Abstract
Preclinical breast tumor models are an invaluable tool to systematically study tumor progression and treatment response, yet methods to non-invasively monitor the involved molecular and mechanistic properties under physiologically relevant conditions are limited. Here we present an intravital mesoscopic fluorescence molecular tomography (henceforth IFT) approach that is capable of tracking fluorescently labeled tumor cells in a quantitative manner inside the mammary gland of living mice. Our mesoscopic approach is entirely non-invasive and thus permits prolonged observational periods of several months. The relatively high sensitivity and spatial resolution further enable inferring the overall number of oncogene-expressing tumor cells as well as their tumor volume over the entire cycle from early tumor growth to residual disease following the treatment phase. We find that sheer tumor volume, as commonly assessed by other imaging modalities, is not well correlated to tumor cell quantity, hence our IFT approach is a promising new method for studying tumor growth dynamics in a quantitative and longitudinal fashion in-vivo.
Publisher
Cold Spring Harbor Laboratory
Reference65 articles.
1. WHO. Available at: https://www.who.int/cancer/detection/breastcancer/en/.
2. Ductal carcinoma in situ: to treat or not to treat, that is the question;Br. J. Cancer,2019
3. Cancer, R. & U. Identify and target tumour cWells that remain dormant for many years after seemingly effective treatment. (2017). Available at: http://www.cancerresearchuk.org/funding-for-researchers/how-we-deliver-research/grand-challenge-award/dormancy.
4. Models, mechanisms and clinical evidence for cancer dormancy
5. Framework models of tumor dormancy from patient-derived observations