Tumor biomarkers for diagnosis, prognosis and targeted therapy

生物标志物发现 生物标志物 精密医学 医学 个性化医疗 癌症 分子生物标志物 癌症生物标志物 癌变 生物信息学 计算生物学 肿瘤科 内科学 病理 生物 蛋白质组学 生物化学 基因
作者
Yue Zhou,Lei Tao,Jiahao Qiu,Jing Xu,Xinyu Yang,Yu Zhang,Xinyu Tian,Xinqi Guan,Xiaobo Cen,Yinglan Zhao
出处
期刊:Signal Transduction and Targeted Therapy [Springer Nature]
卷期号:9 (1) 被引量:80
标识
DOI:10.1038/s41392-024-01823-2
摘要

Abstract Tumor biomarkers, the substances which are produced by tumors or the body’s responses to tumors during tumorigenesis and progression, have been demonstrated to possess critical and encouraging value in screening and early diagnosis, prognosis prediction, recurrence detection, and therapeutic efficacy monitoring of cancers. Over the past decades, continuous progress has been made in exploring and discovering novel, sensitive, specific, and accurate tumor biomarkers, which has significantly promoted personalized medicine and improved the outcomes of cancer patients, especially advances in molecular biology technologies developed for the detection of tumor biomarkers. Herein, we summarize the discovery and development of tumor biomarkers, including the history of tumor biomarkers, the conventional and innovative technologies used for biomarker discovery and detection, the classification of tumor biomarkers based on tissue origins, and the application of tumor biomarkers in clinical cancer management. In particular, we highlight the recent advancements in biomarker-based anticancer-targeted therapies which are emerging as breakthroughs and promising cancer therapeutic strategies. We also discuss limitations and challenges that need to be addressed and provide insights and perspectives to turn challenges into opportunities in this field. Collectively, the discovery and application of multiple tumor biomarkers emphasized in this review may provide guidance on improved precision medicine, broaden horizons in future research directions, and expedite the clinical classification of cancer patients according to their molecular biomarkers rather than organs of origin.
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