适体
类有机物
免疫染色
计算生物学
细胞凋亡
细胞色素c
癌症研究
癌症
生物
化学
病理
医学
分子生物学
细胞生物学
生物化学
免疫组织化学
遗传学
作者
Tran N.H. Nguyen,Lisa F. Horowitz,Timothy Krilov,Ethan Lockhart,Heidi L. Kenerson,Taranjit S. Gujral,Raymond S. Yeung,Netzahualcóyotl Arroyo‐Currás,Albert Folch
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-09-06
卷期号:10 (36)
标识
DOI:10.1126/sciadv.adn5875
摘要
Functional assays on intact tumor biopsies can complement genomics-based approaches for precision oncology, drug testing, and organs-on-chips cancer disease models by capturing key therapeutic response determinants, such as tissue architecture, tumor heterogeneity, and the tumor microenvironment. Most of these assays rely on fluorescent labeling, a semiquantitative method best suited for single-time-point assays or labor-intensive immunostaining analysis. Here, we report integrated aptamer electrochemical sensors for on-chip, real-time monitoring of cytochrome C, a cell death indicator, from intact microdissected tissues with high affinity and specificity. The platform features a multi-well sensor layout and a multiplexed electronic setup. The aptasensors measure increases in cytochrome C in the supernatant of mouse or human microdissected tumors after exposure to various drug treatments. Because of the sensor’s high affinity, it primarily tracks rising concentrations of cytochrome C, capturing dynamic changes during apoptosis. This approach could help develop more advanced cancer disease models and apply to other complex in vitro disease models, such as organs-on-chips and organoids.
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