Targeting NUPR1-dependent stress granules formation to induce synthetic lethality in KrasG12D-driven tumors

EMBO Mol Med. 2024 Mar;16(3):475-505. doi: 10.1038/s44321-024-00032-2. Epub 2024 Feb 15.

Abstract

We find that NUPR1, a stress-associated intrinsically disordered protein, induced droplet formation via liquid-liquid phase separation (LLPS). NUPR1-driven LLPS was crucial for the creation of NUPR1-dependent stress granules (SGs) in pancreatic cancer cells since genetic or pharmacological inhibition by ZZW-115 of NUPR1 activity impeded SGs formation. The KrasG12D mutation induced oncogenic stress, NUPR1 overexpression, and promoted SGs development. Notably, enforced NUPR1 expression induced SGs formation independently of mutated KrasG12D. Mechanistically, KrasG12D expression strengthened sensitivity to NUPR1 inactivation, inducing cell death, activating caspase 3 and releasing LDH. Remarkably, ZZW-115-mediated SG-formation inhibition hampered the development of pancreatic intraepithelial neoplasia (PanINs) in Pdx1-cre;LSL-KrasG12D (KC) mice. ZZW-115-treatment of KC mice triggered caspase 3 activation, DNA fragmentation, and formation of the apoptotic bodies, leading to cell death, specifically in KrasG12D-expressing cells. We further demonstrated that, in developed PanINs, short-term ZZW-115 treatment prevented NUPR1-associated SGs presence. Lastly, a four-week ZZW-115 treatment significantly reduced the number and size of PanINs in KC mice. This study proposes that targeting NUPR1-dependent SGs formation could be a therapeutic approach to induce cell death in KrasG12D-dependent tumors.

Keywords: Kras; NUPR1; Stress Granules; Synthetic Lethality; ZZW-115.

MeSH terms

  • Animals
  • Carcinoma in Situ* / genetics
  • Carcinoma in Situ* / metabolism
  • Carcinoma in Situ* / pathology
  • Carcinoma, Pancreatic Ductal* / genetics
  • Caspase 3 / genetics
  • Caspase 3 / metabolism
  • Mice
  • Pancreatic Neoplasms* / genetics
  • Pancreatic Neoplasms* / pathology
  • Piperazines*
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Stress Granules
  • Synthetic Lethal Mutations
  • Thiazines*

Substances

  • Caspase 3
  • NUPR1 inhibitor ZZW-115
  • Piperazines
  • Proto-Oncogene Proteins p21(ras)
  • Thiazines
  • Nupr1 protein, mouse
  • Hras protein, mouse