Doxorubicin Conjugated to Glutathione Stabilized Gold Nanoparticles (Au-GSH-Dox) as an Effective Therapeutic Agent for Feline Injection-Site Sarcomas-Chick Embryo Chorioallantoic Membrane Study
Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site sarcomas includes radical surgery, radiotherapy and/or chemotherapy. In our previous study it has been demonstrated that doxorubicin conjugated...
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Published in | Molecules (Basel, Switzerland) Vol. 22; no. 2; p. 253 |
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Abstract | Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site sarcomas includes radical surgery, radiotherapy and/or chemotherapy. In our previous study it has been demonstrated that doxorubicin conjugated to glutathione-stabilized gold nanoparticles (Au-GSH-Dox) has higher cytotoxic effects than free doxorubicin for feline fibrosarcoma cell lines with high glycoprotein P activity (FFS1, FFS3). The aim of the present study was to assess the effectiveness of intratumoural injection of Au-GSH-Dox on the growth of tumours from the FFS1 and FFS3 cell lines on chick embryo chorioallantoic membrane. This model has been utilized both in human and veterinary medicine for preclinical oncological studies. The influence of intratumoural injections of Au-GSH-Dox, glutathione-stabilized gold nanoparticles and doxorubicin alone on the Ki-67 proliferation marker was also checked. We demonstrated that the volume ratio of tumours from the FFS1 and FFS3 cell lines was significantly (
< 0.01) decreased after a single intratumoural injection of Au-GSH-Dox, which confirms the positive results of in vitro studies and indicates that Au-GSH-Dox may be a potent new therapeutic agent for feline injection-site sarcomas. |
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AbstractList | Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site sarcomas includes radical surgery, radiotherapy and/or chemotherapy. In our previous study it has been demonstrated that doxorubicin conjugated to glutathione-stabilized gold nanoparticles (Au-GSH-Dox) has higher cytotoxic effects than free doxorubicin for feline fibrosarcoma cell lines with high glycoprotein P activity (FFS1, FFS3). The aim of the present study was to assess the effectiveness of intratumoural injection of Au-GSH-Dox on the growth of tumours from the FFS1 and FFS3 cell lines on chick embryo chorioallantoic membrane. This model has been utilized both in human and veterinary medicine for preclinical oncological studies. The influence of intratumoural injections of Au-GSH-Dox, glutathione-stabilized gold nanoparticles and doxorubicin alone on the Ki-67 proliferation marker was also checked. We demonstrated that the volume ratio of tumours from the FFS1 and FFS3 cell lines was significantly (p < 0.01) decreased after a single intratumoural injection of Au-GSH-Dox, which confirms the positive results of in vitro studies and indicates that Au-GSH-Dox may be a potent new therapeutic agent for feline injection-site sarcomas. Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site sarcomas includes radical surgery, radiotherapy and/or chemotherapy. In our previous study it has been demonstrated that doxorubicin conjugated to glutathione-stabilized gold nanoparticles (Au-GSH-Dox) has higher cytotoxic effects than free doxorubicin for feline fibrosarcoma cell lines with high glycoprotein P activity (FFS1, FFS3). The aim of the present study was to assess the effectiveness of intratumoural injection of Au-GSH-Dox on the growth of tumours from the FFS1 and FFS3 cell lines on chick embryo chorioallantoic membrane. This model has been utilized both in human and veterinary medicine for preclinical oncological studies. The influence of intratumoural injections of Au-GSH-Dox, glutathione-stabilized gold nanoparticles and doxorubicin alone on the Ki-67 proliferation marker was also checked. We demonstrated that the volume ratio of tumours from the FFS1 and FFS3 cell lines was significantly ( p < 0.01) decreased after a single intratumoural injection of Au-GSH-Dox, which confirms the positive results of in vitro studies and indicates that Au-GSH-Dox may be a potent new therapeutic agent for feline injection-site sarcomas. Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site sarcomas includes radical surgery, radiotherapy and/or chemotherapy. In our previous study it has been demonstrated that doxorubicin conjugated to glutathione-stabilized gold nanoparticles (Au-GSH-Dox) has higher cytotoxic effects than free doxorubicin for feline fibrosarcoma cell lines with high glycoprotein P activity (FFS1, FFS3). The aim of the present study was to assess the effectiveness of intratumoural injection of Au-GSH-Dox on the growth of tumours from the FFS1 and FFS3 cell lines on chick embryo chorioallantoic membrane. This model has been utilized both in human and veterinary medicine for preclinical oncological studies. The influence of intratumoural injections of Au-GSH-Dox, glutathione-stabilized gold nanoparticles and doxorubicin alone on the Ki-67 proliferation marker was also checked. We demonstrated that the volume ratio of tumours from the FFS1 and FFS3 cell lines was significantly (p < 0.01) decreased after a single intratumoural injection of Au-GSH-Dox, which confirms the positive results of in vitro studies and indicates that Au-GSH-Dox may be a potent new therapeutic agent for feline injection-site sarcomas. Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site sarcomas includes radical surgery, radiotherapy and/or chemotherapy. In our previous study it has been demonstrated that doxorubicin conjugated to glutathione-stabilized gold nanoparticles (Au-GSH-Dox) has higher cytotoxic effects than free doxorubicin for feline fibrosarcoma cell lines with high glycoprotein P activity (FFS1, FFS3). The aim of the present study was to assess the effectiveness of intratumoural injection of Au-GSH-Dox on the growth of tumours from the FFS1 and FFS3 cell lines on chick embryo chorioallantoic membrane. This model has been utilized both in human and veterinary medicine for preclinical oncological studies. The influence of intratumoural injections of Au-GSH-Dox, glutathione-stabilized gold nanoparticles and doxorubicin alone on the Ki-67 proliferation marker was also checked. We demonstrated that the volume ratio of tumours from the FFS1 and FFS3 cell lines was significantly ( < 0.01) decreased after a single intratumoural injection of Au-GSH-Dox, which confirms the positive results of in vitro studies and indicates that Au-GSH-Dox may be a potent new therapeutic agent for feline injection-site sarcomas. |
Author | Żbikowski, Artur Lechowski, Roman Mieczkowski, Józef Wójcik, Michał Lewandowski, Wiktor Król, Magdalena Zabielska-Koczywąs, Katarzyna Dolka, Izabella |
AuthorAffiliation | 1 Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland; izabella_dolka@sggw.pl (I.D.); magdalena_krol@sggw.pl (M.K.); artur_zbikowski@sggw.pl (A.Ż.); roman_lechowski@sggw.pl (R.L.) 2 Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland; wlewandowski@chem.uw.edu.pl (W.L.); mieczkow@chem.uw.edu.pl (J.M.); mwojcik@chem.uw.edu.pl (M.W.) |
AuthorAffiliation_xml | – name: 1 Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland; izabella_dolka@sggw.pl (I.D.); magdalena_krol@sggw.pl (M.K.); artur_zbikowski@sggw.pl (A.Ż.); roman_lechowski@sggw.pl (R.L.) – name: 2 Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland; wlewandowski@chem.uw.edu.pl (W.L.); mieczkow@chem.uw.edu.pl (J.M.); mwojcik@chem.uw.edu.pl (M.W.) |
Author_xml | – sequence: 1 givenname: Katarzyna surname: Zabielska-Koczywąs fullname: Zabielska-Koczywąs, Katarzyna email: katarzyna_zabielska@sggw.pl organization: Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland. katarzyna_zabielska@sggw.pl – sequence: 2 givenname: Izabella surname: Dolka fullname: Dolka, Izabella email: izabella_dolka@sggw.pl organization: Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland. izabella_dolka@sggw.pl – sequence: 3 givenname: Magdalena surname: Król fullname: Król, Magdalena email: magdalena_krol@sggw.pl organization: Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland. magdalena_krol@sggw.pl – sequence: 4 givenname: Artur surname: Żbikowski fullname: Żbikowski, Artur email: artur_zbikowski@sggw.pl organization: Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland. artur_zbikowski@sggw.pl – sequence: 5 givenname: Wiktor surname: Lewandowski fullname: Lewandowski, Wiktor email: wlewandowski@chem.uw.edu.pl organization: Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland. wlewandowski@chem.uw.edu.pl – sequence: 6 givenname: Józef surname: Mieczkowski fullname: Mieczkowski, Józef email: mieczkow@chem.uw.edu.pl organization: Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland. mieczkow@chem.uw.edu.pl – sequence: 7 givenname: Michał surname: Wójcik fullname: Wójcik, Michał email: mwojcik@chem.uw.edu.pl organization: Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland. mwojcik@chem.uw.edu.pl – sequence: 8 givenname: Roman surname: Lechowski fullname: Lechowski, Roman email: roman_lechowski@sggw.pl organization: Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, 02-776 Warsaw, Poland. roman_lechowski@sggw.pl |
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Keywords | Ki-67 in vivo study doxorubicin CAM assay gold nanoparticles feline injection-site sarcoma |
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Snippet | Feline injection-site sarcomas are malignant skin tumours with a high local recurrence rate, ranging from 14% to 28%. The treatment of feline injection-site... |
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SubjectTerms | Animals Antibiotics, Antineoplastic - administration & dosage Biomarkers CAM assay Cats Cell Line, Tumor Cell lines Chemical compounds Chemotherapy Chick Embryo Chorioallantoic membrane Chorioallantoic Membrane - pathology Cytotoxicity Disease Models, Animal Doxorubicin Doxorubicin - administration & dosage Embryos feline injection-site sarcoma Fibrosarcoma Glutathione - chemistry Gold Gold - chemistry gold nanoparticles in vivo study Injection Injections, Intralesional Ki-67 Membranes Metal Nanoparticles - chemistry Nanoparticles Pharmacology Radiation therapy Sarcoma Sarcoma - drug therapy Sarcoma - metabolism Sarcoma - pathology Tumor Burden - drug effects Tumors Veterinary medicine |
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Title | Doxorubicin Conjugated to Glutathione Stabilized Gold Nanoparticles (Au-GSH-Dox) as an Effective Therapeutic Agent for Feline Injection-Site Sarcomas-Chick Embryo Chorioallantoic Membrane Study |
URI | https://www.ncbi.nlm.nih.gov/pubmed/28208720 https://www.proquest.com/docview/1878403297 https://search.proquest.com/docview/1869968322 https://search.proquest.com/docview/1881748506 https://pubmed.ncbi.nlm.nih.gov/PMC6155676 https://doaj.org/article/7043546ddb974052a1dac4a86f9cd10c |
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