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Updated: Jun 16, 2026

Mimicking the Function of Signaling Proteins: Toward Artificial Signal Transduction Therapy
Published on: September 29, 2016
[Proliferation signal inhibitors: what therapeutic protocols are followed in 2009?]
1CHU Nancy, Hôpital d'adultes de Brabois, Service de néphrologie, Avenue de Bourgogne, Vandoeuvre Les Nancy, France. m.ladriere@chu-nancy.fr
Abstract:
Proliferation signal inhibitors (PSI) have been used in France for kidney transplants for some ten years. They provide a certain number of long-term benefits for kidney function in transplant patients due to their anti-proliferation and anti-tumour properties and absence of nephrotoxicity. Their use has been evaluated in therapeutic regimens aimed at reducing the nephrotoxicity associated with calcineurin inhibitors (CNI). Strategies based on minimizing the use of CNIs and therapy switches between 3 and 6 months have shown promising results, especially in terms of prevention of deterioration of kidney function. The best time to make the switch has not yet been defined with certainty, but predictors of success, preservation of good kidney function and absence of proteinuria have been established. Aside from cases of demonstrated CNI toxicity, a history or onset of de novo cancer is a situation in which this type of regimen can be considered.
Insights
Proliferation signal inhibitors (PSI) offer long-term benefits for kidney transplant recipients, preserving kidney function. Switching from calcineurin inhibitors (CNI) to PSI regimens shows promise in preventing kidney function decline.
Area of Science:
- Nephrology
- Immunosuppression
- Transplantation
Context:
- Proliferation signal inhibitors (PSI) have been utilized in France for kidney transplantation for approximately a decade.
- These agents offer benefits such as anti-proliferation, anti-tumor properties, and lack of nephrotoxicity, contributing to long-term kidney function preservation in transplant patients.
- Their application has been explored in therapeutic strategies to mitigate the nephrotoxicity associated with calcineurin inhibitors (CNI).
Purpose:
- To evaluate the efficacy of PSI in kidney transplant recipients.
- To assess strategies involving CNI minimization and therapy switching to PSI for improved kidney function.
- To identify predictors of successful outcomes in such therapeutic regimens.
Summary:
- Therapeutic regimens minimizing calcineurin inhibitor (CNI) use and incorporating switches to proliferation signal inhibitors (PSI) between 3 and 6 months post-transplant demonstrate positive outcomes.
- These strategies are particularly effective in preventing the deterioration of kidney function.
- Key predictors of success include the preservation of good kidney function and the absence of proteinuria, although the optimal timing for switching therapies requires further definition.
Impact:
- These findings suggest that PSI-based regimens can be a valuable option for managing kidney transplant patients, especially those with or at risk of CNI toxicity.
- The approach aids in preserving long-term kidney function and may be considered in cases of de novo cancer development.
- Further research into the precise timing of therapy switches can optimize patient outcomes and enhance the long-term success of kidney transplantation.
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