Neutrophils Alter DNA Repair Landscape to Impact Survival and Shape Distinct Therapeutic Phenotypes of Colorectal Cancer

Gastroenterology. 2021 Jul;161(1):225-238.e15. doi: 10.1053/j.gastro.2021.03.027. Epub 2021 Mar 19.

Abstract

Background & aims: Tumor-infiltrating neutrophils (polymorphonuclear neutrophils [PMNs]) are a prominent feature of colorectal cancer (CRC), where they can promote cytotoxicity or exacerbate disease outcomes. We recently showed that in acute colon injury, PMNs can increase DNA double-strand break (DSB) burden and promote genomic instability via microRNA-dependent inhibition of homologous recombination (HR) repair. In this study, we aimed to establish whether in inflamed colon, neutrophils shape the DSB-repair responses to impact CRC progression and sensitivity/resistance to DNA-repair targeted therapy.

Methods: Human sporadic CRC biopsies, The Cancer Genome Atlas gene expression analyses, tumor xenografts, and murine CRC models, as well as small-molecule inhibition of key DSB-repair factors were leveraged to investigate changes in the DSB-repair landscape and identify unique CRC responses with/without tumor infiltration by PMNs.

Results: We reveal that neutrophils exert a functional dualism in cancer cells, driving temporal modulation of the DNA damage landscape and resolution of DSBs. PMNs were found to promote HR deficiency in low-grade CRC by miR-155-dependent downregulation of RAD51, thus attenuating tumor growth. However, neutrophil-mediated genotoxicity due to accumulation of DSBs led to the induction of non-homologous end-joining (NHEJ), allowing for survival and growth of advanced CRC. Our findings identified a PMN-induced HR-deficient CRC phenotype, featuring low RAD51 and low Ku70 levels, rendering it susceptible to synthetic lethality induced by clinically approved PARP1 inhibitor Olaparib. We further identified a distinct PMN-induced HR-deficient CRC phenotype, featuring high Ku70 and heightened NHEJ, which can be therapeutically targeted by specific inhibition of NHEJ.

Conclusions: Our work delineates 2 mechanism-based translatable therapeutic interventions in sporadic CRC.

Keywords: Colon Cancer; DSB; Ku70; MicroRNA; Rad51.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Coculture Techniques
  • Colitis-Associated Neoplasms / drug therapy
  • Colitis-Associated Neoplasms / genetics
  • Colitis-Associated Neoplasms / immunology*
  • Colitis-Associated Neoplasms / metabolism
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / immunology*
  • Colorectal Neoplasms / metabolism
  • DNA Breaks, Double-Stranded*
  • DNA End-Joining Repair*
  • Databases, Genetic
  • HCT116 Cells
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Humans
  • Ku Autoantigen / genetics
  • Ku Autoantigen / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Neutrophils / immunology*
  • Neutrophils / metabolism
  • Phenotype
  • Poly(ADP-ribose) Polymerase Inhibitors / pharmacology
  • Rad51 Recombinase / genetics
  • Rad51 Recombinase / metabolism
  • Tumor Microenvironment / immunology*
  • Xenograft Model Antitumor Assays

Substances

  • Homeodomain Proteins
  • MIRN155 microRNA, human
  • MicroRNAs
  • Poly(ADP-ribose) Polymerase Inhibitors
  • RAG-1 protein
  • RAD51 protein, human
  • Rad51 Recombinase
  • Xrcc6 protein, human
  • Ku Autoantigen