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Characterization of drug effects on cell cultures from phase-contrast microscopy images
D. Baručić, S. Kaushik, J. Kybic, J. Stanková, P. Džubák, M. Hajdúch
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 2003-01-01 do 2023-12-31
Nursing & Allied Health Database (ProQuest)
od 2003-01-01 do 2023-12-31
Health & Medicine (ProQuest)
od 2003-01-01 do 2023-12-31
- MeSH
- buněčné kultury * MeSH
- mikroskopie fázově kontrastní MeSH
- neuronové sítě * MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
In this work, we classify chemotherapeutic agents (topoisomerase inhibitors) based on their effect on U-2 OS cells. We use phase-contrast microscopy images, which are faster and easier to obtain than fluorescence images and support live cell imaging. We use a convolutional neural network (CNN) trained end-to-end directly on the input images without requiring for manual segmentations or any other auxiliary data. Our method can distinguish between tested cytotoxic drugs with an accuracy of 98%, provided that their mechanism of action differs, outperforming previous work. The results are even better when substance-specific concentrations are used. We show the benefit of sharing the extracted features over all classes (drugs). Finally, a 2D visualization of these features reveals clusters, which correspond well to known class labels, suggesting the possible use of our methodology for drug discovery application in analyzing new, unseen drugs.
Citace poskytuje Crossref.org
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- $a Baručić, Denis $u Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czech Republic. Electronic address: barucden@fel.cvut.cz
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- $a In this work, we classify chemotherapeutic agents (topoisomerase inhibitors) based on their effect on U-2 OS cells. We use phase-contrast microscopy images, which are faster and easier to obtain than fluorescence images and support live cell imaging. We use a convolutional neural network (CNN) trained end-to-end directly on the input images without requiring for manual segmentations or any other auxiliary data. Our method can distinguish between tested cytotoxic drugs with an accuracy of 98%, provided that their mechanism of action differs, outperforming previous work. The results are even better when substance-specific concentrations are used. We show the benefit of sharing the extracted features over all classes (drugs). Finally, a 2D visualization of these features reveals clusters, which correspond well to known class labels, suggesting the possible use of our methodology for drug discovery application in analyzing new, unseen drugs.
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- $a Kaushik, Sumit $u Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czech Republic. Electronic address: kaushsum@fel.cvut.cz
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- $a Kybic, Jan $u Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czech Republic. Electronic address: kybic@fel.cvut.cz
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- $a Stanková, Jarmila $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic
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- $a Džubák, Petr $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic
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- $a Hajdúch, Marián $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic
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