已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

MP11-05 TUMOR HETEROGENEITY AND DRUG SENSITIVITY MODELLED IN PRIMARY PROSTATE CANCER ORGANOIDS

类有机物 前列腺癌 医学 离体 癌症 癌症研究 前列腺 药品 病理 肿瘤科 体内 内科学 生物 药理学 遗传学
作者
Juening Kang,Sofia Karkampouna,Katja Ovchinnikova,Panagiotis Chouvardas,Marianna Kruithof-de Julio,George N. Thalmann
出处
期刊:The Journal of Urology [Ovid Technologies (Wolters Kluwer)]
卷期号:209 (Supplement 4)
标识
DOI:10.1097/ju.0000000000003226.05
摘要

You have accessJournal of UrologyCME1 Apr 2023MP11-05 TUMOR HETEROGENEITY AND DRUG SENSITIVITY MODELLED IN PRIMARY PROSTATE CANCER ORGANOIDS Juening Kang, Sofia Karkampouna, Katja Ovchinnikova, Panagiotis Chouvardas, Marianna Kruithof-de Julio, and George Thalmann Juening KangJuening Kang More articles by this author , Sofia KarkampounaSofia Karkampouna More articles by this author , Katja OvchinnikovaKatja Ovchinnikova More articles by this author , Panagiotis ChouvardasPanagiotis Chouvardas More articles by this author , Marianna Kruithof-de JulioMarianna Kruithof-de Julio More articles by this author , and George ThalmannGeorge Thalmann More articles by this author View All Author Informationhttps://doi.org/10.1097/JU.0000000000003226.05AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract INTRODUCTION AND OBJECTIVE: Prostate cancer (PCa) is a highly heterogeneous and multifocal disease. We hypothesize that heterogeneous lesions, in terms of genomic aberrations and tumour staging, may be linked to different functional properties such as drug response. Here we investigate which histopathological and molecular properties are associated with ability to maintain PCa cells as organoid cultures and specific ex vivo drug responses. METHODS: To simultaneously assess the histopathology, genetic profile and organoid drug sensitivity, we employed mirror biopsies for FFPE and cell preparations. Four cores of prostate tissue from radical prostatectomies (N=13) were used for generating patient-derived organoids (PDOs). Targeted genomic sequencing was performed on PDOs and their parental FFPE tissues. Drug response was evaluated by ATP-based viability assay after treatment with standard-of-care (AR inhibitors), and approved compounds for other malignancies (DNA synthesis, receptor tyrosine kinase (RTK) and mTOR inhibitors). RNA sequencing was performed on the parental cores. RESULTS: Histologically heterogeneous cores with different Gleason Score (GS range 6 to 9) per prostate were found in 76% of cases (N=10/13). PDO formation efficiency was high; 78% of tumor-containing cores (N=22/28) and 66% of benigncores (N=16/24). PCa somatic mutations were found in 19/32 cores, from which the 11 cores had common mutations with their matching PDOs. The transcriptomic signature of each case was overall preserved among different cores. Drug responses in PDOs revealed intra-patient heterogeneity with only 2 patient cases (N=2/13) having positive correlation within the different cores (Pearson’s R=0.58, 0.72). Instead, RTK inhibitors, Crizotinib and Ponatinib,showed high efficacy in the majority of cases (p<0.01 over vehicle, N=29/32 and N=30/32, respectively). Differential expression analysis on the parental tissues indicated that high JAK/STAT expression correlates with high PDO sensitivity to Ponatinib, thus potentially discriminating responders versus non responders. CONCLUSIONS: The majority of primary PCa cases showed genetic and histopathological multifocality, representing a highly heterogeneous cohort. PDOs recapitulated the genetic signature of the parental tissues. Drug responses of PDOs revealed high inter- and intra-patient heterogeneity. Associations among specific mutations, transcriptomic profile and PDO responses are being further explored using machine learning algorithms towards drug response prediction. Source of Funding: Swiss National Foundation, Personalized Health and Related Technologies, The Swiss 3R Competence Centre © 2023 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 209Issue Supplement 4April 2023Page: e125 Advertisement Copyright & Permissions© 2023 by American Urological Association Education and Research, Inc.MetricsAuthor Information Juening Kang More articles by this author Sofia Karkampouna More articles by this author Katja Ovchinnikova More articles by this author Panagiotis Chouvardas More articles by this author Marianna Kruithof-de Julio More articles by this author George Thalmann More articles by this author Expand All Advertisement PDF downloadLoading ...

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
111111完成签到 ,获得积分10
刚刚
缓慢天菱完成签到,获得积分10
2秒前
田様应助原野小年采纳,获得10
2秒前
懵懂的半蕾完成签到 ,获得积分10
4秒前
MIO完成签到,获得积分10
6秒前
8秒前
1111chen完成签到 ,获得积分20
11秒前
阿鑫完成签到 ,获得积分10
13秒前
li完成签到 ,获得积分10
14秒前
14秒前
铁臂阿童木完成签到,获得积分10
15秒前
紫色翡翠完成签到,获得积分10
15秒前
寂寞的寄文完成签到 ,获得积分10
15秒前
huanhuan完成签到 ,获得积分10
19秒前
原野小年发布了新的文献求助10
19秒前
21秒前
木头人呐完成签到 ,获得积分10
22秒前
阳光傲菡完成签到 ,获得积分10
25秒前
26秒前
yy完成签到 ,获得积分10
27秒前
WHY完成签到 ,获得积分10
27秒前
王子发布了新的文献求助10
28秒前
隔壁小黄完成签到 ,获得积分10
30秒前
RADIUM三餐都要吃肉完成签到 ,获得积分10
36秒前
37秒前
无私的含海完成签到,获得积分10
37秒前
糟糕的冬莲完成签到 ,获得积分10
38秒前
39秒前
小点点完成签到,获得积分10
40秒前
40秒前
42秒前
44秒前
47秒前
Hasee完成签到 ,获得积分10
47秒前
47秒前
yourbigdaddy完成签到 ,获得积分10
48秒前
49秒前
耳东发布了新的文献求助10
52秒前
向阳葵完成签到 ,获得积分10
52秒前
滾滾发布了新的文献求助10
53秒前
高分求助中
Evolution 10000
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Foreign Policy of the French Second Empire: A Bibliography 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
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 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3146637
求助须知:如何正确求助?哪些是违规求助? 2797945
关于积分的说明 7826268
捐赠科研通 2454478
什么是DOI,文献DOI怎么找? 1306280
科研通“疑难数据库(出版商)”最低求助积分说明 627692
版权声明 601522