Leichner Jared, Sarwar Mehenur, Nilchian Amirali, Zhu Xuena, Liu Hongyun, Shuang Shaomin, Li Chen-Zhong
Nanobioengineering & Bioelectronics Lab, Department of Biomedical Engineering, Florida International University, 10555 West Flagler Street, Miami, FL, 33174, USA.
College of Chemistry, Beijing Normal University, Beijing, 100875, China.
Methods Mol Biol. 2017;1572:23-39. doi: 10.1007/978-1-4939-6911-1_3.
The phrase "oxidative-stress induced DNA damage" is commonly used in both the scientific literature and common media outlets, and is frequently linked to detrimental elements of aging as well as the onset of illnesses. Due to the growing focus on this topic, a clear need has emerged to develop a quantitative, low-cost methodology to allow for periodic monitoring of oxidative-stress induced DNA damage within individuals. Recent literature examining the link between oxidative stress and the onset of various cancers has made monitoring an even more pressing need. The mechanism of oxidative-stress induced DNA damage originates in chronic inflammation, which in turn activates various transcription factors and diseases that influence the onset of tumor development, chemoresistance, radioresistance, and other harmful cellular processes. While current technologies that aim to provide quantitative metrics require extremely expensive equipment and significant technical expertise, our laboratory has designed a low-cost methodology utilizing a combination of carbon nanotubes, paper electrodes, and immunochromatographic strips.
“氧化应激诱导的DNA损伤”这一表述在科学文献和大众媒体中都很常见,并且经常与衰老的有害因素以及疾病的发生联系在一起。由于对这一主题的关注度不断提高,迫切需要开发一种定量、低成本的方法,以便定期监测个体体内氧化应激诱导的DNA损伤。最近有关氧化应激与各种癌症发生之间联系的文献使监测需求变得更加紧迫。氧化应激诱导DNA损伤的机制源于慢性炎症,慢性炎症进而激活各种转录因子以及影响肿瘤发生、化疗耐药性、放疗耐受性和其他有害细胞过程的疾病。虽然目前旨在提供定量指标的技术需要极其昂贵的设备和大量的专业技术知识,但我们实验室设计了一种低成本方法,该方法利用了碳纳米管、纸质电极和免疫层析试纸条的组合。