Delivery Capacity and Anticancer Ability of the Berberine-Loaded Gold Nanoparticles to Promote the Apoptosis Effect in Breast Cancer
Gold nanoparticles (AuNPs) were fabricated with biocompatible collagen (Col) and then conjugated with berberine (BB), denoted as Au-Col-BB, to investigate the endocytic mechanisms in Her-2 breast cancer cell line and in bovine aortic endothelial cells (BAEC). Owing to the superior biocompatibility,...
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Veröffentlicht in: | Cancers 2021-10, Vol.13 (21), p.5317 |
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creator | Chiu, Chen-Feng Fu, Ru-Huei Hsu, Shan-hui Yu, Yang-Hao (Alex) Yang, Shun-Fa Tsao, Thomas Chang-Yao Chang, Kai-Bo Yeh, Chun-An Tang, Cheng-Ming Huang, Sheng-Chu Hung, Huey-Shan |
description | Gold nanoparticles (AuNPs) were fabricated with biocompatible collagen (Col) and then conjugated with berberine (BB), denoted as Au-Col-BB, to investigate the endocytic mechanisms in Her-2 breast cancer cell line and in bovine aortic endothelial cells (BAEC). Owing to the superior biocompatibility, tunable physicochemical properties, and potential functionalization with biomolecules, AuNPs have been well studied as carriers of biomolecules for diseases and cancer therapeutics. Composites of AuNPs with biopolymer, such as fibronectin or Col, have been revealed to increase cell proliferation, migration, and differentiation. BB is a natural compound with impressive health benefits, such as lowering blood sugar and reducing weight. In addition, BB can inhibit cell proliferation by modulating cell cycle progress and autophagy, and induce cell apoptosis in vivo and in vitro. In the current research, BB was conjugated on the Col-AuNP composite (“Au-Col”). The UV-Visible spectroscopy and infrared spectroscopy confirmed the conjugation of BB on Au-Col. The particle size of the Au-Col-BB conjugate was about 227 nm, determined by dynamic light scattering. Furthermore, Au-Col-BB was less cytotoxic to BAEC vs. Her-2 cell line in terms of MTT assay and cell cycle behavior. Au-Col-BB, compared to Au-Col, showed greater cell uptake capacity and potential cellular transportation by BAEC and Her-2 using the fluorescence-conjugated Au-Col-BB. In addition, the clathrin-mediated endocytosis and cell autophagy seemed to be the favorite endocytic mechanism for the internalization of Au-Col-BB by BAEC and Her-2. Au-Col-BB significantly inhibited cell migration in Her-2, but not in BAEC. Moreover, apoptotic cascade proteins, such as Bax and p21, were expressed in Her-2 after the treatment of Au-Col-BB. The tumor suppression was examined in a model of xenograft mice treated with Au-Col-BB nanovehicles. Results demonstrated that the tumor weight was remarkably reduced by the treatment of Au-Col-BB. Altogether, the promising findings of Au-Col-BB nanocarrier on Her-2 breast cancer cell line suggest that Au-Col-BB may be a good candidate of anticancer drug for the treatment of human breast cancer. |
doi_str_mv | 10.3390/cancers13215317 |
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Owing to the superior biocompatibility, tunable physicochemical properties, and potential functionalization with biomolecules, AuNPs have been well studied as carriers of biomolecules for diseases and cancer therapeutics. Composites of AuNPs with biopolymer, such as fibronectin or Col, have been revealed to increase cell proliferation, migration, and differentiation. BB is a natural compound with impressive health benefits, such as lowering blood sugar and reducing weight. In addition, BB can inhibit cell proliferation by modulating cell cycle progress and autophagy, and induce cell apoptosis in vivo and in vitro. In the current research, BB was conjugated on the Col-AuNP composite (“Au-Col”). The UV-Visible spectroscopy and infrared spectroscopy confirmed the conjugation of BB on Au-Col. The