065 A new model of in vivo tumor angiogenesis established by mixed culture of human tumor cells and murine microvascular endothelial cell line, F-2

1997 ◽  
Vol 15 (2) ◽  
pp. 113
Author(s):  
K-I. Toda ◽  
N. Kimura ◽  
R. Kannagi ◽  
S. Imamura
2010 ◽  
Vol 8 (3) ◽  
pp. 373-384 ◽  
Author(s):  
Jessica J. Huck ◽  
Mengkun Zhang ◽  
Alice McDonald ◽  
Doug Bowman ◽  
Kara M. Hoar ◽  
...  

2008 ◽  
Vol 99 (4) ◽  
pp. 810-815 ◽  
Author(s):  
Dong Yu ◽  
Emiko Sekine ◽  
Akira Fujimori ◽  
Takahiro Ochiya ◽  
Ryuichi Okayasu

2004 ◽  
Vol 2 (8) ◽  
pp. 156
Author(s):  
D. Demarquay ◽  
M. Huchet ◽  
H. Coulomb ◽  
L. Lesueur-Ginot ◽  
O. Lavergne ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Yan-Ru Chen ◽  
Wan-Ying Feng ◽  
Yuan-Xiong Cheng ◽  
Hao Zhu ◽  
Hong-Juan Liu ◽  
...  

Species-specific lncRNAs significantly determine species-specific functions through various ways, such as epigenetic regulation. However, there has been no study focusing on the role of species-specific lncRNAs in other species yet. Here, we found that siRNAs targeting mouse-specific lncRNA AA388235 could significantly induce death of human tumor cells, although it has no effect on mouse tumor cells and normal human cells. The mechanism studies showed that these siRNAs could activate the response of human tumor cells to exogenous nucleic acids, induce pyroptosis and apoptosis in the presence of GSDME, but induce apoptosis in the absence of GSDME. They also significantly inhibited the growth of human tumor cells in vivo. 17 siRNAs were designed for seven more mouse-specific lncRNAs selected randomly, among which 12 siRNAs targeting five lncRNAs induced death in human tumor cell. Our study not only demonstrates that the siRNAs designed for knocking down mouse-specific lncRNA AA388235 can be potential tumor therapeutic drugs, but also suggests that non-human species-specific lncRNAs are a huge potential library that can be used to design siRNAs for tumor treatment. Large-scale screening based on this is promising.


2015 ◽  
Vol 14 (2) ◽  
pp. 99-104 ◽  
Author(s):  
N. V. Golubtsova ◽  
O. S. Burova ◽  
K. A. Baryshnikov ◽  
M. V. Oborotova ◽  
V. I. Karaseva ◽  
...  

MAb against the antigen CD117 - stem marker of human tumor cells. Strain 406 PPI prepared by cell fusion of mouse myeloma NS-1 cells with spleen mice BALB/ C, pre-immunized three times at an interval of two weeks, the cells of the cell line of human melanoma melKor. Merging conducted using a solution of PEG/DMSO. For screening received mAb 406 used human melanoma cell lines which differed in the expression of CD117 antigen FSBSI "N.N. Blokhin RCRC" collection. N.N Blokhin. Antigen expression was studied in immunofluorescence and evaluated on a flow cytometer BD FACS CantoTMII. ICA IC0-406 was compared with commercial ICA against antigen CD 117 (Germany). The results indicated the identity of the frequency of antigen-positive cases and the percentage of antigen cells. ICA IC0-406 block binding to cells melKor ICA anti-CD117. Linking ICA IC0-406 antigen-positive cells causes modulation of antigen CD 117.


2005 ◽  
Vol 46 (3) ◽  
pp. 363-372 ◽  
Author(s):  
Tomoaki YAHIRO ◽  
Shigeki MASUI ◽  
Nobuo KUBOTA ◽  
Koji YAMADA ◽  
Ataru KOBAYASHI ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document