Literature DB >> 28619596

Selective p300 inhibitor C646 inhibited HPV E6-E7 genes, altered glucose metabolism and induced apoptosis in cervical cancer cells.

Hongpeng He1, Yongwei Lai1, Yunpeng Hao1, Yupeng Liu1, Zijiang Zhang1, Xiang Liu1, Chenhong Guo1, Mengmeng Zhang1, Hao Zhou1, Nan Wang1, Xue-Gang Luo1, Lihong Huo1, Wenjian Ma1, Tong-Cun Zhang2.   

Abstract

High risk HPV infection is a causative factor of cervical cancer. The constitutive expression of HPV E6-E7 genes is important for the maintenance of cancer phenotypes. The cellular transcription co-activator p300 plays a crucial role in the regulation of HPV genes thus it was targeted for the inhibition of HPV-associated cervical cancer. In the present study, HPV positive cervical cells were treated with C646, a selective inhibitor of p300, to investigate its influence on HPV E6-E7 expression and cancer cell growth. Results of RT-qPCR, Western-blot and promoter activity assays showed that C646 inhibited the transcription of HPV E6-E7, which was accompanied with the accumulation of p53 protein. Meanwhile, cell proliferation was suppressed, glucose metabolism was disrupted and apoptosis was induced via the intrinsic pathway. Generally, the anti-cervical cancer potential of C646 was demonstrated and a novel mechanism was proposed in this study.
Copyright © 2017. Published by Elsevier B.V.

Entities:  

Keywords:  Cervical cancer; Glycolysis; HPV E6-E7; P300 inhibitor; P53 accumulation

Mesh:

Substances:

Year:  2017        PMID: 28619596     DOI: 10.1016/j.ejphar.2017.06.005

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  12 in total

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