particle size of the Au-Col-BB conjugate was about 227 nm, determined by dynamic light scattering. Furthermore, Au-Col-BB was less cytotoxic to BAEC vs. Her-2 cell line in terms of MTT assay and cell cycle behavior. Au-Col-BB, compared to Au-Col, showed greater cell uptake capacity and potential cellular transportation by BAEC and Her-2 using the fluorescence-conjugated Au-Col-BB. In addition, the clathrin-mediated endocytosis and cell autophagy seemed to be the favorite endocytic mechanism for the internalization of Au-Col-BB by BAEC and Her-2. Au-Col-BB significantly inhibited cell migration in Her-2, but not in BAEC. Moreover, apoptotic cascade proteins, such as Bax and p21, were expressed in Her-2 after the treatment of Au-Col-BB. The tumor suppression was examined in a model of xenograft mice treated with Au-Col-BB nanovehicles. Results demonstrated that the tumor weight was remarkably reduced by the treatment of Au-Col-BB. Altogether, the promising findings of Au-Col-BB nanocarrier on Her-2 breast cancer cell line suggest that Au-Col-BB may be a good candidate of anticancer drug for the treatment of human breast cancer.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13215317</identifier><identifier>PMID: 34771481</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antitumor agents ; Aorta ; Apoptosis ; Autophagy ; Bax protein ; Berberine ; Biocompatibility ; Biopolymers ; Breast cancer ; Cancer therapies ; Cell cycle ; Cell differentiation ; Cell growth ; Cell migration ; Cell proliferation ; Chemokines ; Chemotherapy ; Clathrin ; Collagen ; Cytotoxicity ; Drug delivery systems ; Drugs ; Endocytosis ; Endothelial cells ; Epidermal growth factor ; ErbB-2 protein ; Fibronectin ; Fourier transforms ; Gold ; Internalization ; Investigations ; Kinases ; Metastasis ; Nanocomposites ; Nanoparticles ; Permeability ; Phagocytosis ; Proteins ; Tumor cell lines ; Tumor suppression ; Tumors ; Xenografts</subject><ispartof>Cancers, 2021-10, Vol.13 (21), p.5317</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-4b692e5a49ba5d5ff62026e9c74ca390a241916407aff1e9016a07b7c8119a9d3</citedby><cites>FETCH-LOGICAL-c398t-4b692e5a49ba5d5ff62026e9c74ca390a241916407aff1e9016a07b7c8119a9d3</cites><orcidid>0000-0003-2103-6670 ; 0000-0003-3399-055X ; 0000-0001-9367-1759 ; 0000-0002-0365-7927</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582582/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582582/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Chiu, Chen-Feng</creatorcontrib><creatorcontrib>Fu, Ru-Huei</creatorcontrib><creatorcontrib>Hsu, Shan-hui</creatorcontrib><creatorcontrib>Yu, Yang-Hao (Alex)</creatorcontrib><creatorcontrib>Yang, Shun-Fa</creatorcontrib><creatorcontrib>Tsao, Thomas Chang-Yao</creatorcontrib><creatorcontrib>Chang, Kai-Bo</creatorcontrib><creatorcontrib>Yeh, Chun-An</creatorcontrib><creatorcontrib>Tang, Cheng-Ming</creatorcontrib><creatorcontrib>Huang, Sheng-Chu</creatorcontrib><creatorcontrib>Hung, Huey-Shan</creatorcontrib><title>Delivery Capacity and Anticancer Ability of the Berberine-Loaded Gold Nanoparticles to Promote the Apoptosis Effect in Breast Cancer</title><title>Cancers</title><description>Gold nanoparticles (AuNPs) were fabricated with biocompatible collagen (Col) and then conjugated with berberine (BB), denoted as Au-Col-BB, to investigate the endocytic mechanisms in Her-2 breast cancer cell line and in bovine aortic endothelial cells (BAEC). Owing to the superior biocompatibility, tunable physicochemical properties, and potential functionalization with biomolecules, AuNPs have been well studied as carriers of biomolecules for diseases and cancer therapeutics. Composites of AuNPs with biopolymer, such as fibronectin or Col, have been revealed to increase cell proliferation, migration, and differentiation. BB is a natural compound with impressive health benefits, such as lowering blood