@inproceedings{8365b963e5634ead81226ebe212785ab,
title = "Can engineered micro-scale organotypic models predict patient-specific responses?",
abstract = "Cell-based assays for the prediction of patient-specific cancer response have not been widely adopted. However, it is timely to reevaluate their use, as numerous innovations, including micro-scale organ-on-a-chip models, may improve their predictive power and utility. We demonstrate how different levels of organotypic complexity may be necessary to recapitulate patient response: 1) Co-culture of multiple myeloma cells and stroma from a patient accurately predicts drug chemosensitivity. 2) Invasion of prostate cancer cells into model ECMs allows stratification of patients independent of other biomarkers. 3) Organotypic vessels from patient endothelial cells differentially respond to antiangiogenic therapy in renal cell carcinoma.",
keywords = "Chemosensitivity and resistance, Organ-on-a-chip, Personalized-medicine",
author = "Ingram, {P. N.} and J. Yu and J. Jiminez-Torres and Lee, {M. H.} and Abel, {E. J.} and Basu, {H. S.} and Beebe, {D. J.}",
note = "Funding Information: We acknowledge the contributions of Drs. Chorom Pak, Erwin Berthier, Ashleigh Theberge, Shigeki Miyamoto, and Brian Johnson and funding from the University of Wisconsin Carbone Cancer Center P30 CA014520 and from the NIH R01 CA186134, R01 CA185251, and T32 HL07899.; 20th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2016 ; Conference date: 09-10-2016 Through 13-10-2016",
year = "2016",
language = "English (US)",
series = "20th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2016",
publisher = "Chemical and Biological Microsystems Society",
pages = "122--125",
booktitle = "20th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2016",
}