Unraveling the Potential Role of NEDD4-like E3 Ligases in Cancer

Int J Mol Sci. 2022 Oct 16;23(20):12380. doi: 10.3390/ijms232012380.

Abstract

Cancer is a deadly disease worldwide, with an anticipated 19.3 million new cases and 10.0 million deaths occurring in 2020 according to GLOBOCAN 2020. It is well established that carcinogenesis and cancer development are strongly linked to genetic changes and post-translational modifications (PTMs). An important PTM process, ubiquitination, regulates every aspect of cellular activity, and the crucial enzymes in the ubiquitination process are E3 ubiquitin ligases (E3s) that affect substrate specificity and must therefore be carefully regulated. A surfeit of studies suggests that, among the E3 ubiquitin ligases, neuronal precursor cell-expressed developmentally downregulated 4 (NEDD4)/NEDD4-like E3 ligases show key functions in cellular processes by controlling subsequent protein degradation and substrate ubiquitination. In addition, it was demonstrated that NEDD4 mainly acts as an oncogene in various cancers, but also plays a tumor-suppressive role in some cancers. In this review, to comprehend the proper function of NEDD4 in cancer development, we summarize its function, both its tumor-suppressive and oncogenic role, in multiple types of malignancies. Moreover, we briefly explain the role of NEDD4 in carcinogenesis and progression, including cell survival, cell proliferation, autophagy, cell migration, invasion, metastasis, epithelial-mesenchymal transition (EMT), chemoresistance, and multiple signaling pathways. In addition, we briefly explain the significance of NEDD4 as a possible target for cancer treatment. Therefore, we conclude that targeting NEDD4 as a therapeutic method for treating human tumors could be a practical possibility.

Keywords: E3 ligases; NEDD4; cancer; oncogene; targeted therapy; tumor suppressor; ubiquitination.

Publication types

  • Review

MeSH terms

  • Carcinogenesis
  • Endosomal Sorting Complexes Required for Transport / metabolism
  • Humans
  • Nedd4 Ubiquitin Protein Ligases / metabolism
  • Neoplasms* / pathology
  • Ubiquitin-Protein Ligases* / metabolism
  • Ubiquitination
  • Ubiquitins / metabolism

Substances

  • Ubiquitin-Protein Ligases
  • Nedd4 Ubiquitin Protein Ligases
  • Endosomal Sorting Complexes Required for Transport
  • Ubiquitins

Grants and funding

The author(s) disclose receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by the BT/556/NE/U-Excel/2016 grant awarded to Ajaikumar B. Kunnumakkara by the Department of Biotechnology (DBT), Government of India. The authors extend their appreciation to the Deanship of Scientific Research at King Khalid University (KKU) for funding this work through the Research Group Program under research project number (R.G.P.1/256/43). This work was supported by the Ministry of Education Tier 1 Grant (R-184-000-301-114) to Gautam Sethi.