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Author Notes:

Correspondence to: Jing Chen (jchen@emory.edu), Hualiang Jiang (hljiang@mail.shcnc.ac.cn), or Chuan He (chuanhe@uchicago.edu).

C.H. conceived the project with H.J. and J.C., and J.W., C.Luo, C.S. and Q.Y. designed and performed most of the experiments.

J.L. and S.O. performed the virtual screening and bioinformatics analysis.

S.E., J.F. and H.K. assisted with the cell and mice experiments.

Y.Z. and H.L. assisted in the synthesis of the compounds.

J.L.V. and M.M. assisted in setting up the FRET-based compound screening, Y.W. and N.Z. conducted the NMR experimental and data analysis of DC_AC2 with Atox1.

C.Luan, H.D. and S.C. performed the SPR experiments for DC_AC50 with Atox1 and CCS.

C.H. and J.W. wrote the manuscript with input from H.J. and J.C.

We thank S. F. Reichard for help with editing the manuscript.

Competing financial interests: A patent application on DC_AC50 has been filed by the University of Chicago and the Shanghai Institute of Materia Medica.

Subjects:

Research Funding:

This work was supported by grants from the National Natural Science Foundation of China (21210003 to H.J. and C.H., and 81230076, 91313000 to H.J.), the Hi-Tech Research and Development Program of China (2012AA020302 and 2012AA01A305 to C.L.), Chinese Academy of Sciences (XDA01040305 to C.L.), National Science Foundation (CHE-1213598 to C.H.) and National Institutes of Health (CA140515 to J.C.).

C.H. is supported by the Howard Hughes Medical Institute as an investigator.

Keywords:

  • Science & Technology
  • Physical Sciences
  • Chemistry, Multidisciplinary
  • Chemistry
  • SUPEROXIDE-DISMUTASE
  • ANTICANCER STRATEGY
  • OXIDATIVE STRESS
  • METALLOCHAPERONE
  • METABOLISM
  • CHAPERONE
  • HOMEOSTASIS
  • MECHANISMS
  • DISEASE
  • TARGET

Inhibition of human copper trafficking by a small molecule significantly attenuates cancer cell proliferation

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Journal Title:

Nature Chemistry

Volume:

Volume 7, Number 12

Publisher:

, Pages 968-979

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Copper is a transition metal that plays critical roles in many life processes. Controlling the cellular concentration and trafficking of copper offers a route to disrupt these processes. Here we report small molecules that inhibit the human copper-trafficking proteins Atox1 and CCS, and so provide a selective approach to disrupt cellular copper transport. The knockdown of Atox1 and CCS or their inhibition leads to a significantly reduced proliferation of cancer cells, but not of normal cells, as well as to attenuated tumour growth in mouse models. We show that blocking copper trafficking induces cellular oxidative stress and reduces levels of cellular ATP. The reduced level of ATP results in activation of the AMP-activated protein kinase that leads to reduced lipogenesis. Both effects contribute to the inhibition of cancer cell proliferation. Our results establish copper chaperones as new targets for future developments in anticancer therapies.

Copyright information:

© 2015 Macmillan Publishers Limited.

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