|Publication Type||Journal Article|
|Year of Publication||2020|
|Authors||Kinker, GS, Greenwald, AC, Tal, R, Orlova, Z, Cuoco, MS, McFarland, JM, Warren, A, Rodman, C, Roth, JA, Bender, SA, Kumar, B, Rocco, JW, Fernandes, PACM, Mader, CC, Keren-Shaul, H, Plotnikov, A, Barr, H, Tsherniak, A, Rozenblatt-Rosen, O, Krizhanovsky, V, Puram, SV, Regev, A, Tirosh, I|
|Date Published||2020 11|
Cultured cell lines are the workhorse of cancer research, but the extent to which they recapitulate the heterogeneity observed among malignant cells in tumors is unclear. Here we used multiplexed single-cell RNA-seq to profile 198 cancer cell lines from 22 cancer types. We identified 12 expression programs that are recurrently heterogeneous within multiple cancer cell lines. These programs are associated with diverse biological processes, including cell cycle, senescence, stress and interferon responses, epithelial-mesenchymal transition and protein metabolism. Most of these programs recapitulate those recently identified as heterogeneous within human tumors. We prioritized specific cell lines as models of cellular heterogeneity and used them to study subpopulations of senescence-related cells, demonstrating their dynamics, regulation and unique drug sensitivities, which were predictive of clinical response. Our work describes the landscape of heterogeneity within diverse cancer cell lines and identifies recurrent patterns of heterogeneity that are shared between tumors and specific cell lines.
|Alternate Journal||Nat Genet|
|Grant List||K08 CA237732 / CA / NCI NIH HHS / United States |
/ HHMI / Howard Hughes Medical Institute / United States