Cell Competition in Carcinogenesis

Author:

Madan Esha1ORCID,Palma António M.1ORCID,Vudatha Vignesh2ORCID,Trevino Jose G.23ORCID,Natarajan Kedar Nath4ORCID,Winn Robert A.3ORCID,Won Kyoung Jae5ORCID,Graham Trevor A.6ORCID,Drapkin Ronny7ORCID,McDonald Stuart A.C.8ORCID,Fisher Paul B.3910ORCID,Gogna Rajan3910ORCID

Affiliation:

1. 1Champalimaud Centre for the Unknown, Lisbon, Portugal.

2. 2Department of Surgery, Virginia Commonwealth University, School of Medicine, Richmond, Virginia.

3. 3VCU Massey Cancer Center, Virginia Commonwealth University, School of Medicine, Richmond, Virginia.

4. 4Technical University of Denmark, Kongens Lyngby, Denmark.

5. 5Department of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, California.

6. 6Evolution and Cancer Laboratory, Centre for Cancer Genomics and Computational Biology, Barts Cancer Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, United Kingdom.

7. 7Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

8. 8Clonal Dynamics in Epithelia Laboratory, Centre for Cancer Genomics and Computational Biology, Barts Cancer Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square. London, United Kingdom.

9. 9Department of Human and Molecular Genetics, Virginia Commonwealth University, School of Medicine, Richmond, Virginia.

10. 10VCU Institute of Molecular Medicine, Virginia Commonwealth University, School of Medicine, Richmond, Virginia.

Abstract

Abstract The majority of human cancers evolve over time through the stepwise accumulation of somatic mutations followed by clonal selection akin to Darwinian evolution. However, the in-depth mechanisms that govern clonal dynamics and selection remain elusive, particularly during the earliest stages of tissue transformation. Cell competition (CC), often referred to as 'survival of the fittest' at the cellular level, results in the elimination of less fit cells by their more fit neighbors supporting optimal organism health and function. Alternatively, CC may allow an uncontrolled expansion of super-fit cancer cells to outcompete their less fit neighbors thereby fueling tumorigenesis. Recent research discussed herein highlights the various non–cell-autonomous principles, including interclonal competition and cancer microenvironment competition supporting the ability of a tumor to progress from the initial stages to tissue colonization. In addition, we extend current insights from CC-mediated clonal interactions and selection in normal tissues to better comprehend those factors that contribute to cancer development.

Funder

National Cancer Institute

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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