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Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
The Role of p53 in Nanoparticle-Based Therapy for Cancer
Olga Szewczyk-Roszczenko1, Nikolai A Barlev2,3,4
1Department of Synthesis and Technology of Drugs, Medical University of Bialystok, Kilinskiego 1, 15-089 Bialystok, Poland.
Abstract:
p53 is arguably one of the most important tumor suppressor genes in humans. Due to the paramount importance of p53 in the onset of cell cycle arrest and apoptosis, the p53 gene is found either silenced or mutated in the vast majority of cancers. Furthermore, activated wild-type p53 exhibits a strong bystander effect, thereby activating apoptosis in surrounding cells without being physically present there. For these reasons, p53-targeted therapy that is designed to restore the function of wild-type p53 in cancer cells seems to be a very appealing therapeutic approach. Systemic delivery of p53-coding DNA or RNA using nanoparticles proved to be feasible both in vitro and in vivo. In fact, one p53-based therapeutic (gendicine) is currently approved for commercial use in China. However, the broad use of p53-based therapy in p53-inactivated cancers is severely restricted by its inadequate efficacy. This review highlights the current state-of-the-art in this area of biomedical research and also discusses novel approaches that may help overcome the shortcomings of p53-targeting nanomedicine.
Insights
Restoring tumor suppressor p53 gene function in cancer cells via nanomedicine shows promise. However, current p53-based therapies face efficacy challenges, necessitating novel approaches for broader clinical application.
Area of Science:
- Oncology
- Molecular Biology
- Nanomedicine
Background:
- The p53 gene is a critical human tumor suppressor, vital for cell cycle arrest and apoptosis.
- p53 mutations or silencing are prevalent in most cancers, highlighting its importance in cancer development.
- Activated wild-type p53 can induce apoptosis in neighboring cancer cells (bystander effect).
Purpose of the Study:
- To review the current advancements in p53-targeted cancer therapy using nanomedicine.
- To discuss novel strategies for enhancing the efficacy of p53-based nanomedicines.
- To address the limitations of current p53-targeting approaches in p53-inactivated cancers.
Main Methods:
- Systemic delivery of p53-coding DNA or RNA via nanoparticles.
- In vitro and in vivo feasibility studies of p53 nanomedicine.
- Review of existing literature on p53-based cancer therapeutics.
Main Results:
- Nanoparticle-mediated delivery of p53 DNA/RNA is feasible for cancer therapy.
- One p53-based therapy (gendicine) is approved in China.
- Current p53-based therapies exhibit inadequate efficacy in p53-inactivated cancers.
Conclusions:
- p53-targeted therapy is a promising strategy for cancer treatment due to p53's role in apoptosis.
- Overcoming efficacy limitations is crucial for the widespread clinical application of p53 nanomedicine.
- Further research into novel approaches is needed to improve p53-based cancer therapies.
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