Dysregulating ClpP: From Antibiotics to Anticancer?

Research output: Contribution to journalSurvey paperResearchpeer review

Authors

  • David A. Dougan
  • Ingo Hantke
  • Kürşad Turgay

Research Organisations

External Research Organisations

  • La Trobe University
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Details

Original languageEnglish
Pages (from-to)929-930
Number of pages2
JournalCell Chemical Biology
Volume25
Issue number8
Publication statusPublished - 16 Aug 2018

Abstract

In this issue of Cell Chemical Biology, Wong et al. (2018) identify several dysregulators of a key mitochondrial protease: casein lytic protease P (ClpP). These dysregulators were found to trigger programmed cell death and may offer fresh avenues for the development of novel cancer therapeutics.

Keywords

    Anti-Bacterial Agents, Caseins, Cell Death, Endopeptidase Clp, Humans, Mitochondria

ASJC Scopus subject areas

Sustainable Development Goals

Cite this

Dysregulating ClpP: From Antibiotics to Anticancer? / Dougan, David A.; Hantke, Ingo; Turgay, Kürşad.
In: Cell Chemical Biology, Vol. 25, No. 8, 16.08.2018, p. 929-930.

Research output: Contribution to journalSurvey paperResearchpeer review

Dougan, DA, Hantke, I & Turgay, K 2018, 'Dysregulating ClpP: From Antibiotics to Anticancer?', Cell Chemical Biology, vol. 25, no. 8, pp. 929-930. https://doi.org/10.1016/j.chembiol.2018.08.002
Dougan, D. A., Hantke, I., & Turgay, K. (2018). Dysregulating ClpP: From Antibiotics to Anticancer? Cell Chemical Biology, 25(8), 929-930. https://doi.org/10.1016/j.chembiol.2018.08.002
Dougan DA, Hantke I, Turgay K. Dysregulating ClpP: From Antibiotics to Anticancer? Cell Chemical Biology. 2018 Aug 16;25(8):929-930. doi: 10.1016/j.chembiol.2018.08.002
Dougan, David A. ; Hantke, Ingo ; Turgay, Kürşad. / Dysregulating ClpP : From Antibiotics to Anticancer?. In: Cell Chemical Biology. 2018 ; Vol. 25, No. 8. pp. 929-930.
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AU - Dougan, David A.

AU - Hantke, Ingo

AU - Turgay, Kürşad

N1 - Funding Information: I.H. and K.T. are supported by the Hannover School for Biomolecular Drug Research and the Deutsche Forschungsgemeinschaft . The authors declare no competing interests. Publisher Copyright: © Elsevier Ltd Copyright: Copyright 2018 Elsevier B.V., All rights reserved.

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