TRANSFORMING GROWTH FACTOR beta2 UPREG-ULATES GM-CSF GENE IN HUMAN BLADDER CARCINOMA CELL LINE HTB 5637

2000 ◽  
Vol 28 (5) ◽  
pp. A341-A341
Author(s):  
B. Goliaei ◽  
Z. Soheili
Blood ◽  
1985 ◽  
Vol 66 (3) ◽  
pp. 748-751
Author(s):  
T Hoang ◽  
EA McCulloch

Circulating blast cells from the peripheral blood of acute myeloblastic leukemia patients include a subpopulation capable of colony formation in the presence of phytohemagglutinin-stimulated leukocyte-conditioned medium (PHA-LCM). We describe the complete replacement in the blast assay of PHA-LCM by conditioned medium from a human bladder carcinoma cell line, HTB9. Both conditioned media contain a stimulator of blast cell growth that elutes as a single peak from a Sephadex G100 column with an apparent molecular weight of 30,000. It is shown that this leukemic blast growth factor is distinct from erythroid-potentiating activity (EPA) and possibly granulocyte macrophage colony-stimulating factor.


Blood ◽  
1985 ◽  
Vol 66 (3) ◽  
pp. 748-751 ◽  
Author(s):  
T Hoang ◽  
EA McCulloch

Abstract Circulating blast cells from the peripheral blood of acute myeloblastic leukemia patients include a subpopulation capable of colony formation in the presence of phytohemagglutinin-stimulated leukocyte-conditioned medium (PHA-LCM). We describe the complete replacement in the blast assay of PHA-LCM by conditioned medium from a human bladder carcinoma cell line, HTB9. Both conditioned media contain a stimulator of blast cell growth that elutes as a single peak from a Sephadex G100 column with an apparent molecular weight of 30,000. It is shown that this leukemic blast growth factor is distinct from erythroid-potentiating activity (EPA) and possibly granulocyte macrophage colony-stimulating factor.


1987 ◽  
Vol 8 (5) ◽  
pp. 301-305 ◽  
Author(s):  
FUSAYUKI OMORI ◽  
SEIICHI OKAMURA ◽  
SHIN HAYASHI ◽  
SHIGERU YAMAGA ◽  
TSUNEFUMI SHIBUYA ◽  
...  

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