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重症联合免疫缺陷-人骨髓瘤模型

The SCID-hu myeloma model.

作者信息

Epstein Joshua, Yaccoby Shmuel

机构信息

Myeloma Institute for Research and Therapy, University of Arkansas for Medical Science, Little Rock, AK, USA.

出版信息

Methods Mol Med. 2005;113:183-90. doi: 10.1385/1-59259-916-8:183.

DOI:10.1385/1-59259-916-8:183
PMID:15968103
Abstract

The severe combined immune deficient human (SCID-hu) myeloma model is the only available model in which primary myeloma cells grow in vivo in a human bone marrow micro environment. A SCID mouse receives an implanted human fetal bone into which myeloma cells are directly injected. Through interaction with the human bone marrow microenvironment, the myeloma cells induce typical myeloma manifestations in the SCID host, such as the appearance of M protein in the serum, and changes in the implanted human bone, which often result in osteolysis of the human bone. The model provides the only platform for in vivo investigation of the biology and therapy of primary human myeloma in a human microenvironment. This chapter describes in detail all the steps necessary to establish this model and evaluate its success.

摘要

严重联合免疫缺陷人类(SCID-hu)骨髓瘤模型是唯一可用的模型,在该模型中,原发性骨髓瘤细胞可在人类骨髓微环境中于体内生长。一只SCID小鼠接受植入的人类胎儿骨,然后将骨髓瘤细胞直接注射到其中。通过与人类骨髓微环境相互作用,骨髓瘤细胞在SCID宿主中诱发典型的骨髓瘤表现,例如血清中出现M蛋白,以及植入的人类骨发生变化,这常常导致人类骨的骨质溶解。该模型为在人类微环境中对原发性人类骨髓瘤的生物学特性和治疗方法进行体内研究提供了唯一的平台。本章详细描述了建立该模型并评估其是否成功所需的所有步骤。

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1
The SCID-hu myeloma model.重症联合免疫缺陷-人骨髓瘤模型
Methods Mol Med. 2005;113:183-90. doi: 10.1385/1-59259-916-8:183.
2
Combination therapy with interleukin-6 receptor superantagonist Sant7 and dexamethasone induces antitumor effects in a novel SCID-hu In vivo model of human multiple myeloma.白细胞介素-6受体超级拮抗剂Sant7与地塞米松联合治疗在一种新型人多发性骨髓瘤SCID-hu体内模型中诱导抗肿瘤作用。
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The development of a model for the homing of multiple myeloma cells to human bone marrow.多发性骨髓瘤细胞归巢至人骨髓的模型构建
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引用本文的文献

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Laboratory Mice - A Driving Force in Immunopathology and Immunotherapy Studies of Human Multiple Myeloma.实验室小鼠——人类多发性骨髓瘤免疫病理学和免疫治疗研究的推动力量。
Front Immunol. 2021 Jun 2;12:667054. doi: 10.3389/fimmu.2021.667054. eCollection 2021.
2
Bone-targeted agents in multiple myeloma.多发性骨髓瘤中的骨靶向药物。
Hematol Rep. 2018 Mar 29;10(1):7401. doi: 10.4081/hr.2018.7401. eCollection 2018 Mar 2.
3
Whole Genome Sequence of Multiple Myeloma-Prone C57BL/KaLwRij Mouse Strain Suggests the Origin of Disease Involves Multiple Cell Types.
易患多发性骨髓瘤的C57BL/KaLwRij小鼠品系的全基因组序列表明,疾病起源涉及多种细胞类型。
PLoS One. 2015 May 28;10(5):e0127828. doi: 10.1371/journal.pone.0127828. eCollection 2015.
4
NOD/SCID-GAMMA mice are an ideal strain to assess the efficacy of therapeutic agents used in the treatment of myeloma bone disease.NOD/SCID-γ小鼠是评估用于治疗骨髓瘤骨病的治疗药物疗效的理想品系。
PLoS One. 2015 Mar 13;10(3):e0119546. doi: 10.1371/journal.pone.0119546. eCollection 2015.
5
β-catenin is dynamically stored and cleared in multiple myeloma by the proteasome-aggresome-autophagosome-lysosome pathway.β-连环蛋白在多发性骨髓瘤中通过蛋白酶体-聚集体自噬体-溶酶体途径被动态储存和清除。
Leukemia. 2012 May;26(5):1116-9. doi: 10.1038/leu.2011.303. Epub 2011 Nov 4.
6
Tracking human multiple myeloma xenografts in NOD-Rag-1/IL-2 receptor gamma chain-null mice with the novel biomarker AKAP-4.用新型生物标志物 AKAP-4 追踪 NOD-Rag-1/IL-2 受体 γ 链缺陷小鼠中的人多发性骨髓瘤异种移植物。
BMC Cancer. 2011 Sep 16;11:394. doi: 10.1186/1471-2407-11-394.
7
Pharmaceutical inhibition of glycogen synthetase kinase-3β reduces multiple myeloma-induced bone disease in a novel murine plasmacytoma xenograft model.药物抑制糖原合酶激酶-3β可减少新型骨髓瘤异种移植模型中多发性骨髓瘤引起的骨病。
Blood. 2011 Feb 3;117(5):1641-51. doi: 10.1182/blood-2010-09-308171. Epub 2010 Dec 1.
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Targeting the bone microenvironment in multiple myeloma.靶向多发性骨髓瘤的骨微环境。
J Bone Miner Metab. 2010 May;28(3):244-50. doi: 10.1007/s00774-009-0154-7. Epub 2010 Feb 4.
9
Combinatorial efficacy of anti-CS1 monoclonal antibody elotuzumab (HuLuc63) and bortezomib against multiple myeloma.抗 CS1 单克隆抗体依鲁替尼(HuLuc63)联合硼替佐米治疗多发性骨髓瘤的组合疗效。
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