得10
29秒前
桐桐应助科研通管家采纳,获得30
29秒前
pluto应助科研通管家采纳,获得10
29秒前
pluto应助科研通管家采纳,获得10
29秒前
隐形曼青应助科研通管家采纳,获得10
29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
Zeolites: From Fundamentals to Emerging Applications 1500
Architectural Corrosion and Critical Infrastructure 1000
Early Devonian echinoderms from Victoria (Rhombifera, Blastoidea and Ophiocistioidea) 1000
Hidden Generalizations Phonological Opacity in Optimality Theory 1000
Handbook of Social and Emotional Learning, Second Edition 900
2026国自然单细胞多组学大红书申报宝典 800
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 4915038
求助须知:如何正确求助?哪些是违规求助? 4189167
关于积分的说明 13010035
捐赠科研通 3958176
什么是DOI,文献DOI怎么找? 2170103
邀请新用户注册赠送积分活动 1188349
关于科研通互助平台的介绍 1096077