Publication | Open Access
Induction of tumor promotor-inducible genes in murine 3T3 cell lines and tetradecanoyl phorbol acetate-nonproliferative 3T3 variants can occur through protein kinase C-dependent and -independent pathways.
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Citations
30
References
1989
Year
Murine 3T3Epidermal Growth FactorTumor Promotor-inducible GenesImmunologyCell ProliferationCancer BiologyCellular PhysiologyTumor BiologySignaling PathwayTpa PretreatmentReceptor Tyrosine KinaseFibroblast Growth FactorRadiation OncologyCell SignalingCancer ResearchHealth SciencesOncogenic AgentCell LinesCancer GeneticsCell BiologyTumor MicroenvironmentSignal TransductionTis GenesTumor SuppressorMedicine
We isolated a group of genes that are rapidly and transiently induced in 3T3 cells by tetradecanoyl phorbol acetate (TPA). These genes are called TIS genes (for TPA-inducible sequences). Epidermal growth factor (EGF), fibroblast growth factor (FGF), and TPA activated TIS gene expression with similar induction kinetics. TPA pretreatment to deplete protein kinase C activity did not abolish the subsequent induction of TIS gene expression by epidermal growth factor or fibroblast growth factor; both peptide mitogens can activate TIS genes through a protein kinase C-independent pathway(s). We also analyzed TIS gene expression in three TPA-nonproliferative variants (3T3-TNR2, 3T3-TNR9, and A31T6E12A). The results indicate that (i) modulation of a TPA-responsive sodium-potassium-chloride transport system is not necessary for TIS gene induction either by TPA or by other mitogens and (ii) TIS gene induction is not sufficient to guarantee a proliferative response to mitogenic stimulation.
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