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Recent Advances in Preclinical Research Using PAMAM Dendrimers for Cancer Gene Therapy

Journal

Publisher

MDPI
DOI: 10.3390/ijms22062912

Keywords

PAMAM dendrimer; nanoparticles; cancer; gene therapy; gene delivery; nucleic acids; RNA delivery; small and large DNA; delivery systems; preclinical research

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Carriers of genetic material can be viral or non-viral, with non-viral carriers like PAMAM dendrimers showing promise in gene therapy due to their unique physiochemical properties and modification strategies. However, regulatory issues and limitations in clinical translation still need to be addressed for their broad implementation. Further research and improvements are crucial for the development of PAMAM dendrimers as carriers of genetic material in anticancer gene therapies.
Carriers of genetic material are divided into vectors of viral and non-viral origin. Viral carriers are already successfully used in experimental gene therapies, but despite advantages such as their high transfection efficiency and the wide knowledge of their practical potential, the remaining disadvantages, namely, their low capacity and complex manufacturing process, based on biological systems, are major limitations prior to their broad implementation in the clinical setting. The application of non-viral carriers in gene therapy is one of the available approaches. Poly(amidoamine) (PAMAM) dendrimers are repetitively branched, three-dimensional molecules, made of amide and amine subunits, possessing unique physiochemical properties. Surface and internal modifications improve their physicochemical properties, enabling the increase in cellular specificity and transfection efficiency and a reduction in cytotoxicity toward healthy cells. During the last 10 years of research on PAMAM dendrimers, three modification strategies have commonly been used: (1) surface modification with functional groups; (2) hybrid vector formation; (3) creation of supramolecular self-assemblies. This review describes and summarizes recent studies exploring the development of PAMAM dendrimers in anticancer gene therapies, evaluating the advantages and disadvantages of the modification approaches and the nanomedicine regulatory issues preventing their translation into the clinical setting, and highlighting important areas for further development and possible steps that seem promising in terms of development of PAMAM as a carrier of genetic material.

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