In HepG2 human hepatoma cells, long R3IGF-I potently suppressed the increase in IGFBP-1 protein levels induced by cAMP and theophylline.
In plain wordsIn human liver cancer cells, the long R3 IGF-I analogue strongly reduced the rise in IGFBP-1 protein caused by cAMP and theophylline.
- Peptide
- IGF-1 LR3
- Outcome
- DecreasecAMP and theophylline-induced IGFBP-1 protein levels
- Study
humann: not reported in source
HepG2 human hepatoma cells- Outcome group
- Receptor activity and mechanism · Liver
- Studied dose
- Dose not stated
Source sentences
IGF-I, IGF-II, and IGF-analogs with low IGFBP-1 affinity, (des 1-3)IGF-I and long R3IGF-I, all potently suppressed the previously characterized increase in IGFBP-1 protein levels and promoter activity induced by cAMP and theophylline.
1 context sentence(design, population, supporting numbers)
The regulation of insulin-like growth factor binding protein-1 (IGFBP-1) by its ligands, IGF-I and IGF-II, was studied in continuous cultures of HepG2 human hepatoma cells.