Literature DB >> 34072925

Development of a Rapid-Onset, Acid-Labile Linkage Polyplex-Mixed Micellar System for Anticancer Therapy.

Shiou-Fen Hung1, Yu-Han Wen1, Lu-Yi Yu1, Hsin-Cheng Chiu2, Yi-Ting Chiang3, Chun-Liang Lo1.   

Abstract

In the treatment of cancers, small interfering ribonucleic acids (siRNAs) are delivered into cells to inhibit the oncogenic protein's expression; however, polyanions, hydrophilicity, and rapid degradations in blood, endosomal or secondary lysosomal degradation hamper clinal applications. In this study, we first synthesized and characterized two copolymers: methoxy poly(ethylene glycol)-b-poly(2-hydroxy methacrylate-ketal-pyridoxal) and methoxy poly(ethylene glycol)-b-poly(methacrylic acid-co-histidine). Afterwards, we assembled two polymers with the focal adhesion kinase (FAK) siRNA, forming polyplex-mixed micelles for the treatment of the human colon cancer cell line HCT116. In terms of the physiological condition, the cationic pyridoxal molecules that were conjugated on the copolymer with ketal bonds could electrostatically attract the siRNA. Additionally, the pyridoxal could form a hydrophobic core together with the hydrophobic deprotonated histidine molecules in the other copolymer and the hydrophilic polyethylene glycol (PEG) shell to protect the siRNA. In an acidic condition, the pyridoxal would be cleaved from the polymers due to the breakage of the ketal bonds and the histidine molecules can simultaneously be protonated, resulting in the endosome/lysosome escape effect. On the basis of our results, the two copolymers were successfully prepared and the pyridoxal derivatives were identified to be able to carry the siRNA and be cleavable by the copolymers in an acidic solution. Polyplex-mixed micelles were prepared, and the micellar structures were identified. The endosome escape behavior was observed using a confocal laser scanning microscopy (CLSM). The FAK expression was therefore reduced, and the cytotoxicity of siRNA toward human colon cancer cells was exhibited, rapidly in 24 h. This exceptional anticancer efficiency suggests the potential of the pH-sensitive polyplex-mixed micellar system in siRNA delivery.

Entities:  

Keywords:  acid-labile; anticancer therapy; mixed micelle; siRNA delivery

Year:  2021        PMID: 34072925     DOI: 10.3390/polym13111823

Source DB:  PubMed          Journal:  Polymers (Basel)        ISSN: 2073-4360            Impact factor:   4.329


  34 in total

Review 1.  The current state and future directions of RNAi-based therapeutics.

Authors:  Ryan L Setten; John J Rossi; Si-Ping Han
Journal:  Nat Rev Drug Discov       Date:  2019-06       Impact factor: 84.694

Review 2.  Overcoming cellular barriers for RNA therapeutics.

Authors:  Steven F Dowdy
Journal:  Nat Biotechnol       Date:  2017-02-27       Impact factor: 54.908

3.  Harnessing pH-Sensitive Polycation Vehicles for the Efficient siRNA Delivery.

Authors:  Changrong Wang; Xiaoxia Wang; Lili Du; Yanliang Dong; Bo Hu; Junhui Zhou; Yongli Shi; Suping Bai; Yuanyu Huang; Huiqing Cao; Zicai Liang; Anjie Dong
Journal:  ACS Appl Mater Interfaces       Date:  2021-01-06       Impact factor: 9.229

Review 4.  Quo vadis polyplex?

Authors:  Olivia M Merkel; Thomas Kissel
Journal:  J Control Release       Date:  2014-06-13       Impact factor: 9.776

Review 5.  Rekindling RNAi Therapy: Materials Design Requirements for In Vivo siRNA Delivery.

Authors:  Byungji Kim; Ji-Ho Park; Michael J Sailor
Journal:  Adv Mater       Date:  2019-09-30       Impact factor: 30.849

6.  Solvent-driven, self-assembled acid-responsive poly(ketalized serine)/siRNA complexes for RNA interference.

Authors:  Shirley Wong; Jessica A Kemp; Min Suk Shim; Young Jik Kwon
Journal:  Biomater Sci       Date:  2020-10-28       Impact factor: 6.843

Review 7.  Recent Advances of Polycationic siRNA Vectors for Cancer Therapy.

Authors:  Raut Bholakant; Hongliang Qian; Junmei Zhang; Xin Huang; Dechun Huang; Jan Feijen; Yinan Zhong; Wei Chen
Journal:  Biomacromolecules       Date:  2020-07-07       Impact factor: 6.988

Review 8.  Focal adhesion kinase: in command and control of cell motility.

Authors:  Satyajit K Mitra; Daniel A Hanson; David D Schlaepfer
Journal:  Nat Rev Mol Cell Biol       Date:  2005-01       Impact factor: 94.444

9.  Lipidic carriers of siRNA: differences in the formulation, cellular uptake, and delivery with plasmid DNA.

Authors:  Sebastien Spagnou; Andrew D Miller; Michael Keller
Journal:  Biochemistry       Date:  2004-10-26       Impact factor: 3.162

10.  Biophysical and structural characterization of polyethylenimine-mediated siRNA delivery in vitro.

Authors:  Amy C Richards Grayson; Anne M Doody; David Putnam
Journal:  Pharm Res       Date:  2006-08       Impact factor: 4.580

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