使用联合建模方法的药物发现中的生物标志物和生物活性

Kawsher Rahman
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摘要

对于加强诊断、观察药物相关活性和治疗反应,以及为各种慢性疾病开发更安全、更直接的治疗方案,需要经过验证和强大的生物标志物。当涉及到药物的发现和开发时,各种各样的生物标志物已经被证明是有影响的,但是涉及识别和验证特定疾病的生物标志物的程序已经被证明是麻烦的。近年来,转录组学、细胞组学、基因组学、蛋白质组学、代谢组学和成像等多组学方法取得了一些进展。这些进步使复杂慢性疾病的独特生物标志物的发现和开发得以迅速加快。尽管仍有许多缺陷需要研究,但正在进行的发现和改进疾病相关生物标志物的努力将大大有助于优化药物开发整个过程的决策,并扩大我们对感染过程的理解。此外,当临床前生物标志物被有效地转化为临床时,将为在复杂的疾病环境中同样有效地实施个性化治疗铺平道路,从而使患者、医疗保健服务提供者和生物制药行业受益。
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Biomarkers and Bioactivity in Drug Discovery using a Joint Modelling Approach
Biomarkers that are validated and robust are required for the enhancement of diagnosis, the observation of drug-related activity, therapeutic reactions, and as the blueprint for developing safer and more direct therapeutic efforts for a variety of chronic ailments. Various kinds of biomarkers have proven impactful when it comes to the discovery and development of drugs, but the procedure that involves identifying and verifying ailment-specific biomarkers has proven to be hassling. In recent times, there have been some advancements in multiple omics (also known as multi-omics) methods like transcriptomic, cytometry, genomics, proteomics, metabolomics and imaging. These advancements have made it possible for the discovery and development of distinct biomarkers for complicated chronic ailments to be accelerated expeditiously. In spite of the fact that numerous drawbacks still need to be looked into, ongoing efforts for the discovery and improvement of illness-associated biomarkers will go a long way in optimizing decision-making across the entire process of drug development and expand our comprehension of the infection processes. In addition, when the preclinical biomarkers are effectively translated into the clinic, the way will pave well to an equally effective implementation of personalized therapies throughout complicated illness environments to become beneficial to patients, healthcare service providers and the industry of bio-pharma.  
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