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Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery
Published on: May 2, 2019
siRNA-based Nanocarriers for Targeted Therapy in Prostate Cancer: Implications for Male Fertility Preservation
Krishna Kant Jangde1, Rajeev Shrama2, Dinesh Kumar Mishra1
1Department of Pharmacy, Guru Ghasidas Vishwavidyalaya (A Central University), Bilaspur, Chhattisgarh, India.
Abstract:
Prostate cancer (PC), a significant global health burden, is further complicated by therapeutic resistance, systemic toxicity, and adverse effects on male fertility associated with conventional treatments. Small interfering RNA (siRNA)-based therapeutics offer molecular precision in oncogene silencing and tumor-promoting pathways. However, their clinical translation is constrained by challenges related to stability, delivery, and cellular uptake. Nanocarriers, including lipid-based, exosome-based, and other polymeric-based systems, could enhance stability, specificity, and efficacy. In this review, we highlight biomarker-targeted siRNA codelivery for PC, considering reproductive health and translational barriers, highlighting the future of fertility-preserving and quality of life-oriented therapies.
Insights
Small interfering RNA (siRNA) therapies show promise for prostate cancer (PC) but face delivery challenges. Nanocarriers can improve siRNA stability and efficacy, paving the way for fertility-preserving treatments.
Area of Science:
- Oncology
- Nanotechnology
- Biotechnology
Background:
- Prostate cancer (PC) presents a significant global health challenge, with conventional treatments often leading to therapeutic resistance, toxicity, and male infertility.
- Small interfering RNA (siRNA) therapeutics offer precise targeting of oncogenes and tumor-promoting pathways, but clinical application is hindered by issues with stability, delivery, and cellular uptake.
Purpose of the Study:
- To review the potential of biomarker-targeted siRNA codelivery systems for prostate cancer treatment.
- To explore how nanocarriers can overcome the limitations of siRNA delivery.
- To consider the impact on reproductive health and identify future directions for fertility-preserving therapies.
Main Methods:
- Literature review focusing on siRNA-based therapeutics, nanocarrier systems (lipid-based, exosome-based, polymeric), and their application in prostate cancer.
- Analysis of strategies for biomarker-targeted codelivery of siRNA.
- Evaluation of translational barriers and their impact on clinical application and reproductive health.
Main Results:
- Nanocarriers demonstrate potential to enhance the stability, specificity, and efficacy of siRNA therapeutics for prostate cancer.
- Biomarker-targeted codelivery strategies are emerging as a promising approach.
- Addressing translational barriers is crucial for clinical success and patient quality of life.
Conclusions:
- Nanocarrier-mediated siRNA codelivery holds significant promise for advancing prostate cancer treatment.
- Future research should focus on optimizing delivery systems and addressing reproductive health concerns to develop more effective and patient-centered therapies.
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