2. Academic Validation
  3. Non-cell-autonomous tumor promotion in DICER1 cancer predisposition

Non-cell-autonomous tumor promotion in DICER1 cancer predisposition

  • Dev Cell. 2025 Sep 29:S1534-5807(25)00539-8. doi: 10.1016/j.devcel.2025.09.001.
Randolph K Larsen 4th 1,  Jason A Hanna 2,  Hongjian Jin 3,  Kristin B Reed 2,  Darden W Kimbrough 2,  Kyna Vuong 4,  Jongchan Hwang 2,  Grace E Adkins 1,  Jack D Hopkins 2,  Bradley T Stevens 1,  Myron K Evans 2nd 2,  Casey G Langdon 2,  Catherine J Drummond 2,  Matthew R Garcia 2,  Kristin B Wiggins 5,  Amy R Iverson 6,  David Finkelstein 7,  Patrick A Schreiner 3,  Jason W Rosch 6,  Jerold E Rehg 8,  Kris Ann P Schultz 9,  Mark E Hatley 10
Affiliations

Affiliations

  • 1 St. Jude Graduate School of Biomedical Sciences, Memphis, TN, USA.
  • 2 Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • 3 Center for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • 4 Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA; St. Jude Graduate School of Biomedical Sciences, Memphis, TN, USA.
  • 5 St. Jude Graduate School of Biomedical Sciences, Memphis, TN, USA; Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • 6 Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • 7 Department of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • 8 Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • 9 Cancer and Blood Disorders, Children's Minnesota, Minneapolis, MN, USA; International Pleuropulmonary Blastoma/DICER1 Registry, Children's Minnesota, Minneapolis, MN, USA; International Ovarian and Testicular Stromal Tumor Registry, Children's Minnesota, Minneapolis, MN, USA.
  • 10 Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA; St. Jude Graduate School of Biomedical Sciences, Memphis, TN, USA. Electronic address: mark.hatley@stjude.org.
PMID: 41027427 DOI: 10.1016/j.devcel.2025.09.001
Abstract

DICER1-related tumors are characterized by germline loss-of-function mutations in one DICER1 allele (DICER1+/-) and a somatic "second hit" mutation in the remaining DICER1 allele. Whether the germline DICER1+/- mutation participates in tumorigenesis is unknown. We show that germline heterozygous loss of Dicer1 promotes tumor formation via aberrant neutrophil function in spontaneous and allograft mouse models of rhabdomyosarcoma. Germline heterozygous deletion of Dicer1 decreased tumor latency and increased tumor penetrance, while conditional heterozygous deletion in tumor cells did not, illustrating that non-cell-autonomous contributions were required for tumor promotion. We show that Dicer1+/- murine and human tumors were enriched for neutrophils and that tumor-bearing mice had abundant circulating neutrophil extracellular traps (NETs). Genetically and pharmacologically preventing NET release reduced tumor promotion in Dicer1+/- mice, suggesting NETs promote tumor growth. These findings demonstrate that germline DICER1+/- mutations promote tumor growth and suggest that targeting neutrophils/NET release may reduce Cancer risk in DICER1+/- individuals.

Keywords

DICER; DICER1; NETosis; PADI4; cancer predisposition; microRNA; neutrophil; pediatric cancer; rhabdomyosarcoma; sarcoma.

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