Kamel Hala Fawzy Mohamed, Al-Amodi Hiba Saeed A Bagader
Biochemistry Department, Faculty of Medicine, Umm AL-Qura University, Makhha 21955, Saudi Arabia; Medical Biochemistry Department, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt.
Biochemistry Department, Faculty of Medicine, Umm AL-Qura University, Makhha 21955, Saudi Arabia.
Genomics Proteomics Bioinformatics. 2017 Aug;15(4):220-235. doi: 10.1016/j.gpb.2016.11.005. Epub 2017 Aug 13.
Cancer therapy agents have been used extensively as cytotoxic drugs against tissue or organ of a specific type of cancer. With the better understanding of molecular mechanisms underlying carcinogenesis and cellular events during cancer progression and metastasis, it is now possible to use targeted therapy for these molecular events. Targeted therapy is able to identify cancer patients with dissimilar genetic defects at cellular level for the same cancer type and consequently requires individualized approach for treatment. Cancer therapy begins to shift steadily from the traditional approach of "one regimen for all patients" to a more individualized approach, through which each patient will be treated specifically according to their specific genetic defects. Personalized medicine accordingly requires identification of indicators or markers that guide in the decision making of such therapy to the chosen patients for more effective therapy. Cancer biomarkers are frequently used in clinical practice for diagnosis and prognosis, as well as identification of responsive patients and prediction of treatment response of cancer patient. The rapid breakthrough and development of microarray and sequencing technologies is probably the main tool for paving the way toward "individualized biomarker-driven cancer therapy" or "personalized medicine". In this review, we aim to provide an updated knowledge and overview of the current landscape of cancer biomarkers and their role in personalized medicine, emphasizing the impact of genomics on the implementation of new potential targeted therapies and development of novel cancer biomarkers in improving the outcome of cancer therapy.
癌症治疗药物已被广泛用作针对特定类型癌症的组织或器官的细胞毒性药物。随着对癌症发生以及癌症进展和转移过程中细胞事件的分子机制有了更深入的了解,现在有可能针对这些分子事件进行靶向治疗。靶向治疗能够在细胞水平上识别同一癌症类型中具有不同遗传缺陷的癌症患者,因此需要采取个体化的治疗方法。癌症治疗正开始稳步从传统的“所有患者采用一种治疗方案”方法转向更个体化的方法,通过这种方法,每个患者将根据其特定的遗传缺陷进行专门治疗。相应地,个性化医疗需要识别指标或标志物,以指导针对选定患者进行此类治疗的决策,从而实现更有效的治疗。癌症生物标志物在临床实践中经常用于诊断和预后,以及识别有反应的患者和预测癌症患者的治疗反应。微阵列和测序技术的迅速突破和发展可能是为“个体化生物标志物驱动的癌症治疗”或“个性化医疗”铺平道路的主要工具。在这篇综述中,我们旨在提供关于癌症生物标志物的当前状况及其在个性化医疗中的作用的最新知识和概述,强调基因组学对实施新的潜在靶向治疗以及开发新型癌症生物标志物以改善癌症治疗结果的影响。