Effects of electromagnetic field, cisplatin and morphine on cytotoxicity and expression levels of DNA repair genes

被引:0
作者
Fatemeh Sanie-Jahromi
Mostafa Saadat
机构
[1] Shiraz University,Department of Biology, College of Sciences
来源
Molecular Biology Reports | 2018年 / 45卷
关键词
Electromagnetic field; Cisplatin; Morphine; NHEJ; BER; NER; Gene expression;
D O I
暂无
中图分类号
学科分类号
摘要
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.
引用
收藏
页码:807 / 814
页数:7
相关论文
共 142 条
  • [1] Pang L(2002)ELF-electromagnetic fields inhibit the proliferation of human cancer cells and induce apoptosis Electromagn Biol Med 21 243-248
  • [2] Traitcheva N(2009)Electromagnetic effects—from cell biology to medicine Prog Histochem Cytochem 43 177-264
  • [3] Gothe G(2016)Extremely low frequency electromagnetic field sensitizes cisplatin-resistant human ovarian adenocarcinoma cells via P53 activation Cytotechnology 68 1403-1413
  • [4] Camacho Gomez JA(2007)Extremely low frequency electromagnetic fields prevent chemotherapy induced myelotoxicity Electromagn Biol Med 26 277-281
  • [5] Berg H(2013)Extremely low-frequency magnetic field enhances the therapeutic efficacy of low-dose cisplatin in the treatment of Ehrlich carcinoma Biomed Res Int 2013 189352-378
  • [6] Funk RHW(2014)Cisplatin in cancer therapy: molecular mechanisms of action Eur J Pharmacol 740 364-9
  • [7] Monsees T(2012)Mechanisms in cancer-chemotherapeutic drugs-induced peripheral neuropathy Toxicology 291 1-400
  • [8] Özkucur N(2007)Current aproach to cancer pain management: availability and implications of different treatment options Ther Clin Risk Manag 3 381-E360
  • [9] Baharara J(2011)Pharmacology of opioids in the treatment of chronic pain syndromes Pain Physician 14 E343-429
  • [10] Hosseini N(2016)Enhancement of cisplatin nephrotoxicity by morphine and its attenuation by the opioid antagonist naltrexone Acta Med Iran 54 422-341