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

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 cance...

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Detalles Bibliográficos
Autores principales: Bi, Ling, Xie, Chanlu, Jiao, Lijing, Jin, Shenyi, Hnit, Su Su Thae, Mu, Yao, Wang, Yilun, Wang, Qian, Ge, Guangbo, Wang, Yaqiao, Zhao, Xiaodong, Shi, Xinglong, Kang, Yani, De Souza, Paul, Liu, Tao, Zhou, Jia, Xu, Ling, Dong, Qihan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011132/
https://www.ncbi.nlm.nih.gov/pubmed/31960591
http://dx.doi.org/10.1111/jcmm.14897
Descripción
Sumario: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.