The Nrf2/HO-1 Axis in Cancer Cell Growth and Chemoresistance

Author:

Furfaro A. L.1,Traverso N.2,Domenicotti C.2,Piras S.2,Moretta L.3,Marinari U. M.2,Pronzato M. A.2,Nitti M.2

Affiliation:

1. Giannina Gaslini Institute, Via Gerolamo Gaslini 5, 16147 Genoa, Italy

2. Department of Experimental Medicine, University of Genoa, Via L. B. Alberti 2, 16132 Genoa, Italy

3. Bambino Gesù Children’s Hospital, IRCCS, Piazza S. Onofrio 4, 00165 Rome, Italy

Abstract

The transcription factor, nuclear factor erythroid 2 p45-related factor 2 (Nrf2), acts as a sensor of oxidative or electrophilic stresses and plays a pivotal role in redox homeostasis. Oxidative or electrophilic agents cause a conformational change in the Nrf2 inhibitory protein Keap1 inducing the nuclear translocation of the transcription factor which, through its binding to the antioxidant/electrophilic response element (ARE/EpRE), regulates the expression of antioxidant and detoxifying genes such as heme oxygenase 1 (HO-1). Nrf2 and HO-1 are frequently upregulated in different types of tumours and correlate with tumour progression, aggressiveness, resistance to therapy, and poor prognosis. This review focuses on the Nrf2/HO-1 stress response mechanism as a promising target for anticancer treatment which is able to overcome resistance to therapies.

Funder

MIUR-PRIN

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

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