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,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancers 2021-10, Vol.13 (21), p.5317
Hauptverfasser: 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
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 21
container_start_page 5317
container_title Cancers
container_volume 13
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
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8582582</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2597495977</sourcerecordid><originalsourceid>FETCH-LOGICAL-c398t-4b692e5a49ba5d5ff62026e9c74ca390a241916407aff1e9016a07b7c8119a9d3</originalsourceid><addsrcrecordid>eNpdkU1vFDEMhkcIRKvSM9dIXLgMzddMJhek7fYDpBVwgHPkyTg01WwyJNlKe-eHN8tWCGpFTuQ8fh3HTfOW0Q9CaHphIVhMmQnOOsHUi-aUU8Xbvtfy5T_nk-Y853taTVSqV6-bEyGVYnJgp83vK5z9A6Y9WcMC1pc9gTCRVSj-KE9Wo58P4ehIuUNyiWnE5AO2mwgTTuQ2zhP5AiEukGrSjJmUSL6luI0F_6SslriUmH0m186hLcQHcpkQcqlFDzXeNK8czBnPn_az5sfN9ff1p3bz9fbzerVprdBDaeXYa44dSD1CN3XO9ZzyHrVV0kL9EOCSadZLqsA5hpqyHqgalR0Y06AncdZ8POouu3GLk8VQEsxmSX4LaW8iePP_TfB35md8MEM38LqqwPsngRR_7TAXs_XZ4jxDwLjLhndaSV2dqui7Z-h93KVQ2ztQPWV0GFilLo6UTTHnhO7vYxg1hyGbZ0MWj6T9m04</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2596010881</pqid></control><display><type>article</type><title>Delivery Capacity and Anticancer Ability of the Berberine-Loaded Gold Nanoparticles to Promote the Apoptosis Effect in Breast Cancer</title><source>PubMed Central Open Access</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 suppression</subject><subject>Tumors</subject><subject>Xenografts</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU1vFDEMhkcIRKvSM9dIXLgMzddMJhek7fYDpBVwgHPkyTg01WwyJNlKe-eHN8tWCGpFTuQ8fh3HTfOW0Q9CaHphIVhMmQnOOsHUi-aUU8Xbvtfy5T_nk-Y853taTVSqV6-bEyGVYnJgp83vK5z9A6Y9WcMC1pc9gTCRVSj-KE9Wo58P4ehIuUNyiWnE5AO2mwgTTuQ2zhP5AiEukGrSjJmUSL6luI0F_6SslriUmH0m186hLcQHcpkQcqlFDzXeNK8czBnPn_az5sfN9ff1p3bz9fbzerVprdBDaeXYa44dSD1CN3XO9ZzyHrVV0kL9EOCSadZLqsA5hpqyHqgalR0Y06AncdZ8POouu3GLk8VQEsxmSX4LaW8iePP_TfB35md8MEM38LqqwPsngRR_7TAXs_XZ4jxDwLjLhndaSV2dqui7Z-h93KVQ2ztQPWV0GFilLo6UTTHnhO7vYxg1hyGbZ0MWj6T9m04</recordid><startdate>20211022</startdate><enddate>20211022</enddate><creator>Chiu, Chen-Feng</creator><creator>Fu, Ru-Huei</creator><creator>Hsu, Shan-hui</creator><creator>Yu, Yang-Hao (Alex)</creator><creator>Yang, Shun-Fa</creator><creator>Tsao, Thomas Chang-Yao</creator><creator>Chang, Kai-Bo</creator><creator>Yeh, Chun-An</creator><creator>Tang, Cheng-Ming</creator><creator>Huang, Sheng-Chu</creator><creator>Hung, Huey-Shan</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><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></search><sort><creationdate>20211022</creationdate><title>Delivery Capacity and Anticancer Ability of the 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 (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><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiu, Chen-Feng</au><au>Fu, Ru-Huei</au><au>Hsu, Shan-hui</au><au>Yu, Yang-Hao (Alex)</au><au>Yang, Shun-Fa</au><au>Tsao, Thomas Chang-Yao</au><au>Chang, Kai-Bo</au><au>Yeh, Chun-An</au><au>Tang, Cheng-Ming</au><au>Huang, Sheng-Chu</au><au>Hung, Huey-Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Delivery Capacity and Anticancer Ability of the Berberine-Loaded Gold Nanoparticles to Promote the Apoptosis Effect in Breast Cancer</atitle><jtitle>Cancers</jtitle><date>2021-10-22</date><risdate>2021</risdate><volume>13</volume><issue>21</issue><spage>5317</spage><pages>5317-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>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.</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>
fulltext fulltext
identifier ISSN: 2072-6694
ispartof Cancers, 2021-10, Vol.13 (21), p.5317
issn 2072-6694
2072-6694
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8582582
source PubMed Central Open Access; MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T15%3A10%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Delivery%20Capacity%20and%20Anticancer%20Ability%20of%20the%20Berberine-Loaded%20Gold%20Nanoparticles%20to%20Promote%20the%20Apoptosis%20Effect%20in%20Breast%20Cancer&rft.jtitle=Cancers&rft.au=Chiu,%20Chen-Feng&rft.date=2021-10-22&rft.volume=13&rft.issue=21&rft.spage=5317&rft.pages=5317-&rft.issn=2072-6694&rft.eissn=2072-6694&rft_id=info:doi/10.3390/cancers13215317&rft_dat=%3Cproquest_pubme%3E2597495977%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2596010881&rft_id=info:pmid/34771481&rfr_iscdi=true