Investigation of the Role of Glucose Decorated Chitosan and PLGA Nanoparticles as Blocking Agents to Glucose Transporters of Tumor Cells

References

• Bahrami B, Hojjat-Farsangi M, Mohammadi H, et al. Nanoparticles and targeted drug delivery in cancer therapy. Immunol Lett. 2017;190:64–83. doi:10.1016/j.imlet.2017.07.01528760499
   PubMed Web of Science ®Google Scholar
• Ge Y, Ma Y, Li L. The application of prodrug-based nano-drug delivery strategy in cancer combination therapy. Colloids Surf B Biointerfaces. 2016;146:482–489. doi:10.1016/j.colsurfb.2016.06.05127400243
   PubMedGoogle Scholar
• Mokhtarzadeh A, Hassanpour S, Vahid ZF, et al. Nano-delivery system targeting to cancer stem cell cluster of differentiation biomarkers. J Control Release. 2017;266:166–186. doi:10.1016/j.jconrel.2017.09.02828941992
   PubMed Web of Science ®Google Scholar
• Raavé R, van Kuppevelt TH, Daamen WF. Chemotherapeutic drug delivery by tumoral extracellular matrix targeting. J Control Release. 2018;274:1–8. doi:10.1016/j.jconrel.2018.01.02929382546
   PubMed Web of Science ®Google Scholar
• Thanuja MY, Anupama C, Ranganath SH. Bioengineered cellular and cell membrane-derived vehicles for actively targeted drug delivery: so near and yet so far. Adv Drug Deliv Rev. 2018;132:57–8029935987
   PubMed Web of Science ®Google Scholar
• Parks SK, Cormerais Y, Marchiq I, Pouyssegur J. Hypoxia optimises tumour growth by controlling nutrient import and acidic metabolite export. Mol Aspects Med. 2016;47–48:3–14. doi:10.1016/j.mam.2015.12.001
   PubMed Web of Science ®Google Scholar
• Warburg O, Wind F, Negelein E. The metabolism of tumors in the body. J Gen Physiol. 1927;8(6):519–530. doi:10.1085/jgp.8.6.51919872213
   PubMedGoogle Scholar
• Barron CC, Bilan PJ, Tsakiridis T, Tsiani E. Facilitative glucose transporters: implications for cancer detection, prognosis and treatment. Metabolism. 2016;65(2):124–139. doi:10.1016/j.metabol.2015.10.00726773935
   PubMed Web of Science ®Google Scholar
• Montiel Schneider MG, Martin MJ, Coral DF, et al. Selective contrast agents with potential to the earlier detection of tumors: insights on synthetic pathways, physicochemical properties and performance in MRI assays. Colloids Surf B Biointerfaces. 2018;170:470–478. doi:10.1016/j.colsurfb.2018.06.04429960215
   PubMedGoogle Scholar
• Liu D-Z, Sinchaikul S, Reddy PVG, Chang M-Y, Chen S-T. Synthesis of 2′-paclitaxel methyl 2-glucopyranosyl succinate for specific targeted delivery to cancer cells. Bioorg Med Chem Lett. 2007;17(3):617–620. doi:10.1016/j.bmcl.2006.11.00817113288
   PubMedGoogle Scholar
• Wu M, Li H, Liu R, et al. Galactose conjugated platinum(II) complex targeting the Warburg effect for treatment of non-small cell lung cancer and colon cancer. Eur J Med Chem. 2016;110:32–42. doi:10.1016/j.ejmech.2016.01.01626807543
   PubMed Web of Science ®Google Scholar
• Gao X, Liu S, Shi Y, et al. Mechanistic and biological characteristics of different sugar conjugated 2-methyl malonatoplatinum(II) complexes as new tumor targeting agents. Eur J Med Chem. 2017;125:372–384. doi:10.1016/j.ejmech.2016.09.04727688191
   PubMedGoogle Scholar
• Jiang X, Xin H, Ren Q, et al. Nanoparticles of 2-deoxy-d-glucose functionalized poly(ethylene glycol)-co-poly(trimethylene carbonate) for dual-targeted drug delivery in glioma treatment. Biomaterials. 2014;35(1):518–529. doi:10.1016/j.biomaterials.2013.09.09424125772
   PubMed Web of Science ®Google Scholar
• Asik E, Aslan TN, Volkan M, Guray NT. 2-Amino-2-deoxy-glucose conjugated cobalt ferrite magnetic nanoparticle (2DG-MNP) as a targeting agent for breast cancer cells. Environ Toxicol Pharmacol. 2016;41:272–278. doi:10.1016/j.etap.2015.12.00426761626
   PubMed Web of Science ®Google Scholar
• Li J, Ma F-K, Dang Q-F, Liang X-G, Chen X-G. Glucose-conjugated chitosan nanoparticles for targeted drug delivery and their specific interaction with tumor cells. Front Mater Sci. 2014;8(4):363–372. doi:10.1007/s11706-014-0262-8
   Web of Science ®Google Scholar
• Vunain E, Mishra AK, Mamba BB. 1 - Fundamentals of chitosan for biomedical applications In: Jennings JA, Bumgardner JD, editors. Chitosan Based Biomaterials. Vol. 1 Woodhead Publishing; 2017:3–30.
