Related Experiment Video
Updated: Aug 15, 2026

Assessment of Resistance to Tyrosine Kinase Inhibitors by an Interrogation of Signal Transduction Pathways by Antibody Arrays
Published on: September 19, 2018
[Role of phosphatidylinositol signalling path in developing hormonal resistance in tumor cells]
M A Krasil'nikov1, V A Shatskaia
1Research Institute of Carcinogenesis, N.N. Blokhin Center for Oncology Research, Russian Academy of Medical Sciences, Moscow.
Abstract:
Phosphatidylinositol 3-kinase (PI3K) is a key regulatory protein which is responsible for anti-apoptotic signal transduction regulating cell survival during exposure to damaging factors. The report deals with the role of the PI3K signaling pathway in regulating cellular response to hormones and, particularly, in development of resistance as a result of long-term exposure of cells to steroid cytostatic hormones. In our study, even a short-term exposure of transformed fibroblasts of hamster (line 2PK) resulted in an activation of main PI3K effectors (MAP-kinase and protein kinase B (PKB)) which appeared against the background of hormone-induced inhibition of cellular growth. A long-term (3 months) cell culturing with dexamethasone was followed by formation of subpopulations of cells which were refractory to the growth inhibition by hormone and were characterized by high levels of activity of PI3K, MAP-kinases and PKB. Activation of PI3K and PI3K-dependent enzymes correlated with enhancement of synthesis of c-jun, a component of the AP-1 transcriptional factor, was observed both in short- and long-term application of dexamethasone. We believe that, during long-term exposure of cells to cytostatic hormones, continuous activation of PI3K and PI3K-dependent transcriptional factors may result in a significant restructuring of intracellular signal pathway, and, finally, constitutive PI3K-signal pathway and partial overcoming the proliferative block by cells.
Insights
The phosphatidylinositol 3-kinase (PI3K) pathway regulates cell survival and hormone resistance. Long-term exposure to dexamethasone activates PI3K signaling, leading to cells that overcome growth inhibition.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Phosphatidylinositol 3-kinase (PI3K) is crucial for anti-apoptotic signaling and cell survival.
- The PI3K pathway regulates cellular responses to hormones, including the development of resistance to steroid cytostatic hormones.
Purpose of the Study:
- To investigate the role of the PI3K signaling pathway in cellular response to hormones.
- To understand the development of resistance to steroid cytostatic hormones through PI3K pathway modulation.
Main Methods:
- Exposure of transformed hamster fibroblasts (line 2PK) to dexamethasone for short-term and long-term periods.
- Analysis of PI3K effector activation (MAP-kinase, protein kinase B/PKB).
- Assessment of c-jun synthesis and AP-1 transcriptional factor activity.
Main Results:
- Short-term dexamethasone exposure activated PI3K effectors (MAP-kinase, PKB) despite growth inhibition.
- Long-term dexamethasone exposure (3 months) generated resistant cell subpopulations with high PI3K, MAP-kinase, and PKB activity.
- Dexamethasone treatment, short- or long-term, enhanced PI3K activity and c-jun synthesis, a component of AP-1.
Conclusions:
- Continuous PI3K activation by cytostatic hormones can restructure intracellular signaling.
- This leads to a constitutive PI3K pathway, enabling cells to partially overcome proliferative blocks.
- The PI3K pathway and its dependent transcription factors play a significant role in hormone resistance development.
Related Concept Videos
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Amplifying Signals via Second Messengers
PI3K/mTOR/AKT Signaling Pathway
IP3/DAG Signaling Pathway
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

