Biomarkers of cell death applicable to early clinical trials

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• 作者：Emma Dean¹ ; ^{edean@picr.man.ac.uk} ; Alastair Greystoke¹ ; ^{agreystoke@picr.man.ac.uk} ; Malcolm Ranson ^{malcolm.ranson@christie.nhs.uk} ; Caroline Dive ^{cdive@picr.man.ac.uk}
• 关键词：Biomarkers ; Cell death ; Apoptosis ; Predictive ; Circulating
• 刊名：Experimental Cell Research
• 出版年：2012
• 期刊代码：292_00144827
• 类别：med
• 出版时间：1 July, 2012
• 卷：318
• 期：11
• 页码：1252-1259
• 文件大小：384 K

摘要

The development of biomarkers of cell death to reflect tumor biology and drug-induced response has garnered interest with the development of several classes of drugs aimed at decreasing the cellular threshold for apoptosis and exploiting pre-existing oncogenic stresses. These novel anticancer drugs, directly targeted to the apoptosis regulatory machinery and aimed at abrogating survival signaling pathways, are entering early clinical trials provoking the question of how to monitor their impact on cancer patients. The parallel development of drugs with predictive biomarkers and their incorporation into early clinical trials are anticipated to support the pharmacological audit trail, to speed the development and reduce the attrition rate of novel drugs whose objective is to provoke tumor cell death. Tumor biopsies are an ideal matrix to measure apoptosis, but surrogate less invasive biomarkers such as blood samples and functional imaging are less challenging to acquire clinically. Archetypal and exploratory examples illustrating the importance of biomarkers to drug development are given. This review explores the substantive challenges associated with the validation, deployment, interpretation and utility of biomarkers of cell death and reviews recent advances in their incorporation in preclinical and early clinical trial contexts.