DOI: 10.1002/iub.2792 ISSN: 1521-6543

Amino acid deprivation induces TXNIP expression by NRF2 downregulation

Se Hee Ahn, Se‐Kyeong Jang, Yu Jin Kim, Gyeongmi Kim, Ki Soo Park, In‐Chul Park, Hyeon‐Ok Jin
  • Cell Biology
  • Clinical Biochemistry
  • Genetics
  • Molecular Biology
  • Biochemistry
Show PDF Cite

Abstract

Thioredoxin‐interacting protein (TXNIP) is sensitive to oxidative stress and is involved in the pathogenesis of various metabolic, cardiovascular, and neurodegenerative disorders. Therefore, several studies have suggested that TXNIP is a promising therapeutic target for several diseases, particularly cancer and diabetes. However, the regulation of TXNIP expression under amino acid (AA)‐restricted conditions is not well understood. In the present study, we demonstrated that TXNIP expression was promoted by the deprivation of AAs, especially arginine, glutamine, lysine, and methionine, in non‐small cell lung cancer (NSCLC) cells. Interestingly, we determined that increased TXNIP expression induced by AA deprivation was associated with nuclear factor erythroid 2‐related factor 2 (NRF2) downregulation, but not with activating transcription factor 4 (ATF4) activation. Furthermore, N‐acetyl‐

l
‐cysteine (NAC), a scavenger of reactive oxygen species (ROS), suppressed TXNIP expression in NSCLC cells deprived of AA. Collectively, the induction of TXNIP expression by AA deprivation was mediated by ROS production, potentially through NRF2 downregulation. Our findings suggest that TXNIP expression may be associated with the redox homeostasis of AA metabolism and provide a possible rationale for a therapeutic strategy to treat cancer with AA restriction.

More from our Archive