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Hematol Oncol ; 12(2): 53-60, 1994.
Article in English | MEDLINE | ID: mdl-8070754

ABSTRACT

In order to clarify the function of P210 bcr/abl oncogene in leukemogenesis, IL-3 dependent murine hematopietic cell line, FDC-P2, was transfected with the plasmid containing cDNA of P210 bcr/abl oncogene (pGD'210) or murine IL-3 (pcDmIL3) by electroporation. Four out of five pGDH210 transfected clones as well as FDC-P2 transfected with pcDmIL3, acquired autonomous proliferation (i.e. lost the requirement for IL-3 supplementation). The expression of bcr/abl oncogene was weak in one clone, which remained dependent on IL-3. Unlike pcDmIL3 transfectants, which secrete IL-3 into the supernatant, IL-3 was not demonstrated in the culture supernatant of pGD'210 transfected FDC-P2. These finding suggest that P210 bcr/abl oncogene is directly associated with autonomous proliferation, which is the first process of leukemogenesis.


Subject(s)
Cell Division , Fusion Proteins, bcr-abl/biosynthesis , Genes, abl , Oncogenes , Transfection , Animals , Base Sequence , Cell Line , Culture Media, Conditioned , DNA Primers , Electroporation/methods , Hematopoietic Stem Cells , Interleukin-3/biosynthesis , Mice , Molecular Sequence Data , Plasmids , Polymerase Chain Reaction
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