scholarly journals The motivations and methodology for high-throughput PET imaging of small animals in cancer research

2012 ◽  
Vol 39 (9) ◽  
pp. 1497-1509 ◽  
Author(s):  
Nicolas Aide ◽  
Eric P. Visser ◽  
Stéphanie Lheureux ◽  
Natacha Heutte ◽  
Istvan Szanda ◽  
...  
2010 ◽  
Vol 31 (10) ◽  
pp. 851-858 ◽  
Author(s):  
Nicolas Aide ◽  
Cédric Desmonts ◽  
Mélanie Briand ◽  
Mathieu Meryet-Figuiere ◽  
Laurent Poulain

2020 ◽  
Vol 67 (8) ◽  
pp. 2359-2369 ◽  
Author(s):  
S. Abdollah Mirbozorgi ◽  
Yaoyao Jia ◽  
Pengcheng Zhang ◽  
Maysam Ghovanloo

2019 ◽  
Vol 3 (1) ◽  
pp. 223-234 ◽  
Author(s):  
Hans Clevers ◽  
David A. Tuveson

Organoid cultures have emerged as powerful model systems accelerating discoveries in cellular and cancer biology. These three-dimensional cultures are amenable to diverse techniques, including high-throughput genome and transcriptome sequencing, as well as genetic and biochemical perturbation, making these models well suited to answer a variety of questions. Recently, organoids have been generated from diverse human cancers, including breast, colon, pancreas, prostate, bladder, and liver cancers, and studies involving these models are expanding our knowledge of the etiology and characteristics of these malignancies. Co-cultures of cancer organoids with non-neoplastic stromal cells enable investigation of the tumor microenvironment. In addition, recent studies have established that organoids have a place in personalized medicine approaches. Here, we describe the application of organoid technology to cancer discovery and treatment.


2010 ◽  
Author(s):  
Xin Wang ◽  
Bin Zhang ◽  
Shuangquan Liu ◽  
Xin Liu ◽  
Baoci Shan ◽  
...  

2017 ◽  
Vol 20 (3) ◽  
pp. 457-464 ◽  
Author(s):  
Daniel Gündel ◽  
Ulrike Pohle ◽  
Erik Prell ◽  
Andreas Odparlik ◽  
Oliver Thews

2010 ◽  
Vol 391 (7) ◽  
Author(s):  
Qun Bi ◽  
Taochao Tan ◽  
Xi Xiang ◽  
Aiping Lu ◽  
Shenggeng Zhu

AbstractHigh-throughput molecular profiling techniques are helpful in the diagnosis of multifactorial disease. In this study, a cDNA-phage-displayed protein microarray using phage particles spotted directly onto it as sensors was used to detect related antigens in breast tumor sera. cDNA sequences from 17 positive clones were determined, which included some sequences encoding known breast cancer-related antigens and proteins related to other diseases, as well as proteins with unknown functions. Our results not only provide some useful information for breast cancer research, but also suggest that the strategy used here would be efficient to search for disease-related proteins and other functional target proteins.


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