Abstract

The effect of Eruca sativa seed extract (SE) on nuclear factor kappa B (NF-κB), cyclooxygenase-2 (COX-2) and B-cell lymphoma-2 (Bcl-2) gene expression levels was investigated in rat mammary gland carcinogenesis induced by 7,12 dimethylbenz(α)anthracene (DMBA). DMBA increased NF-κB, COX-2 and Bcl-2 gene expression levels and lipid peroxidation (LP), while, decreased glutathione-S-transferase (GST) and superoxide dismutase (SOD) activities and total antioxidant concentration (TAC) compared to the control group. After DMBA administration, SE treatment reduced NF-κB, COX-2 and Bcl-2 gene expression levels and LP. Hence, SE treatment reduced inflammation and cell proliferation, while increasing apoptosis, GST and SOD activities and TAC. Analysis revealed that SE has high concentrations of total flavonoids, triterpenoids, alkaloids and polyphenolic compounds such as gallic, chlorogenic, caffeic, 3,4-dicaffeoyl quinic, 3,5-dicaffeoyl quinic, tannic, cinnamic acids, catechin and phloridzin. These findings indicate that SE may be considered a promising natural product from cruciferous vegetables against breast cancer, especially given its high antioxidant properties.

Highlights

  • Breast cancer is the second most common cancer in the world

  • The results showed that the treatment with seed extract (SE) after DMBA (D-SE group) decreased the tumor volume significantly by 99.9% compared to the D group (Figure 2B)

  • The results of the present study revealed that DMBA administration increased tumor incidence and tumor volume

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Summary

Introduction

Breast cancer is the second most common cancer in the world. The most common types of breast cancer are ductal and lobular carcinoma (Zeeneldin et al, 2013). Environmental toxic agents especially polycyclic aromatic hydrocarbons (PAHs) are considered risk factors for breast cancer. Some of them are used in the industries of dyes, plastics and pesticides (Reynaud and Deschaux, 2006). They have carcinogenic and mutagenic effects since they alter the function of cell membranes and the associated enzyme systems. The most extensively studied PAHs are 7, 12-dimethylbenzo anthracene (DMBA) and benzo(a)pyrene. DMBA is an immunosuppressor and a powerful organ-specific laboratory carcinogen, it serves as a tumor initiator (Saha and Hait, 2012)

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