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Chitosan nanoparticles as a dual drug/siRNA delivery system for treatment of colorectal cancer
Abstract
Nanoparticles are widely used to deliver anticancer drugs and inhibit tumor growth without systemic toxicity. Recently, chitosan has received much attention as a functional biopolymer for encapsulation of small interfering RNA (siRNA). Because of cationic nature, chitosan efficiently encapsulate siRNA and forming nanoparticles. Moreover, biocompatible and biodegradable properties represent chitosan as potential candidate for in vivo siRNA delivery. In the present study we designed carboxymethyl dextran (CMD) chitosan nanoparticles (ChNPs) to encapsulate snail siRNA and anticancer drug doxorubicin (DOX). The effect of ChNPs-drug/siRNA on cell growth and Epithelial mesenchymal transition (EMT) gene expression of HCT-116 cell lines were investigated. Furthermore the efficacy of dual agent nanoparticle to induce apoptosis and inhibit migration of colorectal cancer cells were assessed using Annexin-V and wound healing assays, respectively. The results demonstrated that treatment with dual agent nanoparticles led to significant changes of EMT genes (i.e down regulation of MMP-9 and Vimentin and up regulation of E-cadherin), apoptosis cell death and migration inhibition in HCT-116 cells. In conclusion, ChNPs encapsulating DOX and snail siRNA can be considered as an effective anti-cancer drugs delivery system for the treatment of colorectal cancer.
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“Delivering snail siRNA and doxorubicin via CSNPs led to significant changes of Epithelial mesenchymal transition genes as (Down regulation the expression of Vimentin and MMP-9 and upregulation of E-cadherin) well as inhibited growth, migration and induced apoptosis cell death of HCT-116 cells.”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [197]
Citations
Cites
New functions for the matrix metalloproteinases in cancer progression
Egeblad, M., & Werb, Z. (2002) · Nature Reviews Cancer · doi:10.1038/nrc745 · Cited by 6,108
Drug penetration in solid tumours
Minchinton, A. I., & Tannock, I. F. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1893 · Cited by 2,805
Doxorubicin: The good, the bad and the ugly effect
Carvalho, C., Santos, R., Cardoso, S., Correia, S., Oliveira, P., Santos, M., & Moreira, P. (2009) · Current Medicinal Chemistry · doi:10.2174/092986709788803312 · Cited by 1,509
Research works printed but not linked: 26
- Hosseinzadeh, 2012, Chitosan-pluronic nanoparticles as oral delivery of anticancer gemcitabine: preparation and in vitro study, Int. J. Nanomed., 7, 1851
- Suri, 2007, Nanotechnology-based drug delivery systems, J. Occup. Med. Toxicol., 2, 16, 10.1186/1745-6673-2-16 · DOI
- Bahrami, 2015, Folate-conjugated nanoparticles as a potent therapeutic approach in targeted cancer therapy, Tumor Biol., 36, 5727, 10.1007/s13277-015-3706-6 · DOI
- Wang, 2011, Recent advances of chitosan nanoparticles as drug carriers, Int. J. Nanomed., 6, 765
- Shi, 2002, Advances in nanoparticle system for deliverying drugs across the biological barriers, J. China Pharm. Univ., 33, 169
- Dolati, 2016, Utilization of nanoparticle technology in rheumatoid arthritis treatment, Biomed. Pharmacother., 80, 30, 10.1016/j.biopha.2016.03.004 · DOI
- Ayala, 2013, Effect of surface charge on the colloidal stability and in vitro uptake of carboxymethyl dextran-coated iron oxide nanoparticles, J. Nanopart. Res., 15, 1, 10.1007/s11051-013-1874-0 · DOI
- Mikhaylov, 2011, Promising approaches in using magnetic nanoparticles in oncology, Biol. Chem., 392, 955, 10.1515/BC.2011.185 · DOI
- Wilhelm, 2003, Intracellular uptake of anionic superparamagnetic nanoparticles as a function of their surface coating, Biomaterials, 24, 1001, 10.1016/S0142-9612(02)00440-4 · DOI
