• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[来自胰腺导管腺癌的类器官]

[Organoids from pancreatic ductal adenocarcinoma].

作者信息

Dusetti Nelson, Iovanna Juan

机构信息

Centre de Recherche en Cancérologie de Marseille (CRCM), Inserm U1068, CNRS UMR 7258, Institut Paoli-Calmettes, Aix Marseille Université, Marseille, France.

出版信息

Med Sci (Paris). 2020 Jan;36(1):57-62. doi: 10.1051/medsci/2019259. Epub 2020 Feb 4.

DOI:10.1051/medsci/2019259
PMID:32014099
Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a rapidly evolving and most frequently fatal disease. Despite the enormous progress in understanding the mechanisms related to PDAC pathogenesis, the impact on patient management has not yet been possible. Pancreatic organoids can be generated from small amounts of tissue. One of the most promising applications of organoids is that they can serve as a platform for selecting the right drugs for each patient. This approach has the potential to identify individual therapeutic vulnerabilities by allowing the personalization of treatments. However, these analyzes require several weeks before obtaining enough organoids from the same individual, to carry out the tests with several drugs, and to analyze the results, which limits its use in current clinical practice for the patients with a PDAC, whose it must be remembered that half die within 6 months of diagnosis. To overcome this obstacle, we assessed the ability of transcriptomic molecular signatures to identify patients with a particular sensitivity profile to a given treatment. The approaches based on transcriptomic profiling have the enormous advantage of using very little biological material and thus significantly reducing the time to arrive at the selection of more effective drugs to each patient.

摘要

胰腺导管腺癌(PDAC)是一种迅速发展且最常致命的疾病。尽管在理解与PDAC发病机制相关的机制方面取得了巨大进展,但对患者管理的影响尚未实现。胰腺类器官可以从少量组织中生成。类器官最有前景的应用之一是它们可以作为为每位患者选择合适药物的平台。这种方法有可能通过实现治疗个性化来识别个体治疗弱点。然而,这些分析需要数周时间才能从同一个体获得足够的类器官,以便用几种药物进行测试并分析结果,这限制了其在当前临床实践中对PDAC患者的应用,必须记住,一半的PDAC患者在诊断后6个月内死亡。为了克服这一障碍,我们评估了转录组分子特征识别对特定治疗具有特定敏感性特征的患者的能力。基于转录组分析的方法具有巨大优势,即使用极少的生物材料,从而显著缩短为每位患者选择更有效药物的时间。

相似文献

1
[Organoids from pancreatic ductal adenocarcinoma].[来自胰腺导管腺癌的类器官]
Med Sci (Paris). 2020 Jan;36(1):57-62. doi: 10.1051/medsci/2019259. Epub 2020 Feb 4.
2
Modelling of pancreatic cancer biology: transcriptomic signature for 3D PDX-derived organoids and primary cell line organoid development.胰腺癌生物学建模:基于 3D PDX 衍生类器官和原代细胞系类器官发育的转录组特征。
Sci Rep. 2020 Feb 17;10(1):2778. doi: 10.1038/s41598-020-59368-7.
3
Organoid models for translational pancreatic cancer research.类器官模型在转化胰腺癌研究中的应用。
Curr Opin Genet Dev. 2019 Feb;54:7-11. doi: 10.1016/j.gde.2019.02.003. Epub 2019 Mar 4.
4
Speeding towards individualized treatment for pancreatic cancer by taking an alternative road.另辟蹊径,加速胰腺癌个体化治疗进程。
Cancer Lett. 2017 Dec 1;410:63-67. doi: 10.1016/j.canlet.2017.09.016. Epub 2017 Sep 22.
5
Gene expression profiling of 1200 pancreatic ductal adenocarcinoma reveals novel subtypes.对 1200 例胰腺导管腺癌的基因表达谱分析揭示了新的亚型。
BMC Cancer. 2018 May 29;18(1):603. doi: 10.1186/s12885-018-4546-8.
6
Generation and Culture of Tumor and Metastatic Organoids from Murine Models of Pancreatic Ductal Adenocarcinoma.源自胰腺导管腺癌小鼠模型的肿瘤及转移类器官的生成与培养
Methods Mol Biol. 2019;1882:117-133. doi: 10.1007/978-1-4939-8879-2_10.
7
Immunophenotypes of pancreatic ductal adenocarcinoma: Meta-analysis of transcriptional subtypes.胰腺导管腺癌的免疫表型:转录亚型的荟萃分析。
Int J Cancer. 2019 Aug 15;145(4):1125-1137. doi: 10.1002/ijc.32186. Epub 2019 Mar 18.
8
Generation and Culture of Human Pancreatic Ductal Adenocarcinoma Organoids from Resected Tumor Specimens.从切除的肿瘤标本中生成和培养人胰腺导管腺癌类器官
Methods Mol Biol. 2019;1882:97-115. doi: 10.1007/978-1-4939-8879-2_9.
9
BCAT2-mediated BCAA catabolism is critical for development of pancreatic ductal adenocarcinoma.BCAT2 介导的支链氨基酸分解代谢对于胰腺导管腺癌的发展至关重要。
Nat Cell Biol. 2020 Feb;22(2):167-174. doi: 10.1038/s41556-019-0455-6. Epub 2020 Feb 6.
10
Patient-Derived Organoid Pharmacotyping Guides Precision Medicine for Pancreatic Cancer.患者来源类器官药物代谢分型指导胰腺癌精准医疗。
Clin Cancer Res. 2022 Aug 2;28(15):3176-3178. doi: 10.1158/1078-0432.CCR-22-1083.

引用本文的文献

1
Small Activating RNA Modulation of the G Protein-Coupled Receptor for Cancer Treatment.小分子激活 RNA 调节 G 蛋白偶联受体治疗癌症。
Adv Sci (Weinh). 2022 Sep;9(26):e2200562. doi: 10.1002/advs.202200562. Epub 2022 Jun 16.