癌症治疗药物敏感性试验、技术分析及趋势。

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Da-Yong Lu, Ting-Ren Lu
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引用次数: 1

摘要

在过去的二十年中,世界范围内用于抗癌治疗的药物敏感性试验(DST)的技术和质量得到了迅速发展。DST的大部分进展来自技术通用性的先进系统(更快、高通量、高灵敏度和肿瘤数量更小)。DST作为最早的药物选择系统,生物医学知识和技术进步是相互支持的。更重要的是,这些技术进步解决了许多药理学争议。随着这一技术的进步,DST的临床前景进入了一个新的阶段(每次检测>500个样本,肿瘤细胞数量极低)。作为药物选择系统的先驱,DST等待着能够适应临床复杂治疗情况和多样化肿瘤类别的新版本。通过坚持这一致病和治疗多样性的目标,DST最终可以通过建立高质量的药物选择系统来治愈更多的癌症患者。为了使DST的顺利开展,需要在化疗前增加对肿瘤生物学、病理学和药理学(肿瘤异质性、可塑性、转移和耐药)的了解,并提供充分的信息参数。在本文中,特别强调了对DST的医学和技术见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug Sensitivity Testing for Cancer Therapy, Technique Analysis and Trends.

The techniques and qualities of drug sensitivity testing (DST) for anticancer treatment have grown rapidly in the past two decades worldwide. Much of DST progress came from advanced systems of technical versatility (faster, highly-throughput, highly-sensitive, and smaller in tumor quantity). As the earliest drug selective system, biomedical knowledge and technical advances for DST are mutually supported. More importantly, many pharmacological controversies are resolved by these technical advances. With this technical stride, the clinical landscape of DST entered into a new phase (>500 samples per testing and extremely low quantity of tumor cells). As a forerunner of the drug selection system, DST awaits a new version that can adapt to complicated therapeutic situations and diverse tumor categories in the clinic. By upholding this goal of pathogenic and therapeutic diversity, DST could eventually cure more cancer patients by establishing high-quality drug selection systems. To smoothen DST development, there is a need to increase the understanding of cancer biology, pathology and pharmacology (cancer heterogeneity, plasticity, metastasis and drug resistance) with well-informative parameters before chemotherapy. In this article, medicinal and technical insights into DST are especially highlighted.

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来源期刊
CiteScore
4.80
自引率
9.10%
发文量
55
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