sugar and reducing weight. In addition, BB can inhibit cell proliferation by modulating cell cycle progress and autophagy, and induce cell apoptosis in vivo and in vitro. In the current research, BB was conjugated on the Col-AuNP composite (“Au-Col”). The UV-Visible spectroscopy and infrared spectroscopy confirmed the conjugation of BB on Au-Col. The particle size of the Au-Col-BB conjugate was about 227 nm, determined by dynamic light scattering. Furthermore, Au-Col-BB was less cytotoxic to BAEC vs. Her-2 cell line in terms of MTT assay and cell cycle behavior. Au-Col-BB, compared to Au-Col, showed greater cell uptake capacity and potential cellular transportation by BAEC and Her-2 using the fluorescence-conjugated Au-Col-BB. In addition, the clathrin-mediated endocytosis and cell autophagy seemed to be the favorite endocytic mechanism for the internalization of Au-Col-BB by BAEC and Her-2. Au-Col-BB significantly inhibited cell migration in Her-2, but not in BAEC. Moreover, apoptotic cascade proteins, such as Bax and p21, were expressed in Her-2 after the treatment of Au-Col-BB. The tumor suppression was examined in a model of xenograft mice treated with Au-Col-BB nanovehicles. Results demonstrated that the tumor weight was remarkably reduced by the treatment of Au-Col-BB. Altogether, the promising findings of Au-Col-BB nanocarrier on Her-2 breast cancer cell line suggest that Au-Col-BB may be a good candidate of anticancer drug for the treatment of human breast cancer.</description><subject>Antitumor agents</subject><subject>Aorta</subject><subject>Apoptosis</subject><subject>Autophagy</subject><subject>Bax protein</subject><subject>Berberine</subject><subject>Biocompatibility</subject><subject>Biopolymers</subject><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Cell differentiation</subject><subject>Cell growth</subject><subject>Cell migration</subject><subject>Cell proliferation</subject><subject>Chemokines</subject><subject>Chemotherapy</subject><subject>Clathrin</subject><subject>Collagen</subject><subject>Cytotoxicity</subject><subject>Drug delivery systems</subject><subject>Drugs</subject><subject>Endocytosis</subject><subject>Endothelial cells</subject><subject>Epidermal growth factor</subject><subject>ErbB-2 protein</subject><subject>Fibronectin</subject><subject>Fourier transforms</subject><subject>Gold</subject><subject>Internalization</subject><subject>Investigations</subject><subject>Kinases</subject><subject>Metastasis</subject><subject>Nanocomposites</subject><subject>Nanoparticles</subject><subject>Permeability</subject><subject>Phagocytosis</subject><subject>Proteins</subject><subject>Tumor cell lines</subject><subject>Tumor 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Berberine-Loaded Gold Nanoparticles to Promote the Apoptosis Effect in Breast Cancer</title><author>Chiu, Chen-Feng ; Fu, Ru-Huei ; Hsu, Shan-hui ; Yu, Yang-Hao (Alex) ; Yang, Shun-Fa ; Tsao, Thomas Chang-Yao ; Chang, Kai-Bo ; Yeh, Chun-An ; Tang, Cheng-Ming ; Huang, Sheng-Chu ; Hung, Huey-Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-4b692e5a49ba5d5ff62026e9c74ca390a241916407aff1e9016a07b7c8119a9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antitumor agents</topic><topic>Aorta</topic><topic>Apoptosis</topic><topic>Autophagy</topic><topic>Bax protein</topic><topic>Berberine</topic><topic>Biocompatibility</topic><topic>Biopolymers</topic><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Cell cycle</topic><topic>Cell differentiation</topic><topic>Cell growth</topic><topic>Cell migration</topic><topic>Cell proliferation</topic><topic>Chemokines</topic><topic>Chemotherapy</topic><topic>Clathrin</topic><topic>Collagen</topic><topic>Cytotoxicity</topic><topic>Drug delivery systems</topic><topic>Drugs</topic><topic>Endocytosis</topic><topic>Endothelial cells</topic><topic>Epidermal growth factor</topic><topic>ErbB-2 