scholarly journals Ortho-coumaric acid derivatives with therapeutic potential in a three-dimensional culture of the immortalised U-138 MG glioblastoma multiforme cell line

Author(s):  
Yanet Karina Gutiérrez Mercado ◽  
Juan Carlos Mateos Díaz ◽  
Doddy Denise Ojeda Hernández ◽  
Francisco Javier López Gonzalez ◽  
Edwin Estefan Reza Zaldivar ◽  
...  
1996 ◽  
Vol 12 (4-6) ◽  
pp. 389-389
Author(s):  
P. Penfornis ◽  
B. Benoit ◽  
S. Thenet-Gauci ◽  
O. Houcine ◽  
F. Marano ◽  
...  

2017 ◽  
Vol 69 (6) ◽  
pp. 925-931 ◽  
Author(s):  
Jane Marie Tonello ◽  
Saori Kawashima ◽  
Kazuki Sato ◽  
Yoshinori Kawabe ◽  
Akira Ito ◽  
...  

2014 ◽  
Vol 45 (5) ◽  
pp. 2108-2116 ◽  
Author(s):  
PHANTHAKARN TIT-OON ◽  
DARANEE CHOKCHAICHAMNANKIT ◽  
AMNART KHONGMANEE ◽  
PHANEE SAWANGAREETRAKUL ◽  
JISNUSON SVASTI ◽  
...  

2017 ◽  
Vol 68 (6) ◽  
pp. 1341-1344
Author(s):  
Grigore Berea ◽  
Gheorghe Gh. Balan ◽  
Vasile Sandru ◽  
Paul Dan Sirbu

Complex interactions between stem cells, vascular cells and fibroblasts represent the substrate of building microenvironment-embedded 3D structures that can be grafted or added to bone substitute scaffolds in tissue engineering or clinical bone repair. Human Adipose-derived Stem Cells (hASCs), human umbilical vein endothelial cells (HUVECs) and normal dermal human fibroblasts (NDHF) can be mixed together in three dimensional scaffold free constructs and their behaviour will emphasize their potential use as seeding points in bone tissue engineering. Various combinations of the aforementioned cell lines were compared to single cell line culture in terms of size, viability and cell proliferation. At 5 weeks, viability dropped for single cell line spheroids while addition of NDHF to hASC maintained the viability at the same level at 5 weeks Fibroblasts addition to the 3D construct of stem cells and endothelial cells improves viability and reduces proliferation as a marker of cell differentiation toward osteogenic line.


2020 ◽  
Vol 27 ◽  
Author(s):  
Ji-Yeon Lee ◽  
Myoung Hee Kim

: HOX genes belong to the highly conserved homeobox superfamily, responsible for the regulation of various cellular processes that control cell homeostasis, from embryogenesis to carcinogenesis. The abnormal expression of HOX genes is observed in various cancers, including breast cancer; they act as oncogenes or as suppressors of cancer, according to context. In this review, we analyze HOX gene expression patterns in breast cancer and examine their relationship, based on the three-dimensional genome structure of the HOX locus. The presence of non-coding RNAs, embedded within the HOX cluster, and the role of these molecules in breast cancer have been reviewed. We further evaluate the characteristic activity of HOX protein in breast cancer and its therapeutic potential.


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