Anti Wnt-1 Monoclonal Antibody’s Conjugated with Gold Nanoparticles, Induced Apoptosis on MCF-7 Breast Cancer Cell Lines

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Wnt-β Catenin pathway has an important role in many cancers. Wnt-1 protein from the Wnt protein family, which regulates this pathway, has a special effect on the development of breast cancer. Monoclonal antibodies attaching to metal nanoparticles have an important role in the diagnosis and treatment of cancers.In this study, the anti-Wnt-1monoclonal antibody was conjugated to the gold nanoparticles synthesized by theTurkevichmethod. Conjugation was achieved using the EDC-NHS method. The density of the monoclonal antibodies bonded to gold nanoparticles was measured by Roche Cobas Integra 400 Plus device. MCF-7 and MDA-MB-231 breast cancer cell lines were treated with conjugated nanoparticles for 48 h, followed by performing a double-staining method to detect apoptosis cells.The results showed that inhibition of Wnt-1 protein in extracellular matrix causes apoptosis and gold nanoparticles to have a positive effect on Anti-Wnt-1monoclonal antibodies, leading to an increase in the number of conjugating nanoparticles.

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June 2019

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[1] D.C. Radisky, Epithelial-mesenchymal transition. J. Cell. Sci. 118 (2005) 4325-4326.

Google Scholar

[2] J.P. Thiery, H. Aclogue, R.Y.J. Huang, M. Angela Nieto, Epithelial-mesenchymal transitions in development and disease. Cell. 139 (2009) 871-890.

DOI: 10.1016/j.cell.2009.11.007

Google Scholar

[3] K. Polyak, R.A. Weinberg, Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits. Nat. Rev. Cancer. 9 (2009) 265-273.

DOI: 10.1038/nrc2620

Google Scholar

[4] R. Amerongen, R. Nusse, Towards an integrated view of Wnt signaling in development. Development. 136 (2009) 3205-3214.

DOI: 10.1242/dev.033910

Google Scholar

[5] B. Lustig, J. Behrens, The Wnt signaling pathway and its role in tumor development. J. Cancer. Res. Clin. Oncol. 129‏ (2003) 199-221.

DOI: 10.1007/s00432-003-0431-0

Google Scholar

[6] X.‏ Wang,‏ L. Yang, Z. Chen, M. Dong, Application of nanotechnology in cancer therapy and imaging. CA: Cancer. J. Clin. 58 (2008) 97-110.

Google Scholar

[7] E.E. Connor, J. Mwamuka, A. Gole, C.J. Murphy, M.D. Wyatt, Gold nanoparticles are taken up by human cells but do not cause acute cytotoxicity. Small. 1 (2005) 325-327.

DOI: 10.1002/smll.200400093

Google Scholar

[8] M.C. Daniel, D. Astruc, Gold nanoparticles: assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology. Chem. Rev. 104 (2004) 293-346.

DOI: 10.1021/cr030698+

Google Scholar

[9] D.C. Julien, S. Behnke, G. Wang, G.K. Murdoch, R.A. Hill, Utilization of monoclonal antibody-targeted nanomaterials in the treatment of cancer. MAbs. 3 (2011) 467-478.

DOI: 10.4161/mabs.3.5.16089

Google Scholar

[10] R. Singh, H.S. Nalwa, Medical applications of nanoparticles in biological imaging, cell labeling, antimicrobial agents, and anticancer nanodrugs. J. Biomed. Nanotechnol. 7 (2011) 489-503.

DOI: 10.1166/jbn.2011.1324

Google Scholar

[11] L.A. Dykman, N.G. Khlebtsov, Gold nanoparticles in biology and medicine: recent advances and prospects. Acta. Naturae. 3 (2011) 34-55.

DOI: 10.32607/20758251-2011-3-2-34-55

Google Scholar

[12] L. You, B. He, K. Uematsu, Z. Xu, J. Mazieres, et al, Inhibition of Wnt-1 signaling induces apoptosis in beta-catenin-deficient mesothelioma cells. Cancer. Res.64 (2004) 3474-3478.

DOI: 10.1158/0008-5472.can-04-0115

Google Scholar

[13] B. He, L You, K. Uematsu, Z. Xu, A. Lee, M. Matsangou, A monoclonal antibody against Wnt-1 induces apoptosis in human cancer cells. Neoplasia. 6 (2004).7-14.

DOI: 10.1016/s1476-5586(04)80048-4

Google Scholar

[14] S.K. Sivaraman, S. Kumar, V. Santhanam, Monodisperse sub-10 nm gold nanoparticles by reversing the order of addition in Turkevich method--the role of chloroauric acid. J. Colloid. Interface. Sci. 361 (2011) 543-547.

DOI: 10.1016/j.jcis.2011.06.015

Google Scholar

[15] J. Turkevich, P.C. Stevenson, J. Hillier, A Study of the Nucleation and Growth Processes in the Synthesis of Colloidal Gold. Discussions of the Farady Society. 11 (1951). 55-75.

DOI: 10.1039/df9511100055

Google Scholar

[16] A. Sharma, Z. Matharu, G Sumana, P.R. Solanki, et al, Antibody immobilized cysteamine functionalized-gold nanoparticles for aflatoxin detection. thin solid films. 519 (2010) 1213-1218.

DOI: 10.1016/j.tsf.2010.08.071

Google Scholar

[17] M. Losurdo, P.C. Wu, T.H. Kim, G. Bruno, A.S. Brown, Cysteamine-based functionalization of InAs surfaces: revealing the critical role of oxide interactions in biasing attachment. Langmuir. 28 (2012) 1235-1245.

DOI: 10.1021/la203436r

Google Scholar

[18] G Arya, M Vandana, S Acharya, SK Sahoo. , Enhanced antiproliferative activity of Herceptin (HER2)-conjugated gemcitabine-loaded chitosan nanoparticle in pancreatic cancer therapy. Nanomedicine. 7 (2011). 859-870.

DOI: 10.1016/j.nano.2011.03.009

Google Scholar

[19] NE Vrana, N Builles, H Kocak, P Gulay, V. Justin, EDC/NHS cross-linked collagen foams as scaffolds for artificial corneal stroma. J. Biomater. Sci. Polym. Ed. 18 (2007) 1527-1545.

DOI: 10.1163/156856207794761961

Google Scholar

[20] B.D. Chithrani, A.A. Ghazani, W.C. Chan, Determining the size and shape dependence of gold nanoparticle uptake into mammalian cells. Nano. Lett. 6 (2006). 6(4) 662-668.

DOI: 10.1021/nl052396o

Google Scholar

[21] T. Mosmann, Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods.65 (1983). 55-63.

DOI: 10.1016/0022-1759(83)90303-4

Google Scholar

[22] S Greenland, S.J. Senn, K.J. Rothman, J.B. Carlin, et al, Statistical tests, P values, confidence intervals, and power: a guide to misinterpretations. Eur. J. Epidemiol.31 (2016). 337-350.

DOI: 10.1007/s10654-016-0149-3

Google Scholar