Abstract

The immune system plays a major role in the protection against cancer. Identifying and characterizing the pathways mediating this immune surveillance are thus critical for understanding how cancer cells are recognized and eliminated. Aneuploidy is a hallmark of cancer, and we previously found that untransformed cells that had undergone senescence due to highly abnormal karyotypes are eliminated by natural killer (NK) cells in vitro. However, the mechanisms underlying this process remained elusive. Here, using an in vitro NK cell killing system, we show that non‐cell‐autonomous mechanisms in aneuploid cells predominantly mediate their clearance by NK cells. Our data indicate that in untransformed aneuploid cells, NF‐κB signaling upregulation is central to elicit this immune response. Inactivating NF‐κB abolishes NK cell‐mediated clearance of untransformed aneuploid cells. In cancer cell lines, NF‐κB upregulation also correlates with the degree of aneuploidy. However, such upregulation in cancer cells is not sufficient to trigger NK cell‐mediated clearance, suggesting that additional mechanisms might be at play during cancer evolution to counteract NF‐κB‐mediated immunogenicity.

Highlights

  • Aneuploidy is defined as a state in which the chromosome number is not a multiple of the haploid complement (Pfau & Amon, 2012)

  • To address the molecular basis for immune recognition of arrested with complex karyotypes (ArCK) cells, we established a co-culture system to monitor the interactions between natural killer (NK) cells and ArCK cells

  • We previously found that untransformed cells that underwent senescence due to highly abnormal karyotypes are recognized by NK cells in vitro

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Summary

Introduction

Aneuploidy is defined as a state in which the chromosome number is not a multiple of the haploid complement (Pfau & Amon, 2012). Aneuploidies that do survive embryonic development cause significant anatomical and physiological abnormalities (Lindsley et al, 1972; Lorke, 1994; Hassold & Hunt, 2001; Roper & Reeves, 2006). The severe impact of aneuploidy on mammalian physiology is reflected at the cellular level. Trisomic mouse embryonic fibroblasts (MEFs) and aneuploid human cells proliferate more slowly than their euploid counterparts and experience a variety of cellular stresses (Williams et al, 2008; Stingele et al, 2012; Santaguida et al, 2015; Pfau et al, 2016). Replication stress triggers genomic instability and drives the evolution of highly abnormal karyotypes (Sheltzer et al, 2012; Ohashi et al, 2015; Lamm et al, 2016; Passerini et al, 2016; Santaguida et al, 2017)

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