| Literature DB >> 31515279 |
Elizabeth L Zoeller1, Brian Pedro1, Jessica Konen1, Bhakti Dwivedi2, Manali Rupji2, Niveda Sundararaman3, Lei Wang4, John R Horton5, Chaojie Zhong6, Benjamin G Barwick6,7, Xiaodong Cheng5, Elisabeth D Martinez4,8, Matthew P Torres3, Jeanne Kowalski2,9, Adam I Marcus10,7, Paula M Vertino10,6.
Abstract
Collective invasion, the coordinated movement of cohesive packs of cells, has become recognized as a major mode of metastasis for solid tumors. These packs are phenotypically heterogeneous and include specialized cells that lead the invasive pack and others that follow behind. To better understand how these unique cell types cooperate to facilitate collective invasion, we analyzed transcriptomic sequence variation between leader and follower populations isolated from the H1299 non-small cell lung cancer cell line using an image-guided selection technique. We now identify 14 expressed mutations that are selectively enriched in leader or follower cells, suggesting a novel link between genomic and phenotypic heterogeneity within a collectively invading tumor cell population. Functional characterization of two phenotype-specific candidate mutations showed that ARP3 enhances collective invasion by promoting the leader cell phenotype and that wild-type KDM5B suppresses chain-like cooperative behavior. These results demonstrate an important role for distinct genetic variants in establishing leader and follower phenotypes and highlight the necessity of maintaining a capacity for phenotypic plasticity during collective cancer invasion.Entities:
Keywords: Epigenetic; Lung cancer; Metastasis; Mutation; Plasticity; RNA-seq
Year: 2019 PMID: 31515279 PMCID: PMC6803364 DOI: 10.1242/jcs.231514
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285