Abstract

Cyclophosphamide (CYL) is a chemotherapeutic medication commonly used in managing various malignancies like breast cancer or leukemia. Though, CYL has been documented to induce lung toxicity. Mechanism of CYL toxicity is through oxidative stress and the release of damage-associated molecular patterns (DAMPs). Sesamol (SES) is a natural antioxidant isolated from Sesamum indicum and its effect against CYL-induced lung toxicity is not studied yet. This study aims to investigate whether SES could prevent any deleterious effects induced by CYL on lung using normal human lung cells, WI-38 cell line, without suppressing its efficacy. Cells were pretreated with SES and/or CYL for 24 h, then cell viability was estimated by MTS and trypan blue assays. The mode of cell death was determined by AO/EB staining. Additionally, caspase-3 level, oxidative stress, and inflammatory markers were evaluated by colorimetric and ELISA techniques. qRT-PCR was performed to evaluate RAGE, NF-κB, and Beclin-1 mRNA-expression. CYL-treated WI-38 cells developed a significantly increased cell death with enhanced oxidative and RAGE/NF-κb/Autophagy signaling, which were all attenuated after pretreatment with SES. Thus, we concluded that SES offered a protective role against CYL-induced lung injury via suppressing oxidative stress and RAGE/NF-κB/Autophagy signaling, which is a natural safe therapeutic option against CYL toxicities.Graphic

Highlights

  • Cyclophosphamide (CYL) is one of the commonly chemotherapeutic alkylating agents used in treating different types of malignancies including solid tumors and hematological malignancies in addition to treating several autoimmune diseases due to its immunosuppressive properties [1]

  • High mobility group box 1 (HMGB1), one of damage-associated molecular patterns (DAMPs), plays an essential role in activating inflammatory signaling due to CYL as a result of activating the receptor for advanced glycation end-products (RAGE) [8, 9]

  • Among the autophagy-related genes (Atg), Beclin 1, which is a main regulator of autophagy and it has a role in the formation of autophagosomes [13]

Read more

Summary

Introduction

Cyclophosphamide (CYL) is one of the commonly chemotherapeutic alkylating agents used in treating different types of malignancies including solid tumors and hematological malignancies in addition to treating several autoimmune diseases due to its immunosuppressive properties [1]. Phosphoramide is the active anticancer agent that acts on seven-guanine residues of DNA resulting in cancer cell death, whereas CYL-induced toxicity is in consequence of the formation of acrolein toxic metabolite [6, 7]. High mobility group box 1 (HMGB1), one of damage-associated molecular patterns (DAMPs), plays an essential role in activating inflammatory signaling due to CYL as a result of activating the receptor for advanced glycation end-products (RAGE) [8, 9]. A type II programmed cell death, is activated in stressful conditions such as starvation and exposure to chemotherapeutic drugs [12]. It is a dynamic process controlled by autophagy-related genes (Atg) to maintain normal cellular homeostasis by removing damaged organelles and proteins. The cytosolic form of the microtubule-associated protein light chain 3 (LC3)-I is conjugated to form LC3-II as an early autophagy marker [14]

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call