Transgenic mouse models of breast cancer. (28th September 2021)

• Record Type: Journal Article
• Authors: Regua, Angelina T.; Arrigo, Austin; Doheny, Daniel; Wong, Grace L.; Lo, Hui-Wen
• Is Part Of: Cancer letters. Volume 516(2021)
• Page Start: 73
• Page End: 83
• Publication Date: 2021-09-28
• Subjects: Breast cancer -- Transgenic mice -- Knockout mice -- Mammary gland -- Tumorigenesis -- Mouse models; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Electronic journals; 616.994
• DOI: 10.1016/j.canlet.2021.05.027
• Languages: English
• ISSNs: 0304-3835

Abstract

Abstract: Transgenic breast cancer mouse models are critical tools for preclinical studies of human breast cancer. Genetic editing of the murine mammary gland allows for modeling of abnormal genetic events frequently found in human breast cancers. Genetically engineered mouse models (GEMMs) of breast cancer employ tissue-specific genetic manipulation for tumorigenic induction within the mammary tissue. Under the transcriptional control of mammary-specific promoters, transgenic mouse models can simulate spontaneous mammary tumorigenesis by expressing one or more putative oncogenes, such as MYC, HRAS, and PIK3CA . Alternatively, the Cre-Lox system allows for tissue-specific deletion of tumor suppressors, such as p53, Rb1, and Brca1, or specific knock-in of putative oncogenes. Thus, GEMMs can be designed to implement one or more genetic events to induce mammary tumorigenesis. Features of GEMMs, such as age of transgene expression, breeding quality, tumor latency, histopathological characteristics, and propensity for local and distant metastasis, are variable and strain-dependent. This review aims to summarize currently available transgenic breast cancer mouse models that undergo spontaneous mammary tumorigenesis upon genetic manipulation, their varying characteristics, and their individual genetic manipulations that model aberrant signaling events observed in human breast cancers. Highlights: Transgenic mouse models can model known subtypes of human breast cancer. Multi-transgenic mouse models can be generated to model human breast cancer cases. Mammary-specific gene editing can induce spontaneous murine mammary tumorigenesis. Background strains of transgenic mice can impact mammary tumor characteristics.