   Google Scholar
• Choi C, Nam J-P, Nah J-W. Application of chitosan and chitosan derivatives as biomaterials. J Ind Eng Chem. 2016;33:1–10. doi:10.1016/j.jiec.2015.10.028
   Web of Science ®Google Scholar
• Vyas R, Gupta N, Nimesh S. Chapter 9 - Chitosan nanoparticles for efficient and targeted delivery of anticancer drugs In: Grumezescu AM, editor. Nanobiomaterials in Cancer Therapy. William Andrew Publishing; 2016:281–306.
   Google Scholar
• Fonseca-Santos B, Chorilli M. An overview of carboxymethyl derivatives of chitosan: their use as biomaterials and drug delivery systems. Mater Sci Eng C. 2017;77:1349–1362. doi:10.1016/j.msec.2017.03.198
   PubMed Web of Science ®Google Scholar
• Mir M, Ahmed N, Rehman A. Recent applications of PLGA based nanostructures in drug delivery. Colloids Surf B Biointerfaces. 2017;159:217–231. doi:10.1016/j.colsurfb.2017.07.03828797972
   PubMed Web of Science ®Google Scholar
• Son J, Yang SM, Yi G, et al. Folate-modified PLGA nanoparticles for tumor-targeted delivery of pheophorbide a in vivo. Biochem Biophys Res Commun. 2018;498(3):523–528. doi:10.1016/j.bbrc.2018.03.01329518390
   PubMedGoogle Scholar
• Calvo P, Remuñán-López C, Vila-Jato JL, Alonso MJ. Novel hydrophilic chitosan-polyethylene oxide nanoparticles as protein carriers. J Appl Poly Sci. 1997;63(1):125–132. doi:10.1002/(SICI)1097-4628(19970103)63:1<125::AID-APP13>3.0.CO;2-4
   Web of Science ®Google Scholar
• Xiguang Chen JL, Cheng X, Inventor TJ. Process for preparing compounds of chitosan saccharified with aminosugar. 2008.
   Google Scholar
• Pereira C, Costa J, Sarmento B, Araújo F. 3.3 - Cell-based in vitro models for intestinal permeability studies In: Sarmento B, editor. Concepts and Models for Drug Permeability Studies. Woodhead Publishing; 2016:57–81.
   Google Scholar
• Adlin Jino J. Nesalin AAS. Preparation and evaluation of chitosan nanoparticles containing zidovudine. Asian J Pharm Sci. 2012;7(1):80–84.
   Google Scholar
• Abolhasani H, Zarghi A, Abolhasani A, et al. Design, synthesis and in vitro cytotoxicity evaluation of new 3’,4’-bis (3,4,5-trisubstituted)-4’H-spiro[indene-2,5’-isoxazol]-1(3H)-one derivatives as promising anticancer agents. Lett Drug Des Discov. 2014;11(10):1149–1161. doi:10.2174/1570180811666140704172442
   Web of Science ®Google Scholar
• Abolhasani A, Heidari F, Noori S, Mousavi S, Abolhasani H. Cytotoxicity evaluation of dimethoxy and trimethoxy indanonic spiroisoxazolines against cancerous liver cells. Curr Chem Biol. 2019;13(3).
