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The interaction between S100A2 and KPNA2 mediates NFYA nuclear import and is a novel therapeutic target for colorectal cancer metastasis.

Fengyan HanLei ZhangShaoxia LiaoYanmin ZhangLili QianFeijun HouJingwen GongMaode LaiHonghe Zhang
Published in: Oncogene (2021)
Nucleocytoplasmic transport of proteins is disrupted and dysregulated in cancer cells. Nuclear pore complexes and cargo proteins are two main transportation regulators. However, the mechanism regulating nucleocytoplasmic transport in cancer remains elusive. Here, we identified a S100A2/KPNA2 cotransport complex that transports the tumor-associated transcription factor NFYA in colorectal cancer (CRC). Through the S100A2/KNPA2 complex, depending on its interaction with S100A2, NFYA is transported to the nucleus and inhibits the transcriptional activity of E-cadherin, which in turn promotes CRC metastasis. Targeting the S100A2/KPNA2 binding sites with the specific inhibitor delanzomib is a potential therapeutic approach for CRC.
Keyphrases
  • transcription factor
  • papillary thyroid
  • dna binding
  • gene expression
  • sensitive detection
  • squamous cell
  • fluorescent probe
  • living cells
  • squamous cell carcinoma
  • oxidative stress
  • heat shock
  • quantum dots