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Silver nanoparticles protect human keratinocytes against UVB radiation-induced DNA damage and apoptosis: potential for prevention of skin carcinogenesis

机译:银纳米颗粒保护人类角质形成细胞免受UVB辐射诱导的DNA损伤和细胞凋亡:预防皮肤癌变的潜力

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摘要

Ultraviolet (UV)-B radiation from the sun is an established etiological cause of skin cancer, which afflicts more than a million lives each year in the United States alone. Here, we tested the chemopreventive efficacy of silver-nanoparticles (AgNPs) against UVB-irradiation-induced DNA damage and apoptosis in human immortalized keratinocytes (HaCaT). AgNPs were synthesized by reduction-chemistry and characterized for their physicochemical properties. AgNPs were well tolerated by HaCaT cells and their pretreatment protected them from UVB-irradiation-induced apoptosis along with significant reduction in cyclobutane-pyrimidine-dimer formation. Moreover, AgNPs pre-treatment led to G1-phase cell-cycle arrest in UVB-irradiated HaCaT cells. AgNPs were efficiently internalized in UVB-irradiated cells and localized into cytoplasmic and nuclear compartments. Furthermore, we observed an altered expression of various genes involved in cell-cycle, apoptosis and nucleotide-excision repair in HaCaT cells treated with AgNPs prior to UVB-irradiation. Together, these findings provide support for potential utility of AgNPs as novel chemopreventive agents against UVB-irradiation-induced skin carcinogenesis.
机译:来自太阳的紫外线(UV)-B辐射是皮肤癌的既定病因,每年仅在美国就折磨一百万以上的生命。在这里,我们测试了银纳米颗粒(AgNPs)对人类永生化角质形成细胞(HaCaT)中UVB辐射诱导的DNA损伤和细胞凋亡的化学预防功效。 AgNPs通过还原化学合成,并对其理化性质进行了表征。 AgNPs被HaCaT细胞很好地耐受,它们的预处理可以保护它们免受UVB辐射诱导的细胞凋亡以及环丁烷-嘧啶-二聚体形成的显着减少。此外,AgNPs预处理导致UVB照射的HaCaT细胞中G1期细胞周期停滞。 AgNP被有效地内在UVB照射的细胞中,并定位在细胞质和核区室中。此外,我们观察到在紫外线照射之前,用AgNPs处理的HaCaT细胞中参与细胞周期,凋亡和核苷酸切除修复的各种基因的表达发生了变化。在一起,这些发现为AgNPs作为新型化学预防剂针对UVB辐射诱导的皮肤癌变提供了潜在的支持。

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