2019
DOI: 10.1007/s00210-019-01652-z
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Radioprotective efficacy of dieckol against gamma radiation-induced cellular damage in hepatocyte cells

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Cited by 8 publications
(6 citation statements)
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“…Lastly, Xu and co-workers proved that 4 could be used to treat pancreatic cancer since it increased the expression of proapoptotic protein (Bax) and decreased antiapoptotic Bcl2 protein as well as cyclin D1, whose overexpression is often related to chemoresistance [109]. Finally, deickol (4) was found to provide the protection from gamma radiation and consequent damage, both in vitro and in vivo [110,111].…”
Section: Phlorotanninsmentioning
confidence: 99%
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“…Lastly, Xu and co-workers proved that 4 could be used to treat pancreatic cancer since it increased the expression of proapoptotic protein (Bax) and decreased antiapoptotic Bcl2 protein as well as cyclin D1, whose overexpression is often related to chemoresistance [109]. Finally, deickol (4) was found to provide the protection from gamma radiation and consequent damage, both in vitro and in vivo [110,111].…”
Section: Phlorotanninsmentioning
confidence: 99%
“…and PANC-1 (pancreatic cancer) cells [105,109] Protective and chemopreventing effects against hepatocellular carcinoma (HCC) in rats via upregulation of VEGF, MMP-2/9, PCNA and COX-2 [106,107] Anti-migratory and apoptotic activity in A549 cells associated with inhibition of Pi3K/AKT/mTOR signalling pathways and activation of tumor-suppressor, E-cadherin [108] Protection from gamma radiation and consequent damage, both in vitro and in vivo [110,111] Diphlorethohydroxycarmalol 5…”
Section: Eckolmentioning
confidence: 99%
“…From the results, it has been confirmed that eckol pretreatment efficiently scavenged ROS in gamma-irradiated V79-4 cells, protecting against DNA damage by decreasing oxidative damage. Sadeeshkumar et al [64] tested the radioprotective activity of dieckol in γ radiation-induced rat primary hepatocytes. Rat treated with dieckol showed reduced γ radiation-induced toxicity and enhanced the antioxidant activity, as well as decreased DNA damage and inflammation in hepatocyte cells.…”
Section: Dieckolmentioning
confidence: 99%
“…For instance, superoxide dismutase (SOD) and catalase (CAT), which are two important detoxifying enzymes that are usually downregulated in cells under oxidative stress, were shown to be increased on different cell lines treated either with phlorotannin-rich extracts (from F. vesiculosus , F. serratus , Pelvetia canaliculata and A. nodosum ) [ 43 , 51 , 52 ] or isolated phlorotannin compounds including phloroglucinol, eckol, eckstolonol, dieckol and triphlorethol A [ 31 , 32 , 48 , 49 , 68 , 69 , 70 ]. Likewise, glutathione (GSH), GSH peroxidase (GPx), GSH reductase (GR) and GSH-S-transferase (GST), which are crucial players in the neutralization of ROS and intimately associated to the maintenance of the redox balance in living organisms, were reported in multiple studies to be upregulated in response to the treatment of A. nodosum , H. elongata , F. serratus , F. vesiculosus , Pelvetia canaliculata , E. cava and Eisenia bicyclis phlorotannin extracts [ 45 , 50 , 51 , 71 ] as well as to phloroglucinol, triphlorethol A, eckol, phlorofucofuroeckol A, 7-phloroeckol and 6,6′-bieckol [ 31 , 34 , 65 , 70 , 72 ]. As reported by the authors, it is possible that phlorotannins may interfere with the transcriptional activity of the nuclear factor erythroid 2-related factor 2 (Nrf2), which is the major regulator of the phase II detoxifying enzymes [ 73 ].…”
Section: The Contribution Of Phlorotanninsmentioning
confidence: 99%
“…Similar observations were described for phlorofucofuroeckol A, which inhibited the phosphorylation of p38, ERK and JNK in LPS-stimulated Raw 264.7 cells [ 96 ], and for phloroglucinol, which blocked the phosphorylation of ERK in HT1080 cells [ 54 ], both resulting in the suppression of AP-1 activity, another transcription factor involved in the regulation of some pro-inflammatory mediators such as matrix metalloproteinases, a group of enzymes involved in the tissue remodeling during chronic inflammation and cell motility further in a tumor environment. The inhibitory effects of these and other isolated phlorotannins such as eckol, eckstolonol, 6,6′-bieckol, 8,8′-bieckol, fucofuroeckol-A over NF-κB and MAPKs have been reported in multiple cell lines elicited with different pro-inflammatory stimulus, including LPS-induced BV2 microglia cells, THP-1 or Raw 264.7 macrophages, Aβ 25–35 -stimulated PC12 pheochromocytoma cells, PMA-induced MG-63 human osteosarcoma cells, high glucose-induced HUVEC endothelial cells, hypoxia-induced primary mouse hepatocytes and gamma-irradiated primary rat hepatocytes [ 46 , 65 , 81 , 82 , 88 , 89 , 106 , 109 , 110 , 111 , 112 ], suggesting that these compounds may act in a wide range of inflammatory conditions.…”
Section: The Contribution Of Phlorotanninsmentioning
confidence: 99%