A Transgenic MMTV-Flippase Mouse Line for Molecular Engineering in Mammary Gland and Breast Cancer Mouse Models

被引:0
作者
Fabiana Lüönd
Ruben Bill
Andrea Vettiger
Heide Oller
Pawel Pelczar
Gerhard Christofori
机构
[1] University of Basel,Department of Biomedicine
[2] Biozentrum University of Basel,Focal Area Infection Biology
[3] University of Basel,Center for Transgenic Models
来源
Journal of Mammary Gland Biology and Neoplasia | 2019年 / 24卷
关键词
Breast cancer; Flippase; Lineage tracing; Mammary gland; MMTV promoter; Transgenic mice;
D O I
暂无
中图分类号
学科分类号
摘要
Genetically engineered mouse models have become an indispensable tool for breast cancer research. Combination of multiple site-specific recombination systems such as Cre/loxP and Flippase (Flp)/Frt allows for engineering of sophisticated, multi-layered conditional mouse models. Here, we report the generation and characterization of a novel transgenic mouse line expressing a mouse codon-optimized Flp under the control of the mouse mammary tumor virus (MMTV) promoter. These mice show robust Flp-mediated recombination in luminal mammary gland and breast cancer cells but no Flp activity in non-mammary tissues, with the exception of limited activity in salivary glands. These mice provide a unique tool for studying mammary gland biology and carcinogenesis in mice.
引用
收藏
页码:39 / 45
页数:6
相关论文
共 148 条
  • [1] Borowsky AD(2011)Choosing a mouse model: experimental biology in context--the utility and limitations of mouse models of breast cancer Cold Spring Harb Perspect Biol 3 a009670-123
  • [2] Van Keymeulen A(2015)Reactivation of multipotency by oncogenic PIK3CA induces breast tumour heterogeneity Nature 525 119-118
  • [3] Lee MY(2015)PIK3CA(H1047R) induces multipotency and multi-lineage mammary tumours Nature 525 114-1356
  • [4] Ousset M(2016)Lgr6 labels a rare population of mammary gland progenitor cells that are able to originate luminal mammary tumours Nat Cell Biol 18 1346-606
  • [5] Brohee S(2013)Intravital imaging of cancer stem cell plasticity in mammary tumors Stem Cells 31 602-2288
  • [6] Rorive S(2016)Plasticity between epithelial and mesenchymal states unlinks EMT from metastasis-enhancing stem cell capacity Cell Rep 14 2281-E863
  • [7] Giraddi RR(2016)Polyclonal breast cancer metastases arise from collective dissemination of keratin 14-expressing tumor cell clusters Proc Natl Acad Sci U S A 113 E854-476
  • [8] Koren S(2015)Epithelial-to-mesenchymal transition is not required for lung metastasis but contributes to chemoresistance Nature 527 472-28
  • [9] Reavie L(2004)Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice Dev Cell 6 7-684
  • [10] Couto JP(2016)Site-specific recombinases: molecular machines for the genetic revolution Biochem J 473 673-213