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An antisense amido-bridged nucleic acid gapmer oligonucleotide targeting SRRM4 alters REST splicing and exhibits anti-tumor effects in small cell lung cancer and prostate cancer cells.

Misa YoshidaChihiro OdaKeishiro MishimaItsuki TsujiSatoshi ObikaMasahito Shimojo
Published in: Cancer cell international (2023)
Our data demonstrate that a gapmer ASO targeting SRRM4 (SRRM4 ASO) reduces cell viability through splicing changes of REST, followed by affecting REST-controlled genes in recalcitrant tumors SCLC and PCa cells.
Keyphrases
  • nucleic acid
  • small cell lung cancer
  • induced apoptosis
  • cancer therapy
  • cell cycle arrest
  • genome wide
  • big data
  • endoplasmic reticulum stress
  • cell death
  • dna methylation
  • data analysis
  • transcription factor
  • pi k akt