Correlation Engine 2.0
Clear Search sequence regions


  • bromide (1)
  • cell number (1)
  • colon cancer (6)
  • cordycepin (11)
  • cordyceps militaris (1)
  • humans (1)
  • miR 26a (6)
  • mirnas (1)
  • mirnas (3)
  • miRs (1)
  • mrna (1)
  • MYC (8)
  • western blot (1)
  • Sizes of these terms reflect their relevance to your search.

    Cordycepin is a purine nucleoside anti-metabolite and anti-biotic isolated from the fungus Cordyceps militaris, which has potential anti-neoplastic activities. This study aimed to investigate the effect of cordycepin in inhibiting colon cancer development. The proliferation of cordycepin-treated HCT116 and Caco-2 colon cancer cell lines was assessed with 3- (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and the viability was measured with colony formation assay. At the same time, cordycepin responsive gene and microRNAs (miRNAs, miRs) were screened by qRT-PCR. MYC over-expressing HCT116 and Caco-2 cell lines were constructed, which were further transfected with miR-26a. Inhibitory effect of cordycepin on cell proliferation was evaluated with cell viability assay, cell number count, and colony formation assay. The relative expression of MYC and miR-26a was detected by qRT-PCR and Western blot. Cordycepin inhibited colon cancer cell proliferation by down-regulating MYC mRNA/protein expression and up-regulating miR-26a in both HCT116 and Caco-2 cells. MYC over-expression could suppress the expression of miR-26a, which could be restored by cordycepin treatment. Additional miR-26a transfection in MYC over-expressing cells could reverse MYC over-expression-promoted proliferation, which could be further potentiated by cordycepin treatment. Cordycepin is able to suppress colon cancer cell proliferation, likely mediated by the MYC/miR-26a pathway, supporting its potential for the treatment of colon cancer. © 2022. The Author(s).

    Citation

    Zhe Zhang, Kui Li, Zhi Zheng, Yu Liu. Cordycepin inhibits colon cancer proliferation by suppressing MYC expression. BMC pharmacology & toxicology. 2022 Feb 04;23(1):12

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35120580

    View Full Text