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用于癌症与骨细胞相互作用研究的二维和三维体外共培养

2D and 3D In Vitro Co-culture for Cancer and Bone Cell Interaction Studies.

作者信息

Bishop Ryan T, Delgado-Calle Jesus, Reagan Michaela R, Marino Silvia

机构信息

Department of Tumor Microenvironment and Metastasis, H. Lee Moffitt Cancer Research Center and Institute, Tampa, FL, USA.

Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

出版信息

Methods Mol Biol. 2025;2885:113-141. doi: 10.1007/978-1-0716-4306-8_7.

DOI:10.1007/978-1-0716-4306-8_7
PMID:40448759
Abstract

Co-culture assays are used to study the mutual interaction between cells in vitro. This chapter describes 2D and 3D co-culture systems used to study cell-cell signaling crosstalk between cancer cells and bone marrow adipocytes, osteoblasts, osteoclasts, and osteocytes. The chapter provides a step-by-step guide to the most used cell culture techniques, functional assays, and gene expression.

摘要

共培养分析用于研究体外细胞间的相互作用。本章描述了用于研究癌细胞与骨髓脂肪细胞、成骨细胞、破骨细胞和骨细胞之间细胞间信号串扰的二维和三维共培养系统。本章提供了最常用的细胞培养技术、功能分析和基因表达的分步指南。

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本文引用的文献

1
A NOTCH3-CXCL12-driven myeloma-tumor niche signaling axis promotes chemoresistance in multiple myeloma.一种由NOTCH3-CXCL12驱动的骨髓瘤-肿瘤微环境信号轴促进多发性骨髓瘤的化疗耐药性。
Haematologica. 2024 Aug 1;109(8):2606-2618. doi: 10.3324/haematol.2023.284443.
2
Notch3 signaling between myeloma cells and osteocytes in the tumor niche promotes tumor growth and bone destruction.肿瘤微环境中骨髓瘤细胞和破骨细胞之间的 Notch3 信号转导促进肿瘤生长和骨破坏。
Neoplasia. 2022 Jun;28:100785. doi: 10.1016/j.neo.2022.100785. Epub 2022 Apr 4.
3
Targeting Notch Inhibitors to the Myeloma Bone Marrow Niche Decreases Tumor Growth and Bone Destruction without Gut Toxicity.
靶向骨髓瘤骨髓基质细胞中的 Notch 抑制剂可减少肿瘤生长和骨质破坏而无肠道毒性。
Cancer Res. 2021 Oct 1;81(19):5102-5114. doi: 10.1158/0008-5472.CAN-21-0524. Epub 2021 Aug 4.
4
A pharmacodynamic model of clinical synergy in multiple myeloma.多发性骨髓瘤临床协同作用的药效动力学模型。
EBioMedicine. 2020 Apr;54:102716. doi: 10.1016/j.ebiom.2020.102716. Epub 2020 Apr 5.
5
Aplidin (plitidepsin) is a novel anti-myeloma agent with potent anti-resorptive activity mediated by direct effects on osteoclasts.Aplidin(普利替德生)是一种新型抗骨髓瘤药物,通过对破骨细胞的直接作用介导强大的抗吸收活性。
Oncotarget. 2019 Apr 12;10(28):2709-2721. doi: 10.18632/oncotarget.26831.
6
Genetic deletion of Sost or pharmacological inhibition of sclerostin prevent multiple myeloma-induced bone disease without affecting tumor growth.Sost基因缺失或使用硬化蛋白的药物抑制剂可预防多发性骨髓瘤诱导的骨病,而不影响肿瘤生长。
Leukemia. 2017 Dec;31(12):2686-2694. doi: 10.1038/leu.2017.152. Epub 2017 May 22.
7
An Platform for the Prediction of Clinical Response in Multiple Myeloma.一个用于预测多发性骨髓瘤临床反应的平台。
Cancer Res. 2017 Jun 15;77(12):3336-3351. doi: 10.1158/0008-5472.CAN-17-0502. Epub 2017 Apr 11.
8
Osteocyte isolation and culture methods.骨细胞分离与培养方法。
Bonekey Rep. 2016 Sep 14;5:838. doi: 10.1038/bonekey.2016.65. eCollection 2016.
9
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Microarrays (Basel). 2015 Oct 29;4(4):503-19. doi: 10.3390/microarrays4040503.
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Bone metastasis: the importance of the neighbourhood.骨转移:邻居的重要性。
Nat Rev Cancer. 2016 May 25;16(6):373-86. doi: 10.1038/nrc.2016.44.