CPF impedes cell cycle re-entry of quiescent lung cancer cells through transcriptional suppression of FACT and c-MYC

J Cell Mol Med. 2020 Feb;24(3):2229-2239. doi: 10.1111/jcmm.14897. Epub 2020 Jan 20.

Abstract

Blockade of cell cycle re-entry in quiescent cancer cells is a strategy to prevent cancer progression and recurrence. We investigated the action and mode of action of CPF mixture (Coptis chinensis, Pinellia ternata and Fructus trichosanthis) in impeding a proliferative switch in quiescent lung cancer cells. The results indicated that CPF impeded cell cycle re-entry in quiescent lung cancer cells by reduction of FACT and c-MYC mRNA and protein levels, with concomitant decrease in H3K4 tri-methylation and RNA polymerase II occupancy at FACT and c-MYC promoter regions. Animals implanted with quiescent cancer cells that had been exposed to CPF had reduced tumour volume/weight. Thus, CPF suppresses proliferative switching through transcriptional suppression of FACT and the c-MYC, providing a new insight into therapeutic target and intervention method in impeding cancer recurrence.

Keywords: G0 cell cycle re-entry; c-MYC; lung cancer; structure-specific recognition protein 1; suppressor of Ty homolog-16.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Animals
  • Araceae / chemistry
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • DNA-Binding Proteins / genetics*
  • High Mobility Group Proteins / genetics*
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / genetics*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Plant Extracts / pharmacology*
  • Promoter Regions, Genetic / drug effects
  • Proto-Oncogene Proteins c-myc / genetics*
  • RNA, Messenger / genetics
  • Ranunculaceae / chemistry
  • Transcription, Genetic / drug effects*
  • Transcriptional Elongation Factors / genetics*
  • Trichosanthes / chemistry

Substances

  • DNA-Binding Proteins
  • High Mobility Group Proteins
  • MYC protein, human
  • Plant Extracts
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • SSRP1 protein, human
  • Transcriptional Elongation Factors