USP19 exacerbates lipogenesis and colorectal carcinogenesis by stabilizing ME1

Cell Rep. 2021 Dec 28;37(13):110174. doi: 10.1016/j.celrep.2021.110174.

Abstract

Lipogenesis plays a critical role in colorectal carcinogenesis, but precisely how remains unclear. Here, we show that ERK2 phosphorylates ME1 at T103, thereby inhibiting its polyubiquitination and proteasomal degradation and enhancing its interaction with USP19. USP19 antagonizes RNF1-mediated ME1 degradation by deubiquitination, which in turn promotes lipid metabolism and NADPH production and suppresses ROS. Meanwhile, ROS dramatically increases PD-L1 mRNA levels through accelerating expression of the transcription factor NRF2. Increased lipid metabolism is correlated with ERK2 activity and colorectal carcinogenesis in human patients. Therefore, the combination of ERK2 inhibitor and anti-PD-L1 antibody significantly inhibits spontaneous and chemically induced colorectal carcinogenesis. Collectively, the USP19-ME1 axis plays a vital role in colorectal carcinogenesis and may also provide a potential therapeutic target.

Keywords: ME1; PD-L1; USP19; deubiquitination; lipogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Aminopyridines / pharmacology
  • Animals
  • B7-H1 Antigen / antagonists & inhibitors*
  • Carcinogenesis
  • Case-Control Studies
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Endopeptidases / genetics
  • Endopeptidases / metabolism*
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / pharmacology
  • Lipogenesis*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Mitogen-Activated Protein Kinase 1 / antagonists & inhibitors*
  • Phosphorylation
  • Pyrroles / pharmacology
  • Reactive Oxygen Species / metabolism
  • Ubiquitination*
  • Vesicular Transport Proteins / chemistry*
  • Vesicular Transport Proteins / genetics
  • Vesicular Transport Proteins / metabolism

Substances

  • Aminopyridines
  • B7-H1 Antigen
  • CD274 protein, human
  • Immune Checkpoint Inhibitors
  • NPC2 protein, human
  • Pyrroles
  • Reactive Oxygen Species
  • Vesicular Transport Proteins
  • ulixertinib
  • MAPK1 protein, human
  • Mitogen-Activated Protein Kinase 1
  • Endopeptidases
  • USP19 protein, human