| Literature DB >> 34529939 |
Nathaniel R Campbell1, Anjali Rao2, Miranda V Hunter3, Magdalena K Sznurkowska4, Luzia Briker5, Maomao Zhang3, Maayan Baron2, Silja Heilmann6, Maxime Deforet6, Colin Kenny7, Lorenza P Ferretti8, Ting-Hsiang Huang3, Sarah Perlee3, Manik Garg9, Jérémie Nsengimana10, Massimo Saini4, Emily Montal3, Mohita Tagore3, Julia Newton-Bishop10, Mark R Middleton11, Pippa Corrie12, David J Adams13, Roy Rabbie14, Nicola Aceto4, Mitchell P Levesque5, Robert A Cornell7, Itai Yanai2, Joao B Xavier15, Richard M White16.
Abstract
Melanomas can have multiple coexisting cell states, including proliferative (PRO) versus invasive (INV) subpopulations that represent a "go or grow" trade-off; however, how these populations interact is poorly understood. Using a combination of zebrafish modeling and analysis of patient samples, we show that INV and PRO cells form spatially structured heterotypic clusters and cooperate in the seeding of metastasis, maintaining cell state heterogeneity. INV cells adhere tightly to each other and form clusters with a rim of PRO cells. Intravital imaging demonstrated cooperation in which INV cells facilitate dissemination of less metastatic PRO cells. We identified the TFAP2 neural crest transcription factor as a master regulator of clustering and PRO/INV states. Isolation of clusters from patients with metastatic melanoma revealed a subset with heterotypic PRO-INV clusters. Our data suggest a framework for the co-existence of these two divergent cell populations, in which heterotypic clusters promote metastasis via cell-cell cooperation.Entities:
Keywords: TFAP2; circulating tumor cell cluster; cluster; cooperation; melanoma; metastasis; zebrafish
Mesh:
Year: 2021 PMID: 34529939 PMCID: PMC8551056 DOI: 10.1016/j.devcel.2021.08.018
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270