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Updated: Sep 22, 2025

Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
Advances in nanotechnology-based platforms for survivin-targeted drug discovery
Rosemol George1, Stephanie Hehlgans1, Maximillian Fleischmann1
1Department of Radiotherapy and Oncology, Goethe University, Frankfurt am Main, Germany.
Introduction:
Due to its unique functional impact on multiple cancer cell circuits including proliferation, apoptosis, tumor dissemination, DNA damage repair, and immune response, the inhibitor of apoptosis protein (IAP) survivin has gained high interest as a molecular target and a multitude of therapeutics were developed to interfere with survivin expression and functionality. First clinical evaluations of these therapeutics, however, were disappointing highlighting the need to develop advanced delivery systems of survivin-targeting therapeutics.
Areas Covered:
This review focuses on advancements in nanocarriers to molecularly target survivin in human malignancies. A plethora of nanoparticle platforms, including liposomes, polymeric systems, dendrimers, inorganic nanocarriers, RNA/DNA nanotechnology and exosomes, are discussed in the background of survivin-tailored RNA interference, small molecule inhibitors, dominant negative mutants or survivin vaccination or combined modality treatment with chemotherapeutic drugs and photo-dynamic/photothermal strategies.
Expert Opinion:
Novel therapeutic approaches include the use of biocompatible nanoformulations carrying gene silencing or drug molecules to directly or indirectly target proteins, allow for a more precise and controlled delivery of survivin therapeutics. Moreover, surface modification of these nanocarriers may result in a tumor entity-specific delivery. Therefore, nanomedicine exploiting survivin-tailored strategies in a multimodal background is considered the way forward to enhance the development of future personalized medicine.
Insights
Advanced nanocarriers show promise for delivering survivin-targeting cancer therapeutics. These novel systems aim to improve treatment efficacy by precisely targeting survivin, a key protein in cancer cell circuits.
Area of Science:
- Oncology
- Nanomedicine
- Molecular Biology
Background:
- Survivin, an inhibitor of apoptosis protein (IAP), is a key target in cancer due to its role in proliferation, apoptosis, DNA repair, and immune response.
- Previous survivin-targeting therapeutics faced clinical limitations, necessitating advanced delivery systems.
- Nanotechnology offers potential solutions for precise and controlled delivery of survivin therapeutics.
Purpose of the Study:
- To review advancements in nanocarriers for targeting survivin in human malignancies.
- To explore various nanoparticle platforms and their application in survivin-tailored therapies.
- To highlight the potential of nanomedicine in developing personalized cancer treatments.
Main Methods:
- Review of nanoparticle platforms including liposomes, polymeric systems, dendrimers, inorganic nanocarriers, RNA/DNA nanotechnology, and exosomes.
- Discussion of survivin-tailored strategies such as RNA interference, small molecule inhibitors, dominant negative mutants, and vaccination.
- Exploration of combination therapies involving nanocarriers with chemotherapy and photodynamic/photothermal strategies.
Main Results:
- Nanocarriers enable precise and controlled delivery of gene silencing or drug molecules to target survivin.
- Surface modification of nanocarriers can achieve tumor entity-specific delivery.
- Multimodal nanomedicine strategies exploiting survivin targeting show promise for enhancing therapeutic outcomes.
Conclusions:
- Nanomedicine offers a promising approach to overcome limitations of conventional survivin-targeting therapeutics.
- Advanced nanocarrier systems facilitate targeted delivery and enhanced efficacy of survivin-tailored treatments.
- Exploiting nanomedicine for survivin targeting in a multimodal context is crucial for advancing personalized cancer medicine.
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