Bioengineering & Translational Medicine
Autor: | Shelly R. Peyton, Hyuna Kim, Sualyneth Galarza, Naciye Atay, Jennifer M. Munson |
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Přispěvatelé: | Biomedical Engineering and Mechanics |
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
cell migration
effect size lcsh:Biotechnology Biomedical Engineering Pharmaceutical Science Motility Biology 03 medical and health sciences 0302 clinical medicine breast cancer In vivo lcsh:TP248.13-248.65 medicine metastasis lcsh:Chemical engineering 030304 developmental biology Cell invasion 0303 health sciences lcsh:RM1-950 glioblastoma lcsh:TP155-156 Cell migration medicine.disease invasion In vitro 3. Good health Cell biology lcsh:Therapeutics. Pharmacology 030220 oncology & carcinogenesis Cellular motility Wound healing Biotechnology Glioblastoma |
Zdroj: | Bioengineering & Translational Medicine, Vol 5, Iss 1, Pp n/a-n/a (2020) |
ISSN: | 2380-6761 |
Popis: | Cell motility is a critical aspect of several processes, such as wound healing and immunity; however, it is dysregulated in cancer. Current limitations of imaging tools make it difficult to study cell migration in vivo. To overcome this, and to identify drivers from the microenvironment that regulate cell migration, bioengineers have developed 2D (two-dimensional) and 3D (three-dimensional) tissue model systems in which to study cell motility in vitro, with the aim of mimicking elements of the environments in which cells move in vivo. However, there has been no systematic study to explicitly relate and compare cell motility measurements between these geometries or systems. Here, we provide such analysis on our own data, as well as across data in existing literature to understand whether, and which, metrics are conserved across systems. To our surprise, only one metric of cell movement on 2D surfaces significantly and positively correlates with cell migration in 3D environments (percent migrating cells), and cell invasion in 3D has a weak, negative correlation with glioblastoma invasion in vivo. Finally, to compare across complex model systems, in vivo data, and data from different labs, we suggest that groups report an effect size, a statistical tool that is most translatable across experiments and labs, when conducting experiments that affect cellular motility. National Cancer InstituteUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Cancer Institute (NCI) [R21CA223783, R37CA22563]; National Institute of General Medical SciencesUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of General Medical Sciences (NIGMS) [T32GM135096]; National Science FoundationNational Science Foundation (NSF) [DMR-1454806] National Cancer Institute, Grant/Award Numbers: R21CA223783, R37CA22563; National Institute of General Medical Sciences, Grant/Award Number: T32GM135096; National Science Foundation, Grant/Award Number: DMR-1454806 |
Databáze: | OpenAIRE |
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