Modulation of Nrf2/HO-1 by Natural Compounds in Lung Cancer

Author:

Ghareghomi Somayyeh1ORCID,Moosavi-Movahedi Faezeh1,Saso Luciano2ORCID,Habibi-Rezaei Mehran34ORCID,Khatibi Ali5,Hong Jun6ORCID,Moosavi-Movahedi Ali A.17

Affiliation:

1. Institute of Biochemistry and Biophysics, University of Tehran, Tehran 1417466191, Iran

2. Department of Physiology and Pharmacology “Vittorio Erspamer”, Sapienza University of Rome, 00185 Rome, Italy

3. School of Biology, College of Science, University of Tehran, Tehran 1417466191, Iran

4. Center of Excellence in NanoBiomedicine, University of Tehran, Tehran 1417466191, Iran

5. Department of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran 1993893973, Iran

6. School of Life Sciences, Henan University, Kaifeng 475000, China

7. UNESCO Chair on Interdisciplinary Research in Diabetes, University of Tehran, Tehran 1417466191, Iran

Abstract

Oxidative stresses (OSs) are considered a pivotal factor in creating various pathophysiological conditions. Cells have been able to move forward by modulating numerous signaling pathways to moderate the defects of these stresses during their evolution. The company of Kelch-like ECH-associated protein 1 (Keap1) as a molecular sensing element of the oxidative and electrophilic stress and nuclear factor erythroid 2 (NF-E2)-related factor 2 (Nrf2) as a master transcriptional regulator of the antioxidant response makes a master cytoprotective antioxidant pathway known as the Keap1/Nrf2 pathway. This pathway is considered a dual-edged sword with beneficial features for both normal and cancer cells by regulating the gene expression of the array of endogenous antioxidant enzymes. Heme oxygenase-1 (HO-1), a critical enzyme in toxic heme removal, is one of the clear state indicators for the duality of this pathway. Therefore, Nrf2/HO-1 axis targeting is known as a novel strategy for cancer treatment. In this review, the molecular mechanism of action of natural antioxidants on lung cancer cells has been investigated by relying on the Nrf2/HO-1 axis.

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

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