• 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

用于胰腺导管腺癌免疫治疗和非免疫治疗药物研发的临床前小鼠模型。

Preclinical mouse models for immunotherapeutic and non-immunotherapeutic drug development for pancreatic ductal adenocarcinoma.

作者信息

He Mengni, Henderson MacKenzie, Muth Stephen, Murphy Adrian, Zheng Lei

机构信息

Department of Cell Biology, Baltimore, MD, USA.

Department of Oncology, Baltimore, MD, USA.

出版信息

Ann Pancreat Cancer. 2020 Jul;3. doi: 10.21037/apc.2020.03.03. Epub 2020 Jul 22.

DOI:10.21037/apc.2020.03.03
PMID:32832900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7440242/
Abstract

Pancreatic ductal adenocarcinoma (PDAC) is in urgent need of better diagnostic and therapeutic methods due to its late diagnosis, limited treatment options and poor prognosis. Finding the right animal models to recapitulate the tumor molecular pathogenesis and tumor microenvironment (TME) complexity is critical for preclinical immunotherapeutic and non-immunotherapeutic treatment developments. In this review, we summarize and evaluate popular preclinical animal models including patient-derived xenograft models, humanized mouse models, genetically engineered mouse models, and syngeneic mouse models. Through comparisons between these models in different research settings, we hope to provide guidance in finding the most relevant preclinical models to suit various research purposes.

摘要

胰腺导管腺癌(PDAC)由于其诊断较晚、治疗选择有限且预后较差,迫切需要更好的诊断和治疗方法。找到合适的动物模型来重现肿瘤分子发病机制和肿瘤微环境(TME)的复杂性对于临床前免疫治疗和非免疫治疗的发展至关重要。在本综述中,我们总结并评估了常用的临床前动物模型,包括患者来源的异种移植模型、人源化小鼠模型、基因工程小鼠模型和同基因小鼠模型。通过在不同研究背景下对这些模型进行比较,我们希望为寻找最适合各种研究目的的相关临床前模型提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/21ae9552fbd1/nihms-1618241-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/342a96bec9b2/nihms-1618241-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/acafce3fae8f/nihms-1618241-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/21ae9552fbd1/nihms-1618241-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/342a96bec9b2/nihms-1618241-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/acafce3fae8f/nihms-1618241-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361e/7440242/21ae9552fbd1/nihms-1618241-f0003.jpg

相似文献

1
Preclinical mouse models for immunotherapeutic and non-immunotherapeutic drug development for pancreatic ductal adenocarcinoma.用于胰腺导管腺癌免疫治疗和非免疫治疗药物研发的临床前小鼠模型。
Ann Pancreat Cancer. 2020 Jul;3. doi: 10.21037/apc.2020.03.03. Epub 2020 Jul 22.
2
Preclinical models of pancreatic ductal adenocarcinoma.胰腺导管腺癌的临床前模型
Chin Clin Oncol. 2017 Jun;6(3):25. doi: 10.21037/cco.2017.06.15.
3
DNA Damage Repair Deficiency in Pancreatic Ductal Adenocarcinoma: Preclinical Models and Clinical Perspectives.胰腺导管腺癌中的DNA损伤修复缺陷:临床前模型与临床前景
Front Cell Dev Biol. 2021 Oct 12;9:749490. doi: 10.3389/fcell.2021.749490. eCollection 2021.
4
Preclinical Models of Pancreatic Ductal Adenocarcinoma and Their Utility in Immunotherapy Studies.胰腺导管腺癌的临床前模型及其在免疫治疗研究中的应用
Cancers (Basel). 2021 Jan 25;13(3):440. doi: 10.3390/cancers13030440.
5
Ultrasound-Guided Orthotopic Implantation of Murine Pancreatic Ductal Adenocarcinoma.超声引导下小鼠胰腺导管腺癌原位植入
J Vis Exp. 2019 Nov 19(153). doi: 10.3791/60497.
6
Challenges and Future Perspectives of Immunotherapy in Pancreatic Cancer.胰腺癌免疫治疗的挑战与未来展望
Cancers (Basel). 2021 Aug 23;13(16):4235. doi: 10.3390/cancers13164235.
7
Desmoplasia and oncogene driven acinar-to-ductal metaplasia are concurrent events during acinar cell-derived pancreatic cancer initiation in young adult mice.促结缔组织增生和癌基因驱动的腺泡到导管化生是在年轻成年小鼠的腺泡细胞衍生的胰腺癌起始过程中同时发生的事件。
PLoS One. 2019 Sep 6;14(9):e0221810. doi: 10.1371/journal.pone.0221810. eCollection 2019.
8
Animal Models of Gastrointestinal and Liver Diseases. The difficulty of animal modeling of pancreatic cancer for preclinical evaluation of therapeutics.胃肠和肝脏疾病的动物模型。用于治疗药物临床前评估的胰腺癌动物建模的困难。
Am J Physiol Gastrointest Liver Physiol. 2015 Sep 1;309(5):G283-91. doi: 10.1152/ajpgi.00169.2015. Epub 2015 Jul 9.
9
Single-cell RNA sequencing reveals compartmental remodeling of tumor-infiltrating immune cells induced by anti-CD47 targeting in pancreatic cancer.单细胞 RNA 测序揭示了抗 CD47 靶向治疗诱导的胰腺癌肿瘤浸润免疫细胞的区室重排。
J Hematol Oncol. 2019 Nov 27;12(1):124. doi: 10.1186/s13045-019-0822-6.
10
Early detection and prevention of pancreatic cancer: use of genetically engineered mouse models and advanced imaging technologies.早期发现和预防胰腺癌:利用基因工程小鼠模型和先进的成像技术。
Curr Med Chem. 2012;19(22):3701-13. doi: 10.2174/092986712801661095.

