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Co-targeting PLK1 and mTOR induces synergistic inhibitory effects against esophageal squamous cell carcinoma.

Ting-Ting LiuKai-Xia YangJing YuYing-Ya CaoJian-Song RenJia-Jie HaoBei-Qing PanSai MaLi-Yan YangYan CaiMing-Rong WangYu Zhang
Published in: Journal of molecular medicine (Berlin, Germany) (2018)
PLK1 potentiates both mTORC1 and mTORC2 activities in ESCC cells. PLK1 expression positively correlated with mTOR activity in a subset of ESCC. Co-targeting of PLK1 and mTOR produced stronger antitumor effects partially due to synergistic inhibition of AKT, 4E-BP1 and S6 through cooperatively blocking mTORC2 and mTORC1 cascades. Combination targeting of PLK1 and mTOR may be a novel and promising therapeutic strategy for ESCC treatment.
Keyphrases
  • cancer therapy
  • cell proliferation
  • induced apoptosis
  • poor prognosis
  • drug delivery
  • signaling pathway
  • binding protein
  • long non coding rna
  • cell death
  • pi k akt
  • combination therapy
  • smoking cessation