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动物模型在多发性骨髓瘤中的应用。

The use of animal models in multiple myeloma.

作者信息

Libouban H

机构信息

GEROM groupe études remodelage osseux et biomatériaux-LHEA, IRIS-IBS institut de biologie en santé, LUNAM université, CHU d'Angers, 49933 Angers cedex, France.

出版信息

Morphologie. 2015 Jun;99(325):63-72. doi: 10.1016/j.morpho.2015.01.003. Epub 2015 Apr 17.

DOI:10.1016/j.morpho.2015.01.003
PMID:25898798
Abstract

In myeloma, the understanding of the tissular, cellular and molecular mechanisms of the interactions between tumor plasma cells and bone cells have progressed from in vitro and in vivo studies. However none of the known animal models of myeloma reproduce exactly the human form of the disease. There are currently three types of animal models: (1) injection of pristane oil in BALB/c mice leads to intraperitoneal plasmacytomas but without bone marrow colonization and osteolysis; (2) injection of malignant plasma cell lines in immunodeficient mice SCID or NOD/SCID; the use of the SCID-hu or SCID-rab model allows the use of fresh plasma cells obtained from MM patients; (3) injection of allogeneic malignant plasma cells (5T2MM, 5T33) in the C57BL/KalwRij mouse induces bone marrow proliferation and osteolytic lesions. These cells did not grow in vitro and can be propagated by injection of plasma cells isolated from bone marrow of a mouse at end stage of the disease into young recipient mice. The 5TGM1 is a subclone of 5T33MM cells and can grow in vitro. Among the different models, the 5TMM models and SCID-hu/SCID-rab models were extensively used to test pathophysiological hypotheses and to assess anti-osteoclastic, anti-osteoblastic or anti-tumor therapies in myeloma. In the present review, we report the different types of animal models of MM and describe their interests and limitations.

摘要

在骨髓瘤中,通过体外和体内研究,对肿瘤浆细胞与骨细胞相互作用的组织、细胞和分子机制的理解取得了进展。然而,目前已知的骨髓瘤动物模型均不能完全重现人类疾病形式。目前有三种类型的动物模型:(1)向BALB/c小鼠注射 pristane 油可导致腹腔浆细胞瘤,但不会出现骨髓定植和骨溶解;(2)向免疫缺陷小鼠SCID或NOD/SCID注射恶性浆细胞系;使用SCID-hu或SCID-rab模型可使用从MM患者获得的新鲜浆细胞;(3)向C57BL/KalwRij小鼠注射同种异体恶性浆细胞(5T2MM、5T33)可诱导骨髓增殖和溶骨性病变。这些细胞在体外不能生长,可通过将疾病终末期小鼠骨髓中分离的浆细胞注射到年轻受体小鼠中来进行传代培养。5TGM1是5T33MM细胞的一个亚克隆,可在体外生长。在不同模型中,5TMM模型和SCID-hu/SCID-rab模型被广泛用于检验病理生理假说,并评估骨髓瘤的抗破骨细胞、抗成骨细胞或抗肿瘤治疗。在本综述中,我们报告了MM的不同类型动物模型,并描述了它们的优点和局限性。

相似文献

1
The use of animal models in multiple myeloma.动物模型在多发性骨髓瘤中的应用。
Morphologie. 2015 Jun;99(325):63-72. doi: 10.1016/j.morpho.2015.01.003. Epub 2015 Apr 17.
2
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.
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Inhibition of p38alpha mitogen-activated protein kinase prevents the development of osteolytic bone disease, reduces tumor burden, and increases survival in murine models of multiple myeloma.抑制p38α丝裂原活化蛋白激酶可预防溶骨性骨病的发展,减轻肿瘤负担,并提高多发性骨髓瘤小鼠模型的生存率。
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Nonirradiated NOD/SCID-human chimeric animal model for primary human multiple myeloma: a potential in vivo culture system.用于原发性人类多发性骨髓瘤的非照射NOD/SCID-人类嵌合动物模型:一种潜在的体内培养系统。
Am J Pathol. 2004 Feb;164(2):747-56. doi: 10.1016/S0002-9440(10)63162-8.
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Inhibiting Dickkopf-1 (Dkk1) removes suppression of bone formation and prevents the development of osteolytic bone disease in multiple myeloma.抑制Dickkopf-1(Dkk1)可消除对骨形成的抑制,并预防多发性骨髓瘤中溶骨性骨病的发展。
J Bone Miner Res. 2009 Mar;24(3):425-36. doi: 10.1359/jbmr.081104.
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Mouse plasmacytoma: an experimental model of human multiple myeloma.小鼠浆细胞瘤:人类多发性骨髓瘤的实验模型。
Haematologica. 2001 Mar;86(3):227-36.
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A review of current murine models of multiple myeloma used to assess the efficacy of therapeutic agents on tumour growth and bone disease.对目前用于评估治疗药物对肿瘤生长和骨病疗效的多发性骨髓瘤小鼠模型的综述。
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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.
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In vivo models of multiple myeloma (MM).多发性骨髓瘤(MM)的体内模型。
Biochem Pharmacol. 2014 Jun 1;89(3):313-20. doi: 10.1016/j.bcp.2014.03.013. Epub 2014 Apr 1.
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Selection of a highly aggressive myeloma cell line by an altered bone microenvironment in the C57BL/KaLwRij mouse.C57BL/KaLwRij小鼠中改变的骨微环境对高侵袭性骨髓瘤细胞系的选择
Biochem Biophys Res Commun. 2004 Apr 9;316(3):859-66. doi: 10.1016/j.bbrc.2004.02.131.

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