- Jere, 2009, Chitosan-graft-polyethylenimine for Akt1 siRNA delivery to lung cancer cells, Int. J. Pharm., 378, 194, 10.1016/j.ijpharm.2009.05.046 · DOI
- Kachalaki, 2015, Reversal of chemoresistance with small interference RNA (siRNA) in etoposide resistant acute myeloid leukemia cells (HL-60), Biomed. Pharmacother., 75, 100, 10.1016/j.biopha.2015.08.032 · DOI
- Park, 2009, Biodegradable luminescent porous silicon nanoparticles for in vivo applications, Nat. Mater., 8, 331, 10.1038/nmat2398 · DOI
- Ajaj, 2009, In vitro and in vivo study of an albumin-binding prodrug of doxorubicin that is cleaved by cathepsin B, Cancer Chemother. Pharmacol., 64, 413, 10.1007/s00280-009-0942-8 · DOI
- Qi, 2010, Nanoparticles with dextran/chitosan shell and BSA/chitosan core—doxorubicin loading and delivery, Int. J. Pharm., 393, 177, 10.1016/j.ijpharm.2010.03.063 · DOI
- Zucker, 2004, Role of matrix metalloproteinases (MMPs) in colorectal cancer, Cancer Metastasis Rev., 23, 101, 10.1023/A:1025867130437 · DOI
- Satelli, 2011, Vimentin in cancer and its potential as a molecular target for cancer therapy, Cell. Mol. Life Sci., 68, 3033, 10.1007/s00018-011-0735-1 · DOI
- Ngan, 2007, Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer, Br. J. Cancer, 96, 986, 10.1038/sj.bjc.6603651 · DOI
- Batlle, 2000, The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cells, Nat. Cell Biol., 2, 84, 10.1038/35000034 · DOI
- Eivazy, 2016, The impact of the codelivery of drug-siRNA by trimethyl chitosan nanoparticles on the efficacy of chemotherapy for metastatic breast cancer cell line (MDA-MB-231), Artif. Cells Nanomed. Biotechnol., 1, 10.1080/21691401.2016.1185727 · DOI
- Jadidi-Niaragh, 2016, Downregulation of CD73 in 4T1 breast cancer cells through siRNA-loaded chitosan-lactate nanoparticles, Tumor Biol., 1
- Massing, 2000, Liposomal formulations of anticancer drugs: selectivity and effectiveness, Drug Resist. Updates, 3, 171, 10.1054/drup.2000.0138 · DOI
- Mu, 2003, A novel controlled release formulation for the anticancer drug paclitaxel (Taxol®): PLGA nanoparticles containing vitamin E TPGS, J. Control. Release, 86, 33, 10.1016/S0168-3659(02)00320-6 · DOI
- Verdun, 1990, Tissue distribution of doxorubicin associated with polyisohexylcyanoacrylate nanoparticles, Cancer Chemother. Pharmacol., 26, 13, 10.1007/BF02940287 · DOI
- Orlichenko, 2008, Matrix metalloproteinases stimulate epithelial-mesenchymal transition during tumor development, Clin. Exp. Metastasis, 25, 593, 10.1007/s10585-008-9143-9 · DOI
- Jordà, 2005, Upregulation of MMP-9 in MDCK epithelial cell line in response to expression of the Snail transcription factor, J. Cell Sci., 118, 3371, 10.1242/jcs.02465 · DOI
- Jin, 2010, Snail is critical for tumor growth and metastasis of ovarian carcinoma, Int. J. Cancer, 126, 2102, 10.1002/ijc.24901 · DOI
Cited by
Sorted by citations
Hossain, M. S., Karuniawati, H., Jairoun, A. A., Urbi, Z., Ooi, D. J., John, A., Lim, Y. C., Kibria, K. M. K., Mohiuddin, A. K. M., Ming, L. C., et al. (2022) · Cancers · doi:10.3390/cancers14071732 · Cited by 920
Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment
Choukaife, H., Seyam, S., Alallam, B., Doolaanea, A. A., & Alfatama, M. (2022) · International Journal of Nanomedicine · doi:10.2147/ijn.s375229 · Cited by 127
Sun, Y., Zhao, Y., Zhao, X., Lee, R. J., Teng, L., & Zhou, C. (2017) · Molecules · doi:10.3390/molecules22101724 · Cited by 56
Metadata
- Authors
- Sadreddini, S., Safaralizadeh, R., Baradaran, B., Aghebati-Maleki, L., Hosseinpour-Feizi, M. A., Shanehbandi, D., Jadidi-Niaragh, F., Sadreddini, S., Kafil, H. S., Younesi, V., & Yousefi, M.
- Venue
- Immunology Letters
- Publisher
- Elsevier BV
- Published
- 2017-01
- Volume
- 181
- Pages
- 79-86
- ISSN
- 0165-2478
- Cited by
- 101
- References
- 3
- Language
- en
- Funders
- Immunology Research Center, Tabriz University of Medical Sciences (93-76)
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