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Targeting of RRM2 suppresses DNA damage response and activates apoptosis in atypical teratoid rhabdoid tumor.

Le Hien GiangKuo-Sheng WuWei-Chung LeeShing-Shung ChuAnh Duy DoChun A ChangouHuy Minh TranTsung-Han HsiehHsin-Hung ChenChia-Ling HsiehShian-Ying SungAlice L YuYun YenTai-Tong WongChe-Chang Chang
Published in: Journal of experimental & clinical cancer research : CR (2023)
Collectively, our study uncovers the oncogenic functions of RRM2 in ATRT cell lines, and highlights the therapeutic potential of targeting RRM2 in ATRT. The promising effect of COH29 on ATRT suggests its potential suitability for clinical trials as a novel therapeutic approach for ATRT.
Keyphrases
  • dna damage response
  • clinical trial
  • cancer therapy
  • oxidative stress
  • dna repair
  • signaling pathway
  • cell death
  • transcription factor
  • cell cycle arrest
  • randomized controlled trial
  • phase ii
  • study protocol