首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Formaldehyde-induced DNA adducts as biomarkers of in vitro human nasal epithelial cell exposure to formaldehyde.
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Formaldehyde-induced DNA adducts as biomarkers of in vitro human nasal epithelial cell exposure to formaldehyde.

机译:甲醛诱导的DNA加合物是体外人鼻上皮细胞暴露于甲醛的生物标记。

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Formaldehyde (FA) is a mutagen that, at high concentrations and long durations, has been reported to cause nasal cancer in rats and in some humans. The level of FA-induced modified DNA in nasal cells should serve as a biomarker of FA exposure and effect. In the present study, a high-performance liquid chromatography (HPLC)-ultraviolet (UV) method at 254 nm was developed and optimized to detect and quantify hydroxymethyldeoxynucleosides after the isolated DNA in exposed human nasal epithelial cells (HNEC) was enzymically digested. Normal and modified deoxynucleosides were successfully resolved from one another and from tissue and enzyme blank interferences. The viability of HNEC exposed to FA in solution for 24 h decreased, and there was a linear dose response between % nonviability and FA dose from 10 to 500 microg/mL. Amounts of 18.0 +/- 1.5 pmol N6-dA and 12.0 +/- 1.2 pmol N2-dG derivatives were determined in a 10 microL injection after 1.4 x 10(7) HNEC (106 microg DNA) were exposed to 500 microg/mL in solution. The respective tissue concentrations in pmol hydroxymethyldeoxynucleoside/mg DNA were 170 +/- 14 and 113 +/- 11. The lower quantifiable limits were about 97 and 88 pmol/mg DNA, respectively. Diffusive exposure of HNEC to air FA up to 100 ppm (v/v) for 24 h did not produce quantifiable hydroxymethylnucleosides. FA-modified deoxynucleosides may be useful biomarkers for FA exposure in biological monitoring samples taken by nasal lavage or brush biopsy.
机译:甲醛(FA)是一种诱变剂,在高浓度下且持续时间长,据报道会在大鼠和某些人类中引起鼻癌。鼻细胞中FA诱导的修饰DNA的水平应作为FA暴露和作用的生物标志物。在本研究中,开发了一种高效液相色谱(HPLC)-紫外(UV)方法在254 nm处进行了优化,以检测和量化暴露的人鼻上皮细胞(HNEC)中分离的DNA后羟甲基脱氧核苷的含量。正常的和修饰的脱氧核苷彼此之间以及与组织和酶的空白干扰之间已成功分离。在溶液中暴露于FA 24小时的HNEC的活力降低,并且%无活力和FA剂量在10至500 microg / mL之间存在线性剂量响应。在将1.4 x 10(7)HNEC(106 microg DNA)暴露于500 microg / mL的10μL注射液中后,以10 microL进样确定18.0 +/- 1.5 pmol N6-dA和12.0 +/- 1.2 pmol N2-dG衍生物的量。解。 pmol羟甲基脱氧核苷/ mg DNA的各自组织浓度分别为170 +/- 14和113 +/-11。可量化下限分别为约97和88 pmol / mg DNA。 HNEC在空气FA中扩散暴露至高达100 ppm(v / v)的时间达24小时,未产生可量化的羟甲基核苷。 FA修饰的脱氧核苷可能是有用的生物标志物,可用于通过洗鼻或刷式活检采集的生物监测样品中的FA暴露。

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