Cancer Biology and Therapeutics Group, UCD School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland.
BMC Cancer. 2012 May 30;12:209. doi: 10.1186/1471-2407-12-209.
Numerous transgenic models have been generated to study breast cancer. However, despite many advantages, traditional transgenic models for breast cancer are also burdened with difficulties in early detection and longitudinal observation of transgene-induced tumours, which in most cases are randomly located and occur at various time points. Methods such as palpation followed by mechanical measurement of the tumours are of limited value in transgenic models. There is a crucial need for making these previously generated models suitable for modern methods of tumour visualisation and monitoring, e.g. by bioluminescence-based techniques. This approach was successfully used in the current study.
A new mouse strain (MMTV-Luc2 mice) expressing Luc2 luciferase primarily in mammary tissue in females, with low-level background expression in internal organs, was generated and bred to homozygosity. After these mice were intercrossed with MMTV-PyVT mice, all double transgenic females developed mammary tumours by the age of 10 weeks, the localisation and progression of which could be effectively monitored using the luminescence-based in vivo imaging. Luminescence-based readout allowed for early visualisation of the locally overgrown mammary tissue and for longitudinal evaluation of local progression of the tumours. When sampled ex vivo at the age of 10 weeks, all tumours derived from MMTV-Luc2PyVT females displayed robust bioluminescent signal.
We have created a novel transgenic strain for visualisation and longitudinal monitoring of mammary tumour development in transgenic mice as an addition and/or a new and more advanced alternative to manual methods. Generation of this mouse strain is vital for making many of the existing mammary tumour transgenic models applicable for in vivo imaging techniques.
为了研究乳腺癌,已经产生了许多转基因模型。然而,尽管传统的转基因乳腺癌模型有许多优点,但它们也存在一些困难,如难以早期检测和对转基因诱导肿瘤进行纵向观察,因为这些肿瘤通常是随机定位的,并且发生在不同的时间点。传统的方法,如触摸后对肿瘤进行机械测量,在转基因模型中价值有限。因此,迫切需要使这些之前生成的模型适用于肿瘤可视化和监测的现代方法,例如基于生物发光的技术。本研究成功地使用了这种方法。
本研究成功地生成了一种新的小鼠品系(MMTV-Luc2 小鼠),该小鼠在雌性的乳腺组织中主要表达 Luc2 荧光素酶,在内部器官中有低水平的背景表达。然后将该小鼠与 MMTV-PyVT 小鼠杂交,所有雌性双转基因小鼠在 10 周龄时都发展出了乳腺肿瘤,并且可以使用基于发光的体内成像有效地监测肿瘤的定位和进展。基于发光的读数可以早期检测局部过度生长的乳腺组织,并对肿瘤的局部进展进行纵向评估。在 10 周龄时进行离体取样时,所有源自 MMTV-Luc2PyVT 雌性小鼠的肿瘤都显示出强烈的生物发光信号。
我们创建了一种新的转基因品系,用于可视化和纵向监测转基因小鼠的乳腺肿瘤发展,这是对传统手动方法的补充和/或更先进的替代方法。这种小鼠品系的生成对于使许多现有的乳腺肿瘤转基因模型适用于体内成像技术至关重要。