通过激光烧蚀-ICP-质谱法定量测定单个乳腺肿瘤细胞中的铂类药物并绘制其亚细胞图谱

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-31 DOI:10.1039/d4dt02467b
Legna Colina Vegas, Thibaut Van Acker, Wilmer Villarreal, Olivier De Wever, Alzir A Batista, Joaquim A. Nobrega, Frank Vanhaecke
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引用次数: 0

摘要

多年来,癌症已成为全球第二大死因,仅次于心血管疾病。专注于发现治疗癌症新药的研究小组越来越多,其目的是寻找更有效的化合物,这些化合物的副作用较小,而且不会产生耐药性。顺铂和卡铂金属复合物被广泛用于各种癌症的化疗,包括三阴性乳腺癌(TNBC)。这两种化合物在现代化疗中至关重要,并一直是优化其治疗特性和减少不良反应的研究课题。激光烧蚀-电感耦合等离子体质谱法(LA-ICP-MS)可以获得生物组织和单细胞群中元素的定量数据和空间分布信息。本研究通过 LA-ICP-MS 分析测定了 TNBC MDA-MB-231 细胞在与不同含铂药物培养后的铂含量及其分布情况。单细胞定量分析和元素图谱揭示了铂在细胞内外的分布,有助于深入了解这些含铂药物的潜在作用机制及其对 TNBC 的疗效。
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Quantitative determination and subcellular mapping of Pt-based drugs in single breast tumour cells via Laser Ablation – ICP-Mass Spectrometry
For years already, cancer is the second cause of death worldwide, preceded by cardiovascular diseases only. The number of research groups focusing on the discovery of new drugs to treat cancer is growing and the aim is to look for more effective compounds that cause less severe side effects and do not suffer from therapeutic resistance. The metal complexes Cisplatin and Carboplatin are widely used in the chemotherapeutic treatment of various types of cancer, including triple-negative breast cancer (TNBC). Both compounds are essential in modern chemotherapy and continue to be the subject of research to optimize their therapeutic properties and minimize adverse effects. Laser ablation – inductively coupled plasma-mass spectrometry (LA-ICP-MS) allows both quantitative data and information on the spatial distribution of elements in biological tissues and populations of single cells to be obtained. In this work, the content of Pt and its distribution in TNBC MDA-MB-231 cells were determined via LA-ICP-MS analysis after incubation with different Pt-containing drugs. The quantitative analysis of single cells and the elemental maps revealing the distribution of Pt over and within the cells provide an enhanced insight into the potential mechanism of action of these Pt-containing drugs and their efficacy against TNBC.
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7.20
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4.30%
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567
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