Iyer Preethi M, Karthikeyan S, Sanjay Kumar P, Krishnan Namboori P K
Department of Electronics and Communication Engineering, M.Tech-Biomedical Engineering Amrita School of Engineering, AMRITA Vishwa Vidyapeetham Amrita University, Amritanagar, Ettimadai, Coimbatore, Tamil Nadu, 641112, India.
Amrita School of Engineering, AMRITA Vishwa Vidyapeetham Amrita University, Amritanagar, Ettimadai, Coimbatore, Tamil Nadu, 641112, India.
Funct Integr Genomics. 2017 Jul;17(4):375-385. doi: 10.1007/s10142-017-0559-7. Epub 2017 May 3.
The proneness of diseases and susceptibility towards drugs vary from person to person. At present, there is a strong demand for the personalization of drugs. The genetic signature behind proneness of the disease has been studied through a comprehensive 'octopodial approach'. All the genetic variants included in the approach have been introduced. The breast cancer associated with BRCA1 mutation has been taken as the illustrative example to introduce all these factors. The genetic variants associated with the drug action of tamoxifen have been fully illustrated in the manuscript. The design of a new personalized anti-breast cancer drug has been explained in the third phase. For the design of new personalized drugs, a metabolite of anti-cancer drug chlorambucil has been taken as the template. The design of drug has been made with respect to the protein 1T15 of BRCA1 gene corresponding to the genetic signature of rs28897696.
疾病的易感性和对药物的敏感性因人而异。目前,对药物个性化有强烈需求。已通过全面的“八足方法”研究了疾病易感性背后的基因特征。该方法中包含的所有基因变异均已介绍。与BRCA1突变相关的乳腺癌已作为示例引入所有这些因素。他莫昔芬药物作用相关的基因变异在稿件中已充分说明。第三阶段解释了新型个性化抗乳腺癌药物的设计。对于新型个性化药物的设计,已将抗癌药物苯丁酸氮芥的一种代谢物作为模板。已针对与rs28897696基因特征相对应的BRCA1基因的蛋白质1T15进行了药物设计。