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Short Communication Open Access
Volume 3 | Issue 2 | DOI: https://doi.org/10.46439/cancerbiology.3.44

The intrinsically disordered DPF3 zinc finger protein: a promising new target in cancer therapy

  • 1Laboratoire de Chimie Physique des Biomolécules, UCPTS, Chemistry Department, University of Namur, 61 rue de Bruxelles, 5000 Namur, Belgium
  • 2Namur Institute of Structured Matter (NISM), University of Namur, Namur, Belgium
  • 3Namur Research Institute for Life Sciences (NARILIS), University of Namur, Namur, Belgium
+ Affiliations - Affiliations

Corresponding Author

Julien Mignon, julien.mignon@unamur.be

Received Date: October 20, 2022

Accepted Date: November 10, 2022

Abstract

Cancer is a worldwide human disease of great concern, in which proteins are known to be highly involved, especially the group of intrinsically disordered proteins (IDPs). Due to their disorder-associated properties and floppy structure, IDPs remain difficult to target, requiring the design of new anticancer strategies. In that context, the zinc finger protein DPF3 has been identified as an amyloidogenic IDP involved in numerous cancer types, such as breast, brain, bone marrow, kidney, and lung cancer. Therefore, investigating DPF3 druggability will help to elucidate its oncogenic mechanisms, as well as to pave the way towards efficient IDP-specific therapies. 

Keywords

Double PHD fingers 3 (DPF3); Intrinsically disordered protein; Cancer; Drug design; Protein aggregation; Amyloid fibril

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