Department of Nutritional Sciences, University of Wisconsin, Madison, WI 53706-1527, USA.
J Nutr Biochem. 2010 Aug;21(8):665-70. doi: 10.1016/j.jnutbio.2009.11.012. Epub 2010 Mar 20.
In medicine, mRNA transcripts are being developed as molecular biomarkers for the diagnosis and treatment of a number of diseases. These biomarkers offer early and more accurate prediction and diagnosis of disease and disease progression, and ability to identify individuals at risk. Use of microarrays also offers opportunity to identify orthogonal (uncorrelated) biomarkers not known to be linked with conventional biomarkers. Investigators are increasingly using blood as a surrogate tissue for biopsy and analysis; total RNA isolated from whole blood is predominantly from erythroid cells, and whole blood mRNA shares more than 80% of the transcriptome with major tissues. Thus blood mRNA biomarkers for individualized disease prediction and diagnosis are an exciting area in medicine; mRNA biomarkers in nutrition have potential application that parallels these opportunities. Assessment of selenium (Se) status and requirements is one area where tissue mRNA levels have been used successfully. Selenoprotein-H and selenoprotein-W as well as glutathione peroxidase-1 (Gpx1) mRNAs are highly down-regulated in Se deficiency in rat liver, and the minimum dietary Se requirement is 0.06-0.07 microg Se/g based on these biomarkers, similar to requirements determined using conventional biomarkers. Blood Gpx1 mRNA can also be used to determine Se requirements in rats, showing that blood mRNA has potential for assessment of nutrient status. Future research is needed to develop mRNA biomarker panels for all nutrients that will discriminate between deficient, marginal, adequate and supernutritional individuals and populations, and differentiate between individuals who will benefit vs. be adversely affected by nutrient supplementation.
在医学领域,mRNA 转录本被开发为多种疾病的诊断和治疗的分子生物标志物。这些生物标志物提供了疾病和疾病进展的早期、更准确的预测和诊断,并且能够识别出有风险的个体。微阵列的使用还提供了识别与传统生物标志物不相关的正交(不相关)生物标志物的机会。研究人员越来越多地将血液作为活检和分析的替代组织;从全血中分离的总 RNA 主要来自于红细胞,而全血 mRNA 与主要组织共享超过 80%的转录组。因此,用于个体化疾病预测和诊断的血液 mRNA 生物标志物是医学领域的一个令人兴奋的领域;营养方面的 mRNA 生物标志物具有与这些机会相平行的潜在应用。评估硒(Se)状态和需求是组织 mRNA 水平成功应用的一个领域。在大鼠肝脏 Se 缺乏时,硒蛋白-H 和硒蛋白-W 以及谷胱甘肽过氧化物酶-1(Gpx1)mRNA 高度下调,基于这些生物标志物,最低膳食 Se 需求为 0.06-0.07 μg Se/g,与使用传统生物标志物确定的需求相似。血液 Gpx1 mRNA 也可用于确定大鼠的 Se 需求,表明血液 mRNA 具有评估营养状况的潜力。需要进一步研究以开发用于所有营养素的 mRNA 生物标志物谱,以区分缺乏、边缘、充足和超营养个体和人群,并区分受益于营养补充和受营养补充不利影响的个体。