Germline-specific RNA helicase DDX4 forms cytoplasmic granules in cancer cells and promotes tumor growth

Cell Rep. 2024 Jul 23;43(7):114430. doi: 10.1016/j.celrep.2024.114430. Epub 2024 Jul 3.

Abstract

Cancer cells undergo major epigenetic alterations and transcriptomic changes, including ectopic expression of tissue- and cell-type-specific genes. Here, we show that the germline-specific RNA helicase DDX4 forms germ-granule-like cytoplasmic ribonucleoprotein granules in various human tumors, but not in cultured cancer cells. These cancerous DDX4 complexes contain RNA-binding proteins and splicing regulators, including many known germ granule components. The deletion of DDX4 in cancer cells induces transcriptomic changes and affects the alternative splicing landscape of a number of genes involved in cancer growth and invasiveness, leading to compromised capability of DDX4-null cancer cells to form xenograft tumors in immunocompromised mice. Importantly, the occurrence of DDX4 granules is associated with poor survival in patients with head and neck squamous cell carcinoma and higher histological grade of prostate cancer. Taken together, these results show that the germ-granule-resembling cancerous DDX4 granules control gene expression and promote malignant and invasive properties of cancer cells.

Keywords: CP: Cancer; CP: Molecular biology; DDX4; RNA regulation; RNP granules; cancer; cancer-germline antigens; tumor growth.

MeSH terms

  • Alternative Splicing / genetics
  • Animals
  • Cell Line, Tumor
  • Cell Proliferation
  • Cytoplasmic Granules* / metabolism
  • DEAD-box RNA Helicases* / genetics
  • DEAD-box RNA Helicases* / metabolism
  • Gene Expression Regulation, Neoplastic
  • Germ Cells / metabolism
  • Humans
  • Male
  • Mice
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology

Substances

  • DEAD-box RNA Helicases
  • DDX4 protein, human