The Francis Crick Institute
29569246.pdf (657.38 kB)

Expansion of airway basal epithelial cells from primary human non-small cell lung cancer tumors

Download (657.38 kB)
journal contribution
posted on 2020-08-12, 13:32 authored by Robert E Hynds, Assma Ben Aissa, Kate HC Gowers, Thomas BK Watkins, Leticia Bosshard-Carter, Andrew J Rowan, Selvaraju Veeriah, Gareth A Wilson, Sergio A Quezada, Charles Swanton, TRACERx Consortium, Sam M Janes
Pre-clinical non-small cell lung cancer (NSCLC) models are poorly representative of the considerable inter- and intra-tumor heterogeneity of the disease in patients. Primary cell-based in vitro models of NSCLC are therefore desirable for novel therapy development and personalized cancer medicine. Methods have been described to generate rapidly proliferating epithelial cell cultures from multiple human epithelia using 3T3-J2 feeder cell culture in the presence of Y-27632, a RHO-associated protein kinase (ROCK) inhibitor, in what are known as "conditional reprograming conditions" (CRC) or 3T3 + Y. In some cancer studies, variations of this methodology have allowed primary tumor cell expansion across a number of cancer types but other studies have demonstrated the preferential expansion of normal epithelial cells from tumors in such conditions. Here, we report our experience regarding the derivation of primary NSCLC cell cultures from 12 lung adenocarcinoma patients enrolled in the Tracking Cancer Evolution through Therapy (TRACERx) clinical study and discuss these in the context of improving the success rate for in vitro cultivation of cells from NSCLC tumors.