%0 Journal Article
%T Transcriptional changes associated with in vivo growth of muscle-invasive bladder cancer cell lines in nude mice
%A Barbara Foster
%A Gissou Azabdaftari
%A Jianmin Wang
%A Joyce Ohm
%A Kevin H Eng
%A Swathi Ramakrishnan
%A Wendy Huss
%J Archive of "American Journal of Clinical and Experimental Urology".
%D 2018
%X Cancer cells set in motion transcriptomic programs allowing for adaptation and growth in immunocompromised mice to form xenografts, a frequently used tool in cancer research. 2D cultures may not be representative of tumors growing in a complex host microenvironment. This can result in different responses to the same agent tested in vitro and in vivo which impedes the process of developing novel therapeutics. Understanding the transition cells undergo from 2D cell culture to a 3D host microenvironment will help in developing and choosing appropriate models for pre-clinical studies. Our study characterized the transcriptome of a three frequently used muscle-invasive bladder cancer cell lines HT1376, T24 and UM-UC-3 grown in culture and xenografts in nude mice. We found that bladder cancer cells undergo few transcriptomic changes when transitioned from 2D cell culture to xenografts in nude mice. UM-UC-3 cells have the least transcriptomic alterations followed by T24 and HT1376 cells. Respective xenografts cluster with their parental cell lines rather than other xenografts or cell lines. We applied established bladder cancer molecular subtypes to our data and found that UM-UC-3, containing the least transcriptomic alterations, most closely resembled the basal-like molecular subtype of bladder cancer. HT1376 and T24 have mixed basal and luminal molecular signatures. Our studies suggest this subset of bladder cancer cell lines and derived xenografts maintain similar transcriptomic profiles in both 2D culture and 3D xenografts and can be used interchangeably in pre-clinical studies
%K Bladder cancer
%K 2D cell culture
%K xenografts
%K molecular subtypes
%K transcriptomics
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055076/