Spectropolarimetric comparison of molecular-genetic study of BRCA1 gene mutation types in patients with breast cancer and their relatives

O. Peresunko, Tatjana V. Kruk, Kateryna M. Chala, S. Yermolenko, Denis G. Gostyuk, I. Gruia
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Abstract

This work is devoted to the substantiation and selection of patients with breast cancer (BC) for the purpose of conducting expensive molecular genetic studies on genotyping. As diagnostic methods have been used ultraviolet spectrometry samples of blood plasma in the liquid state, infrared spectroscopy middle range (2,5 - 25 microns) dry residue of plasma polarization and laser diagnostic technique of thin histological sections of biological tissues. Obtained results showed that the use of spectrophotometry in the range of 1000-3000 cm-1 allowed to establish quantitative parameters of the plasma absorption rate of blood of patients in the third group in different ranges, which would allow in the future to conduct an express analysis of the patient's condition (procedure screening) for further molecular-genetic typing on BRCA I and II.
乳腺癌患者及其亲属BRCA1基因突变类型分子遗传学研究的光谱偏振比较
这项工作致力于证实和选择乳腺癌(BC)患者,以进行昂贵的基因分型分子遗传学研究。作为诊断方法,目前已采用紫外光谱法对液态血浆样品进行检测,红外光谱法对中范围(2,5 - 25微米)干残等离子体偏振和激光对生物组织薄切片进行诊断等技术。所得结果表明,在1000-3000 cm-1范围内使用分光光度法可以建立第三组患者不同范围内血液血浆吸收率的定量参数,为将来对患者的病情进行快速分析(程序筛选),进一步进行BRCA I和II的分子遗传学分型提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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