引用本文的文献

1
PRMT5 Identified as a Viable Target for Combination Therapy in Preclinical Models of Pancreatic Cancer.PRMT5被确定为胰腺癌临床前模型联合治疗的可行靶点。
Biomolecules. 2025 Jun 30;15(7):948. doi: 10.3390/biom15070948.
2
From Genes to Environment: Elucidating Pancreatic Carcinogenesis Through Genetically Engineered and Risk Factor-Integrated Mouse Models.从基因到环境:通过基因工程和风险因素整合小鼠模型阐明胰腺癌发生机制
Cancers (Basel). 2025 May 15;17(10):1676. doi: 10.3390/cancers17101676.
3
A nanoparticle platform for the co-delivery of multiple antigen epitope peptides and STING agonist to lymph nodes for cancer immunotherapy.

本文引用的文献

1
A Yap-Myc-Sox2-p53 Regulatory Network Dictates Metabolic Homeostasis and Differentiation in Kras-Driven Pancreatic Ductal Adenocarcinomas.Yap-Myc-Sox2-p53 调控网络决定了 Kras 驱动的胰腺导管腺癌中的代谢稳态和分化。
Dev Cell. 2019 Oct 7;51(1):113-128.e9. doi: 10.1016/j.devcel.2019.07.022. Epub 2019 Aug 22.
2
Modeling Human Cancer-induced Cachexia.模拟人类癌症恶病质
Cell Rep. 2019 Aug 6;28(6):1612-1622.e4. doi: 10.1016/j.celrep.2019.07.016.
3
Anti-pancreatic tumor efficacy of a Listeria-based, Annexin A2-targeting immunotherapy in combination with anti-PD-1 antibodies.
一种用于将多种抗原表位肽和STING激动剂共同递送至淋巴结以进行癌症免疫治疗的纳米颗粒平台。
Int J Pharm. 2025 Jul 25;680:125757. doi: 10.1016/j.ijpharm.2025.125757. Epub 2025 May 25.
4
EphA2-targeted alpha-particle theranostics for enhancing PDAC treatment.用于增强胰腺癌治疗的 EphA2 靶向α粒子诊疗技术
Theranostics. 2025 Mar 18;15(10):4229-4246. doi: 10.7150/thno.106948. eCollection 2025.
5
Distinct response to IL-1β blockade in liver- and lung-specific metastasis mouse models of pancreatic cancer with heterogeneous tumor microenvironments.在具有异质性肿瘤微环境的胰腺癌肝转移和肺转移小鼠模型中对白细胞介素-1β阻断的不同反应。
Exp Hematol Oncol. 2025 Feb 13;14(1):13. doi: 10.1186/s40164-025-00607-w.
6
Novel Concept of Electrocoagulation and Tumor Cell Implantation: Creation of Minimally Invasive Orthotopic Murine Model of Pancreatic Cancer.电凝与肿瘤细胞植入的新概念:创建胰腺癌微创原位小鼠模型
JSLS. 2024 Oct-Dec;28(4). doi: 10.4293/JSLS.2024.00048. Epub 2025 Jan 17.
7
Advancing pancreatic cancer research and therapeutics: the transformative role of organoid technology.推进胰腺癌研究与治疗:类器官技术的变革性作用。
Exp Mol Med. 2025 Feb;57(1):50-58. doi: 10.1038/s12276-024-01378-w. Epub 2025 Jan 16.
8
