Attenuation of Oxidative Damage via Upregulating Nrf2/HO-1 Signaling Pathway by Protease SH21 with Exerting Anti-Inflammatory and Anticancer Properties In Vitro

Cells. 2023 Sep 1;12(17):2190. doi: 10.3390/cells12172190.

Abstract

Oxidative damage and inflammation are among the very significant aspects interrelated with cancer and other degenerative diseases. In this study, we investigated the biological activities of a 25 kDa protease (SH21) that was purified from Bacillus siamensis. SH21 exhibited very powerful antioxidant and reactive oxygen species (ROS) generation inhibition activity in a dose-dependent approach. The mRNA and protein levels of antioxidant enzymes such as superoxide dismutase 1 (SOD1), catalase (CAT), and glutathione peroxidase 1 (GPx-1) were enhanced in the SH21-treated sample. SH21 also increased the transcriptional and translational activities of NF-E2-related factor 2 (Nrf2) with the subsequent development of detoxifying enzyme heme oxygenase-1 (HO-1). In addition, SH21 showed potential anti-inflammatory activity via inhibition of nitric oxide (NO) and proinflammatory cytokines, such as TNF-α, IL-6, and IL-1β, production in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. At concentrations of 60, 80, and 100 μg/mL, SH21 potentially suppressed nitric oxide synthase (iNOS) and cytokine gene expressions. Furthermore, SH21 significantly released lactate dehydrogenase (LDH) enzyme in cancer cell supernatant in a concentration-dependent manner and showed strong activity against three tested cancer cell lines, including HL-60, A549, and Hela. Our results suggest that SH21 has effective antioxidant, anti-inflammatory, and anticancer effects and could be an excellent therapeutic agent against inflammation-related diseases.

Keywords: anti-inflammatory; anticancer; antioxidants; oxidative damage; protease SH21.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endopeptidases
  • Heme Oxygenase-1
  • Humans
  • Inflammation / drug therapy
  • NF-E2-Related Factor 2*
  • Oxidative Stress
  • Peptide Hydrolases*
  • Signal Transduction

Substances

  • Endopeptidases
  • Heme Oxygenase-1
  • NF-E2-Related Factor 2
  • Peptide Hydrolases

Grants and funding

This work was sponsored by a research fund from Chosun University, 2023.