HMQ-T-F2 exert antitumour effects by upregulation of Axin in human cervical HeLa cells

J Cell Mol Med. 2018 May;22(5):2955-2959. doi: 10.1111/jcmm.13577. Epub 2018 Mar 7.

Abstract

Looking for novel, effective and less toxic therapies for cervical cancer is of significant importance. In this study, we reported that HMQ-T-F2(F2) significantly inhibited cell proliferation and transplantable tumour growth. Mechanistically, HMQ-T-F2 inhibited HeLa cell growth through repressing the expression and nuclear translocation of β-catenin, enhancing Axin expression, as well as downregulating the Wnt downstream targeted proteins. Knock-down of a checkpoint β-catenin by siRNA significantly attenuated HeLa cell proliferation. Furthermore, XAV939, an inhibitor of β-catenin, was used to treat HeLa cells and the results demonstrated that HMQ-T-F2 inhibited proliferation and migration via the inhibition of the Wnt/β-catenin pathway.

Keywords: HMQ-T-F2; Wnt/β-catenin signal; cervical HeLa cells; proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axin Protein / genetics
  • Axin Protein / metabolism
  • Cell Proliferation / drug effects
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • HeLa Cells
  • Humans
  • Mice
  • Thiourea / pharmacology*
  • Transcriptional Activation / genetics
  • Up-Regulation / drug effects*
  • Uterine Cervical Neoplasms / genetics*
  • Uterine Cervical Neoplasms / pathology
  • beta Catenin / metabolism

Substances

  • Axin Protein
  • beta Catenin
  • Thiourea