Bisphenol-A/Radiation mediated inflammatory response activates EGFR/KRAS/ERK1/2 signaling pathway leads to lung carcinogenesis incidence.
Omayma Ar Abo-ZaidFatma S M MoawedHend A HassanEnas Mahmoud MoustafaPublished in: International journal of immunopathology and pharmacology (2022)
It was found that BPA and IR possess a harmful effect on the lungs via induction of oxidative stress, confirmed by increasing levels of malondialdehyde (MDA), nitric oxide, myeloperoxidase (MPO), and lactate dehydrogenase (LDH). Exposure to BPA and IR activates inflammatory cytokines TNF-α, IL-6, IL-1β, growth factors such as TGF-β, and gastrin-releasing peptides. BPA/IR exposures induced phosphorylated expression p-ERK1/2 and p-MEK1/2 associated with triggering of the GPER/EGFR/KRAS signaling factors, resulting in matrix metalloproteinase-2 and 9 overexpression and the development of lung tumors. Our findings support the causal role of two deleterious environmental pollutants BPA and IR, via the cytotoxicity in the respiratory system in the form of severe lung damage resulting in cancerous cells.
Keyphrases
- signaling pathway
- pi k akt
- induced apoptosis
- cell cycle arrest
- oxidative stress
- small cell lung cancer
- inflammatory response
- nitric oxide
- cell proliferation
- diabetic rats
- epidermal growth factor receptor
- tyrosine kinase
- rheumatoid arthritis
- endoplasmic reticulum stress
- breast cancer cells
- early onset
- transcription factor
- lps induced
- endothelial cells
- heat stress
- human health