scholarly journals 3D High‐Content Culturing and Drug Screening Platform to Study Vascularized Hepatocellular Carcinoma in Hypoxic Condition

2021 ◽  
pp. 2100078
Author(s):  
Jungeun Lim ◽  
Hyeri Choi ◽  
Jungho Ahn ◽  
Noo Li Jeon

2018 ◽  
Vol 425 ◽  
pp. 54-64 ◽  
Author(s):  
Haisen Yin ◽  
Risheng Que ◽  
Chunying Liu ◽  
Weidan Ji ◽  
Bin Sun ◽  
...  


2009 ◽  
Vol 15 (13) ◽  
pp. 4322-4335 ◽  
Author(s):  
Chee-Wai Chua ◽  
Yung-Tuen Chiu ◽  
Hiu-Fung Yuen ◽  
Kwok-Wah Chan ◽  
Kwan Man ◽  
...  


2020 ◽  
Author(s):  
Alexandra Lubin ◽  
Jason Otterstrom ◽  
Yvette Hoade ◽  
Ivana Bjedov ◽  
Eleanor Stead ◽  
...  

AbstractZebrafish provide a unique opportunity for drug screening in living animals, with the fast developing, transparent embryos allowing for relatively high throughput, microscopy-based screens. However, the limited availability of rapid, flexible imaging and analysis platforms has limited the use of zebrafish in drug screens. We have developed a easy-to-use, customisable automated screening procedure suitable for high-throughput phenotype-based screens of live zebrafish. We utilised the WiScan®Hermes High Content Imaging System to rapidly acquire brightfield and fluorescent images of embryos, and the WiSoft®Athena Zebrafish Application for analysis, which harnesses an Artificial Intelligence-driven algorithm to automatically detect fish in brightfield images, identify anatomical structures, partition the animal into regions, and exclusively select the desired side-oriented fish. Our initial validation combined structural analysis with fluorescence images to enumerate GFP-tagged haematopoietic stem and progenitor cells in the tails of embryos, which correlated with manual counts. We further validated this system to assess the effects of genetic mutations and x-ray irradiation in high content using a wide range of assays. Further, we performed simultaneous analysis of multiple cell types using dual fluorophores in high throughput. In summary, we demonstrate a broadly applicable and rapidly customisable platform for high content screening in zebrafish.



2014 ◽  
Vol 59 (2) ◽  
pp. 753-762 ◽  
Author(s):  
Anita Ordas ◽  
Robert-Jan Raterink ◽  
Fraser Cunningham ◽  
Hans J. Jansen ◽  
Malgorzata I. Wiweger ◽  
...  

ABSTRACTThe translational value of zebrafish high-throughput screens can be improved when more knowledge is available on uptake characteristics of potential drugs. We investigated reference antibiotics and 15 preclinical compounds in a translational zebrafish-rodent screening system for tuberculosis. As a major advance, we have developed a new tool for testing drug uptake in the zebrafish model. This is important, because despite the many applications of assessing drug efficacy in zebrafish research, the current methods for measuring uptake using mass spectrometry do not take into account the possible adherence of drugs to the larval surface. Our approach combines nanoliter sampling from the yolk using a microneedle, followed by mass spectrometric analysis. To date, no single physicochemical property has been identified to accurately predict compound uptake; our method offers a great possibility to monitor how any novel compound behaves within the system. We have correlated the uptake data with high-throughput drug-screening data fromMycobacterium marinum-infected zebrafish larvae. As a result, we present an improved zebrafish larva drug-screening platform which offers new insights into drug efficacy and identifies potential false negatives and drugs that are effective in zebrafish and rodents. We demonstrate that this improved zebrafish drug-screening platform can complement conventional models ofin vivoMycobacterium tuberculosis-infected rodent assays. The detailed comparison of two vertebrate systems, fish and rodent, may give more predictive value for efficacy of drugs in humans.



BMC Cancer ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Andrew Riley ◽  
Victoria Green ◽  
Ramsah Cheah ◽  
Gordon McKenzie ◽  
Laszlo Karsai ◽  
...  


2015 ◽  
Author(s):  
Rajni Kant ◽  
Lucas Tung ◽  
Chung-Kuang Lu ◽  
Yi-Ming Chen ◽  
Chia-Hung Yen


Author(s):  
Hallie A. Swan ◽  
Rachele Rosati ◽  
Caroline Bridgwater ◽  
Michael J. Churchill ◽  
Roland M. Watt ◽  
...  


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