bioRxiv · 10.1101/2020.01.08.898163
Tissue engineered model of hepatic breast cancer micrometastasis shows host-dependent colonization patterns and drug responses
Abstract
Early stages of colonization of distant organs by metastatic cancer cells (micrometastasis) remain almost inaccessible to study due to lack of relevant experimental approaches. Here, we show the first 3D tissue engineered model of hepatic micrometastasis of triple negative breast cancer (TNBC). It reproduces characteristic histopathological features of the disease and reveals that metastatic TNBC cells colonize liver parenchymal and stromal extracellular matrix with different speed and by different strategies. These engineered tumors induce the angiogenic switch when grafted in vivo, confirming their metastatic-specific behaviour. Furthermore, we proved feasibility and biological relevance of our model for drug and nanoparticle testing and found a down-regulatory effect of the liver microenvironment of the sensitivity of TNBC cells to chemotherapeutic drug doxorubicin in free and nanoformulated forms. The convenient and affordable methodology established here can be translated to other types of metastatic tumors for basic cancer biology research and adapted for high-throughput assays.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Guller, A. E., Rozova, V. S., Kuschnerus, I., Khabir, Z., Nadort, A., Garcia-Bennett, A. E., Liang, L., Qian, Y., Goldys, E. M., Zvyagin, A. V.. 2020-01-09. Tissue engineered model of hepatic breast cancer micrometastasis shows host-dependent colonization patterns and drug responses. https://doi.org/10.1101/2020.01.08.898163
Cite the original work for its findings. Save a collection to share your selection of sources.