protein</topic><topic>Fibronectin</topic><topic>Fourier transforms</topic><topic>Gold</topic><topic>Internalization</topic><topic>Investigations</topic><topic>Kinases</topic><topic>Metastasis</topic><topic>Nanocomposites</topic><topic>Nanoparticles</topic><topic>Permeability</topic><topic>Phagocytosis</topic><topic>Proteins</topic><topic>Tumor cell lines</topic><topic>Tumor suppression</topic><topic>Tumors</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiu, Chen-Feng</creatorcontrib><creatorcontrib>Fu, Ru-Huei</creatorcontrib><creatorcontrib>Hsu, Shan-hui</creatorcontrib><creatorcontrib>Yu, Yang-Hao 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conjugated with berberine (BB), denoted as Au-Col-BB, to investigate the endocytic mechanisms in Her-2 breast cancer cell line and in bovine aortic endothelial cells (BAEC). Owing to the superior biocompatibility, tunable physicochemical properties, and potential functionalization with biomolecules, AuNPs have been well studied as carriers of biomolecules for diseases and cancer therapeutics. Composites of AuNPs with biopolymer, such as fibronectin or Col, have been revealed to increase cell proliferation, migration, and differentiation. BB is a natural compound with impressive health benefits, such as lowering blood sugar and reducing weight. In addition, BB can inhibit cell proliferation by modulating cell cycle progress and autophagy, and induce cell apoptosis in vivo and in vitro. In the current research, BB was conjugated on the Col-AuNP composite (“Au-Col”). The UV-Visible spectroscopy and infrared spectroscopy confirmed the conjugation of BB on Au-Col. The particle size of the Au-Col-BB conjugate was about 227 nm, determined by dynamic light scattering. Furthermore, Au-Col-BB was less cytotoxic to BAEC vs. Her-2 cell line in terms of MTT assay and cell cycle behavior. Au-Col-BB, compared to Au-Col, showed greater cell uptake capacity and potential cellular transportation by BAEC and Her-2 using the fluorescence-conjugated Au-Col-BB. In addition, the clathrin-mediated endocytosis and cell autophagy seemed to be the favorite endocytic mechanism for the internalization of Au-Col-BB by BAEC and Her-2. Au-Col-BB significantly inhibited cell migration in Her-2, but not in BAEC. Moreover, apoptotic cascade proteins, such as Bax and p21, were expressed in Her-2 after the treatment of Au-Col-BB. The tumor suppression was examined in a model of xenograft mice treated with Au-Col-BB nanovehicles. Results demonstrated that the tumor weight was remarkably reduced by the treatment of Au-Col-BB. Altogether, the promising findings of Au-Col-BB nanocarrier on Her-2 breast cancer cell line suggest that Au-Col-BB may be a good candidate of anticancer drug for the treatment of human breast cancer.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34771481</pmid><doi>10.3390/cancers13215317</doi><orcidid>https://orcid.org/0000-0003-2103-6670</orcidid><orcidid>https://orcid.org/0000-0003-3399-055X</orcidid><orcidid>https://orcid.org/0000-0001-9367-1759</orcidid><orcidid>https://orcid.org/0000-0002-0365-7927</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antitumor agents Aorta Apoptosis Autophagy Bax protein Berberine Biocompatibility Biopolymers Breast cancer Cancer therapies Cell cycle Cell differentiation Cell growth Cell migration Cell proliferation Chemokines Chemotherapy Clathrin Collagen Cytotoxicity Drug delivery systems Drugs Endocytosis Endothelial cells Epidermal growth factor ErbB-2 protein Fibronectin Fourier transforms Gold Internalization Investigations Kinases Metastasis Nanocomposites Nanoparticles Permeability Phagocytosis Proteins Tumor cell lines Tumor suppression Tumors Xenografts |
title | Delivery Capacity and Anticancer Ability of the Berberine-Loaded Gold Nanoparticles to Promote the Apoptosis Effect in Breast Cancer |
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