Genetic heterogeneity within collective invasion packs drives leader and follower cell phenotypes

Author:

Zoeller Elizabeth L.1,Pedro Brian1,Konen Jessica1,Dwivedi Bhakti2,Rupji Manali2,Sundararaman Niveda3,Wang Lei4,Horton John R.5,Zhong Chaojie6,Barwick Benjamin G.76,Cheng Xiaodong5,Martinez Elisabeth D.48,Torres Matthew P.3,Kowalski Jeanne29,Marcus Adam I.27,Vertino Paula M.26ORCID

Affiliation:

1. Graduate Program in Cancer Biology, Emory University, Atlanta, GA 30322, USA

2. Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA

3. School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA

4. Hamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX 75390, USA

5. Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

6. Department of Radiation Oncology, Emory University, Atlanta, GA 30322, USA

7. Department of Hematology and Medical Oncology, Emory University, Atlanta, GA 30322, USA

8. Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX 75390, USA

9. Department of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA

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 fourteen 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 shows 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.

Funder

National Institutes of Health

American Cancer Society

Publisher

The Company of Biologists

Subject

Cell Biology

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