Effects of electromagnetic field, cisplatin and morphine on cytotoxicity and expression levels of DNA repair genes.
Fatemeh Sanie-JahromiMostafa HadatPublished in: Molecular biology reports (2018)
Morphine (Mor) is widely used as an analgesic drug in cancers and in combination with chemotherapy is known to have DNA damaging effects on non-targeted cell. This study surveyed the effect of Mor in combination with 50-Hz electromagnetic field (EMF) and co-treatment of cisplatin in combination with Mor and EMF on the expression of genes involved in DNA repair pathways. MCF-7 and SH-SY5Y cells were treated with 5.0 µM Mor and then exposed to 50-Hz 0.50 mT EMF in the intermittent pattern of 15 min field-on/15 min field-off. Gene expression, cisplatin and bleomycin cytotoxicity were measured using real-time PCR and MTT assay. Mor treated cells showed significant down-regulation of the examined genes, while in "Mor + EMF" treatments the genes were not significantly changed. IC50 of cisplatin was significantly elevated in both cell lines when co-treated with "Mor + EMF" compared with Mor treated cells. Non-homologous end joining (NHEJ) related genes were significantly decreased in co-treatment of cisplatin and "Mor + EMF" which led to bleomycin higher cytotoxicity in SH-SY5Y not in MCF-7. Our data is promising for providing a cell line-specific sensitization by combination of cisplatin and "Mor + EMF" treatment with local administration of double strand breaking agents.
Keyphrases
- dna repair
- induced apoptosis
- dna damage
- gene expression
- cell cycle arrest
- poor prognosis
- genome wide
- dna damage response
- dna methylation
- emergency department
- oxidative stress
- high frequency
- breast cancer cells
- machine learning
- mesenchymal stem cells
- bone marrow
- binding protein
- radiation therapy
- rectal cancer
- drug delivery
- big data
- spinal cord injury
- circulating tumor
- young adults
- pulmonary fibrosis
- replacement therapy