Jerry Usary, David Brian Darr, Adam D. Pfefferle, Charles M. Perou
{"title":"Overview of Genetically Engineered Mouse Models of Distinct Breast Cancer Subtypes","authors":"Jerry Usary, David Brian Darr, Adam D. Pfefferle, Charles M. Perou","doi":"10.1002/0471141755.ph1438s72","DOIUrl":null,"url":null,"abstract":"<p>Advances in the screening of new therapeutic options have significantly reduced the breast cancer death rate over the last decade. Despite these advances, breast cancer remains the second leading cause of cancer death among women. This is due in part to the complexity of the disease, which is characterized by multiple subtypes that are driven by different genetic mechanisms and that likely arise from different cell types of origin. Because these differences often drive treatment options and outcomes, it is important to select relevant preclinical model systems to study new therapeutic interventions and tumor biology. Described in this unit are the characteristics and applications of validated genetically engineered mouse models (GEMMs) of basal-like, luminal, and claudin-low human subtypes of breast cancer. These different subtypes have different clinical outcomes and require different treatment strategies. These GEMMs can be considered faithful surrogates of their human disease counterparts. They represent alternative preclinical tumor models to cell line and patient-derived xenografts for preclinical drug discovery and tumor biology studies. © 2016 by John Wiley & Sons, Inc.</p>","PeriodicalId":10871,"journal":{"name":"Current Protocols in Pharmacology","volume":"72 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/0471141755.ph1438s72","citationCount":"26","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/0471141755.ph1438s72","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 26
Abstract
Advances in the screening of new therapeutic options have significantly reduced the breast cancer death rate over the last decade. Despite these advances, breast cancer remains the second leading cause of cancer death among women. This is due in part to the complexity of the disease, which is characterized by multiple subtypes that are driven by different genetic mechanisms and that likely arise from different cell types of origin. Because these differences often drive treatment options and outcomes, it is important to select relevant preclinical model systems to study new therapeutic interventions and tumor biology. Described in this unit are the characteristics and applications of validated genetically engineered mouse models (GEMMs) of basal-like, luminal, and claudin-low human subtypes of breast cancer. These different subtypes have different clinical outcomes and require different treatment strategies. These GEMMs can be considered faithful surrogates of their human disease counterparts. They represent alternative preclinical tumor models to cell line and patient-derived xenografts for preclinical drug discovery and tumor biology studies. © 2016 by John Wiley & Sons, Inc.
不同乳腺癌亚型的基因工程小鼠模型综述
在过去十年中,在筛选新的治疗方案方面取得的进展大大降低了乳腺癌死亡率。尽管取得了这些进展,但乳腺癌仍然是妇女癌症死亡的第二大原因。这部分是由于该疾病的复杂性,其特点是由不同的遗传机制驱动的多种亚型,可能来自不同的细胞类型起源。由于这些差异通常会影响治疗方案和结果,因此选择相关的临床前模型系统来研究新的治疗干预和肿瘤生物学是很重要的。本单元描述了经过验证的基因工程小鼠模型(GEMMs)的特点和应用,这些模型包括基底样、腔型和低claudin人类乳腺癌亚型。这些不同的亚型有不同的临床结果,需要不同的治疗策略。这些gem可以被认为是人类疾病对应体的忠实替代品。它们为临床前药物发现和肿瘤生物学研究提供了细胞系和患者来源的异种移植物的替代临床前肿瘤模型。©2016 by John Wiley &儿子,Inc。
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