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DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification.

Emma Tabe Eko NibaRyo YamanakaAbdul Qawee Mahyoob RaniHiroyuki AwanoMasaaki MatsumotoHisahide NishioMasafumi Matsuo
Published in: Cancer cell international (2017)
Intron-specific PCR amplification showed that DMD transcripts contained high levels of introns 40, 58 and 70. Retention of these introns may have been responsible for the lack of dystrophin expression by CRL-2061 cells, thereby abolishing the tumor suppressor activity of dystrophin.
Keyphrases
  • duchenne muscular dystrophy
  • induced apoptosis
  • muscular dystrophy
  • cell cycle arrest
  • oxidative stress
  • signaling pathway
  • cell death
  • real time pcr