Emerging and Evolving Ovarian Cancer Animal Models.

Cancer growth and metastasis Pub Date : 2015-08-12 eCollection Date: 2015-01-01 DOI:10.4137/CGM.S21221
Alexander S Bobbs, Jennifer M Cole, Karen D Cowden Dahl
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引用次数: 44

Abstract

Ovarian cancer (OC) is the leading cause of death from a gynecological malignancy in the United States. By the time a woman is diagnosed with OC, the tumor has usually metastasized. Mouse models that are used to recapitulate different aspects of human OC have been evolving for nearly 40 years. Xenograft studies in immunocompromised and immunocompetent mice have enhanced our knowledge of metastasis and immune cell involvement in cancer. Patient-derived xenografts (PDXs) can accurately reflect metastasis, response to therapy, and diverse genetics found in patients. Additionally, multiple genetically engineered mouse models have increased our understanding of possible tissues of origin for OC and what role individual mutations play in establishing ovarian tumors. Many of these models are used to test novel therapeutics. As no single model perfectly copies the human disease, we can use a variety of OC animal models in hypothesis testing that will lead to novel treatment options. The goal of this review is to provide an overview of the utility of different mouse models in the study of OC and their suitability for cancer research.

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新兴和发展的卵巢癌动物模型。
卵巢癌(OC)是美国妇科恶性肿瘤死亡的主要原因。当女性被诊断为卵巢癌时,肿瘤通常已经转移。用于概括人类OC不同方面的小鼠模型已经发展了近40年。免疫功能低下和免疫功能正常小鼠的异种移植研究增强了我们对癌症转移和免疫细胞参与的认识。患者来源的异种移植物(PDXs)可以准确反映患者的转移,对治疗的反应和不同的遗传学。此外,多种基因工程小鼠模型增加了我们对卵巢癌可能的起源组织的理解,以及个体突变在建立卵巢肿瘤中所起的作用。其中许多模型被用来测试新的治疗方法。由于没有单一的模型可以完美地复制人类疾病,我们可以在假设检验中使用各种OC动物模型,这将导致新的治疗选择。本综述的目的是概述不同小鼠模型在卵巢癌研究中的应用及其在癌症研究中的适用性。
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