In PC-3 prostate cancer cells, the NKX3.1 attenuation of IGF-I signaling was not seen when cells were exposed to long-R3-IGF-I.
In plain wordsIn prostate cancer cells grown in the lab, NKX3.1 did not dampen signaling driven by long-R3-IGF-I.
- Peptide
- IGF-1 LR3
- Outcome
- No significant changeNKX3.1 effect on IGF-I signaling with long-R3-IGF-I
- Study
n: not reported in source
PC-3 cells- Outcome group
- Receptor activity and mechanism · Cancer
Source sentences
The effect of NKX3.1 on IGF-I signaling was not seen when cells were exposed to long-R3-IGF-I, an IGF-I variant peptide that does not bind to IGFBP-3.
1 context sentence(design, population, supporting numbers)
NKX3.1 expression in PC-3 cells attenuated the ability of insulin-like growth factor-I (IGF-I) to induce phosphorylation of type I IGF receptor (IGF-IR), insulin receptor substrate 1, phosphatidylinositol 3-kinase, and AKT.
In this study, IGF-1 LR3 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking IGF-1 LR3.