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微井网:高通量 3D 前列腺癌球体和药物测试平台。

The Microwell-mesh: A high-throughput 3D prostate cancer spheroid and drug-testing platform.

机构信息

Stem Cell Therapies Laboratory, Queensland University of Technology (QUT), Translational Research Institute (TRI), Brisbane, Australia.

Biochemistry division, Chemistry Department, Faculty of Science, Damietta University, Damietta, Egypt.

出版信息

Sci Rep. 2018 Jan 10;8(1):253. doi: 10.1038/s41598-017-18050-1.

DOI:10.1038/s41598-017-18050-1
PMID:29321576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5762676/
Abstract

Treatment following early diagnosis of Prostate cancer (PCa) is increasingly successful, whilst the treatment of advanced and metastatic PCa remains challenging. A major limitation in the development of new therapies is the prediction of drug efficacy using in vitro models. Classic in vitro 2-dimensional (2D) cell monolayer cultures are hypersensitive to anti-cancer drugs. As a result, there has been a surge in the development of platforms that enable three dimensional (3D) cultures thought to better replicate natural physiology and better predict drug efficacy. A deficiency associated with most 3D culture systems is that their complexity reduces the number of replicates and combination therapies that can be feasibly evaluated. Herein, we describe the use of a microwell platform that utilises a nylon mesh to retain 3D micro-tumours in discrete microwells; termed the Microwell-mesh. The Microwell-mesh enables the manufacture of ~150 micro-tumours per well in a 48-well plate, and response to anti-tumour drugs can be readily quantified. Our results demonstrate that 3D micro-tumours, unlike 2D monolayers, are not hypersensitive to Docetaxel or Abiraterone Acetate, providing a superior platform for the evaluation of sequential drug treatment. In summary, the Microwell-mesh provides an efficient 3D micro-tumour platform for single and sequential drug screening.

摘要

早期诊断前列腺癌 (PCa) 后的治疗越来越成功,而晚期和转移性 PCa 的治疗仍然具有挑战性。开发新疗法的主要限制是使用体外模型预测药物疗效。经典的体外 2 维 (2D) 细胞单层培养对抗癌药物高度敏感。因此,已经涌现出许多能够实现 3 维 (3D) 培养的平台,这些平台被认为可以更好地复制自然生理学并更好地预测药物疗效。大多数 3D 培养系统的一个缺陷是,其复杂性降低了可实际评估的重复次数和联合治疗次数。在此,我们描述了使用微井平台的情况,该平台利用尼龙网将 3D 微肿瘤保留在离散的微井中;称为微井网。微井网可在 48 孔板中每孔制造约 150 个微肿瘤,并且可以轻松定量评估抗肿瘤药物的反应。我们的结果表明,3D 微肿瘤与 2D 单层不同,对多西他赛或醋酸阿比特龙不敏感,为评估序贯药物治疗提供了优越的平台。总之,微井网为单药和序贯药物筛选提供了高效的 3D 微肿瘤平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/98944eedddad/41598_2017_18050_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/c1e432640f31/41598_2017_18050_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/764752c5d255/41598_2017_18050_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/4b6fd42fbedf/41598_2017_18050_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/fcc7b3c37802/41598_2017_18050_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/c141107dbc25/41598_2017_18050_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/ca00fee1509e/41598_2017_18050_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/98944eedddad/41598_2017_18050_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/c1e432640f31/41598_2017_18050_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/764752c5d255/41598_2017_18050_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/4b6fd42fbedf/41598_2017_18050_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/fcc7b3c37802/41598_2017_18050_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/c141107dbc25/41598_2017_18050_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/ca00fee1509e/41598_2017_18050_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d25/5762676/98944eedddad/41598_2017_18050_Fig7_HTML.jpg

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