   Google Scholar
• Wang X, Yang L, Zhang H, et al. Fluorescent magnetic PEI-PLGA nanoparticles loaded with paclitaxel for concurrent cell imaging, enhanced apoptosis and autophagy in human brain cancer. Colloids Surf B Biointerfaces. 2018;172:708–717. doi:10.1016/j.colsurfb.2018.09.03330245296
   PubMed Web of Science ®Google Scholar
• Rescignano N, Tarpani L, Romani A, et al. In-vitro degradation of PLGA nanoparticles in aqueous medium and in stem cell cultures by monitoring the cargo fluorescence spectrum. Polym Degrad Stab. 2016;134:296–304. doi:10.1016/j.polymdegradstab.2016.10.017
   Web of Science ®Google Scholar
• Sena P, Mancini S, Benincasa M, Mariani F, Palumbo C, Roncucci L. Metformin induces apoptosis and alters cellular responses to oxidative stress in Ht29 colon cancer cells: preliminary findings. Int J Mol Sci. 2018;19:5. doi:10.3390/ijms19051478
   Web of Science ®Google Scholar
• Alarifi S, Ali H, Alkahtani S, Alessia MS. Regulation of apoptosis through bcl-2/bax proteins expression and DNA damage by nano-sized gadolinium oxide. Int J Nanomedicine. 2017;12:4541–4551. doi:10.2147/IJN.S13932628684914
   PubMed Web of Science ®Google Scholar
• Montel-Hagen A, Blanc L, Boyer-Clavel M, et al. The Glut1 and Glut4 glucose transporters are differentially expressed during perinatal and postnatal erythropoiesis. Blood. 2008;112(12):4729. doi:10.1182/blood-2008-05-15926918796630
   PubMedGoogle Scholar
• Calvo MB, Figueroa A, Pulido EG, Campelo RG, Aparicio LA. Potential role of sugar transporters in cancer and their relationship with anticancer therapy. Int J Endocrinol. 2010;2010:14. doi:10.1155/2010/205357
   Web of Science ®Google Scholar
• Swider E, Staal AHJ, Koen van Riessen N, et al. Design of triphasic poly(lactic-co-glycolic acid) nanoparticles containing a perfluorocarbon phase for biomedical applications. RSC Adv. 2018;8(12):6460–6470. doi:10.1039/C7RA13062G
   PubMed Web of Science ®Google Scholar
• Wan S, Zhang L, Quan Y, Wei K. Resveratrol-loaded PLGA nanoparticles: enhanced stability, solubility and bioactivity of resveratrol for non-alcoholic fatty liver disease therapy. R Soc Open Sci. 2018;5:181457. doi:10.1098/rsos.18145730564426
   PubMed Web of Science ®Google Scholar
• Barbosa AI, Costa Lima SA, Reis S. Application of pH-responsive fucoidan/chitosan nanoparticles to improve oral quercetin delivery. Molecules. 2019;24(2):346. doi:10.3390/molecules24020346
   PubMed Web of Science ®Google Scholar
• Maryam K, Azarpanah A. Preparation and in vitro evaluation of chitosan nanoparticles containing diclofenac using the ion-gelation method. Jundishapur J Nat Pharm Prod. 2015;10:1–7.
   Google Scholar
• Zambrano A, Molt M, Uribe E, Salas M. Glut 1 in cancer cells and the inhibitory action of resveratrol as a potential therapeutic strategy. Int J Mol Sci. 2019;20(13):3374. doi:10.3390/ijms20133374
   PubMed Web of Science ®Google Scholar
• Granchi C, Fortunato S, Minutolo F. Anticancer agents interacting with membrane glucose transporters. MedChemComm. 2016;7(9):1716–1729. doi:10.1039/C6MD00287K28042452
   PubMedGoogle Scholar
• Zhang W, Liu Y, Chen X, Bergmeier SC. Novel inhibitors of basal glucose transport as potential anticancer agents. Bioorg Med Chem Lett. 2010;20(7):2191–2194. doi:10.1016/j.bmcl.2010.02.02720194024
   PubMed Web of Science ®Google Scholar
• Airley RE, Mobasheri A. Hypoxic regulation of glucose transport, anaerobic metabolism and angiogenesis in cancer: novel pathways and targets for anticancer therapeutics. Chemotherapy. 2007;53(4):233–256. doi:10.1159/00010445717595539
   PubMed Web of Science ®Google Scholar
• Choudhry H, Harris AL. Advances in hypoxia-inducible factor biology. Cell Metab. 2018;27(2):281–298. doi:10.1016/j.cmet.2017.10.00529129785
   PubMed Web of Science ®Google Scholar
• Lv X, Li J, Zhang C, et al. The role of hypoxia-inducible factors in tumor angiogenesis and cell metabolism. Genes Dis. 2017;4(1):19–24. doi:10.1016/j.gendis.2016.11.00330258904
   PubMed Web of Science ®Google Scholar