Reprogramming tumor-associated macrophages with lipid nanosystems reduces PDAC tumor burden and liver metastasis.用脂质纳米系统重编程肿瘤相关巨噬细胞可减轻胰腺导管腺癌肿瘤负担并减少肝转移。
J Nanobiotechnology. 2024 Dec 24;22(1):795. doi: 10.1186/s12951-024-03010-5.
9
Combating PDAC Drug Resistance: The Role of Ref-1 Inhibitors in Accelerating Progress in Pancreatic Cancer Research.对抗胰腺癌耐药性:Ref-1抑制剂在推动胰腺癌研究进展中的作用
J Cell Signal. 2024;5(4):208-216. doi: 10.33696/signaling.5.126.
10
Overcome the challenge for intratumoral injection of STING agonist for pancreatic cancer by systemic administration.通过全身给药克服胰腺癌瘤内注射STING激动剂的挑战。
J Hematol Oncol. 2024 Aug 7;17(1):62. doi: 10.1186/s13045-024-01576-z.
基于李斯特菌的、靶向膜联蛋白 A2 的免疫疗法联合抗 PD-1 抗体对胰腺癌的抗肿瘤疗效。
J Immunother Cancer. 2019 May 22;7(1):132. doi: 10.1186/s40425-019-0601-5.
4
Discrepancies in the Tumor Microenvironment of Spontaneous and Orthotopic Murine Models of Pancreatic Cancer Uncover a New Immunostimulatory Phenotype for B Cells.自发性和原位胰腺癌细胞小鼠模型的肿瘤微环境差异揭示了 B 细胞的新型免疫刺激表型。
Front Immunol. 2019 Mar 27;10:542. doi: 10.3389/fimmu.2019.00542. eCollection 2019.
5
Development and Biological Analysis of a Novel Orthotopic Peritoneal Dissemination Mouse Model Generated Using a Pancreatic Ductal Adenocarcinoma Cell Line.使用胰腺导管腺癌细胞系构建的新型原位腹膜播散小鼠模型的建立及生物学分析
Pancreas. 2019 Mar;48(3):315-322. doi: 10.1097/MPA.0000000000001253.
6
IDO1 inhibition potentiates vaccine-induced immunity against pancreatic adenocarcinoma.IDO1 抑制增强了针对胰腺腺癌的疫苗诱导免疫。
J Clin Invest. 2019 Apr 1;129(4):1742-1755. doi: 10.1172/JCI124077. Epub 2019 Mar 18.
7
High and low mutational burden tumors versus immunologically hot and cold tumors and response to immune checkpoint inhibitors.高突变负荷肿瘤与低突变负荷肿瘤、免疫原性热肿瘤与冷肿瘤,及其对免疫检查点抑制剂的反应。
J Immunother Cancer. 2018 Dec 27;6(1):157. doi: 10.1186/s40425-018-0479-7.
8
Switchable CAR-T cells mediate remission in metastatic pancreatic ductal adenocarcinoma.可切换的 CAR-T 细胞可介导转移性胰腺导管腺癌缓解。
Gut. 2019 Jun;68(6):1052-1064. doi: 10.1136/gutjnl-2018-316595. Epub 2018 Aug 18.
9
Humanized Mice for the Study of Immuno-Oncology.用于免疫肿瘤学研究的人源化小鼠。
Trends Immunol. 2018 Sep;39(9):748-763. doi: 10.1016/j.it.2018.07.001. Epub 2018 Aug 2.
10
Glypican-1 is enriched in circulating-exosomes in pancreatic cancer and correlates with tumor burden.磷脂酰肌醇蛋白聚糖-1在胰腺癌的循环外泌体中含量丰富,且与肿瘤负荷相关。
Oncotarget. 2018 Apr 10;9(27):19006-19013. doi: 10.18632/oncotarget.24873.