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小鼠模型在淋巴瘤研究中的发展及意义

Development and Significance of Mouse Models in Lymphoma Research.

作者信息

Noble Jordan N, Mishra Anjali

机构信息

College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.

Comprehensive Cancer Center, James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, OH, USA.

出版信息

Curr Hematol Malig Rep. 2019 Apr;14(2):119-126. doi: 10.1007/s11899-019-00504-0.

DOI:10.1007/s11899-019-00504-0
PMID:30848424
Abstract

PURPOSE OF REVIEW

Animal models have played an indispensable role in interpreting cancer gene functions, pathogenesis of disease, and in the development of innovative therapeutic approaches targeting aberrant biological pathways in human cancers.

RECENT FINDINGS

These models have guided the therapeutic targeting of cancer-causing mutations and paved the way for assessing anti-cancer drug responses and the preclinical development of immunotherapies. The mammalian models of cancer utilize genetically edited or transplanted mice that develop fairly accurate disease histopathology. The mouse model also allows us to study the effect of tumor microenvironment in the development of lymphoma. The emergence of patient-derived xenografts provides a better opportunity for recapitulating primary lymphoma characteristics and researching personalized drug therapy. In conclusion, the refinement and advancement of available mouse models in lymphoma significantly minimize the therapeutic translational failures in patients.

摘要

综述目的

动物模型在解释癌症基因功能、疾病发病机制以及开发针对人类癌症异常生物学途径的创新治疗方法方面发挥了不可或缺的作用。

最新发现

这些模型指导了针对致癌突变的治疗靶向,为评估抗癌药物反应和免疫疗法的临床前开发铺平了道路。癌症的哺乳动物模型利用基因编辑或移植的小鼠,其能产生相当准确的疾病组织病理学。小鼠模型还使我们能够研究肿瘤微环境在淋巴瘤发展中的作用。患者来源的异种移植的出现为重现原发性淋巴瘤特征和研究个性化药物治疗提供了更好的机会。总之,现有淋巴瘤小鼠模型的完善和进步显著减少了患者治疗转化失败的情况。

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本文引用的文献

1
Cytokine release syndrome: grading, modeling, and new therapy.细胞因子释放综合征:分级、建模和新疗法。
J Hematol Oncol. 2018 Sep 24;11(1):121. doi: 10.1186/s13045-018-0653-x.
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The implication of CRISPR/Cas9 genome editing technology in combating human oncoviruses.CRISPR/Cas9 基因组编辑技术在抗击人类致癌病毒中的意义。
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An EBNA3C-deleted Epstein-Barr virus (EBV) mutant causes B-cell lymphomas with delayed onset in a cord blood-humanized mouse model.
EBNA3C 缺失型 Epstein-Barr 病毒 (EBV) 突变体能在脐血人源化小鼠模型中导致潜伏期较长的 B 细胞淋巴瘤。
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Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells.单核细胞衍生的白细胞介素-1 和白细胞介素-6 对于 CAR T 细胞引起的细胞因子释放综合征和神经毒性是有差异需求的。
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CAR T cell-induced cytokine release syndrome is mediated by macrophages and abated by IL-1 blockade.嵌合抗原受体 T 细胞引起的细胞因子释放综合征是由巨噬细胞介导的,并可通过白细胞介素-1 阻断来减轻。
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Strategic Therapeutic Targeting to Overcome Venetoclax Resistance in Aggressive B-cell Lymphomas.靶向策略克服侵袭性 B 细胞淋巴瘤中 Venetoclax 的耐药性
Clin Cancer Res. 2018 Aug 15;24(16):3967-3980. doi: 10.1158/1078-0432.CCR-17-3004. Epub 2018 Apr 17.
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Ibrutinib plus Venetoclax for the Treatment of Mantle-Cell Lymphoma.伊布替尼联合维奈托克治疗套细胞淋巴瘤。
N Engl J Med. 2018 Mar 29;378(13):1211-1223. doi: 10.1056/NEJMoa1715519.
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Engineering chimeric antigen receptor-T cells for cancer treatment.工程化嵌合抗原受体-T 细胞治疗癌症。
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Augmentation of CD134 (OX40)-dependent NK anti-tumour activity is dependent on antibody cross-linking.OX40(CD134)依赖性 NK 抗肿瘤活性的增强依赖于抗体交联。
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