THREAD PROTEIN EXPRESSION IN NEUROECTO-DERMAL TUMOR CELL LINES OF CENTRAL NERVOUS SYSTEM ORIGIN

1993 ◽  
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pp. 291 ◽  
Author(s):  
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Jack R. Wands ◽  
Suzanne de la Monte
1991 ◽  
Vol 181 (1) ◽  
pp. 151-158 ◽  
Author(s):  
Kei Tashiro ◽  
Toru Nakano ◽  
Tasuku Honjo ◽  
Tomokazu Aoki ◽  
Shin-ichi Miyatake ◽  
...  

2021 ◽  
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Author(s):  
Bryan Ôrtero Perez Gonçalves ◽  
Gabryella Soares Pinheiro dos Santos ◽  
Warne Pedro de Andrade ◽  
Sílvia Ligório Fialho ◽  
Dawidson Assis Gomes ◽  
...  

1994 ◽  
Vol 19 (1) ◽  
pp. 25-35 ◽  
Author(s):  
Thomas Coyle ◽  
Sharon Levante ◽  
Michele Shetler ◽  
Jeffrey Winfield

1989 ◽  
Vol 11 (6) ◽  
pp. 557-561 ◽  
Author(s):  
M. Stark ◽  
T. Bilzer ◽  
N. Inoue ◽  
W. Wechsler

2017 ◽  
Vol 16 (3) ◽  
pp. 1121-1132 ◽  
Author(s):  
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Guoan Zhang ◽  
Kevin Lawlor ◽  
Arpi Nazarian ◽  
John Philip ◽  
...  

1983 ◽  
Vol 50 (03) ◽  
pp. 726-730 ◽  
Author(s):  
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Virginia McGarvey ◽  
Kim Leitzel

SummaryThis paper reports studies on the interaction between human platelets, the plasma coagulation system, and two human tumor cell lines grown in tissue culture: Melanoma and breast adenocarcinoma. The interaction was monitored through the use of 125I- labelled fibrinogen, which measures both thrombin activity generated by cell-plasma interaction and fibrin/fibrinogen binding to platelets and tumor cells. Each tumor cell line activates both the platelets and the coagulation system simultaneously resulting in the generation of thrombin or thrombin-like activity. The melanoma cells activate the coagulation system through “the extrinsic pathway” with a tissue factor-like effect on factor VII, but the breast tumor seems to activate factor X directly. Both tumor cell lines activate platelets to “make available” a platelet- derived procoagulant material necessary for the conversion of prothrombin to thrombin. The tumor-derived procoagulant activity and the platelet aggregating potential of cells do not seem to be inter-related, and they are not specific to malignant cells.


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