author_facet Guney Eskiler, Gamze
Kani, Ibrahim
Guney Eskiler, Gamze
Kani, Ibrahim
author Guney Eskiler, Gamze
Kani, Ibrahim
spellingShingle Guney Eskiler, Gamze
Kani, Ibrahim
Turkish Journal of Biochemistry
In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
Biochemistry (medical)
Clinical Biochemistry
Molecular Biology
Biochemistry
author_sort guney eskiler, gamze
spelling Guney Eskiler, Gamze Kani, Ibrahim 1303-829X 0250-4685 Walter de Gruyter GmbH Biochemistry (medical) Clinical Biochemistry Molecular Biology Biochemistry http://dx.doi.org/10.1515/tjb-2019-0013 <jats:title>Abstract</jats:title> <jats:sec id="j_tjb-2019-0013_s_999_w2aab3b7c34b1b6b1aab1c15b1Aa"> <jats:title>Background</jats:title> <jats:p>The synthesis of new ligand and transition metal complexes have drawn great attention in cancer treatment due to excellent DNA cleavage activities and high antitumor activity.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_998_w2aab3b7c34b1b6b1aab1c15b2Aa"> <jats:title>Objective</jats:title> <jats:p>The purpose of this study was to synthesize a new Zn(II) complex with 2,2′-bipyridine (bpy) ligand, [Zn(bpy)<jats:sub>2</jats:sub>(H<jats:sub>2</jats:sub>O)]2(ClO<jats:sub>4</jats:sub>), and to investigate the potential therapeutic activity against breast cancer.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_997_w2aab3b7c34b1b6b1aab1c15b3Aa"> <jats:title>Materials and methods</jats:title> <jats:p>Zn(II) complex was obtained and structurally characterized using crystallography and other spectroscopic methods. The cytotoxic and apoptotic effects of Zn(II) complex on MCF7 breast cancer and HUVEC control cells were evaluated by WST-1, Annexin V and cell cycle analysis.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_996_w2aab3b7c34b1b6b1aab1c15b4Aa"> <jats:title>Results</jats:title> <jats:p>The spectroscopic data demonstrated that Zn(II) complex was successfully synthesized. Furthermore, Zn(II) complex exhibited significant cytotoxic effect on MCF7 breast cancer and HUVEC cells (p &lt; 0.01). MCF7 and HUVEC cells proliferation was reduced to 11.0% and 52.6%, respectively at 10 μM for 48 h. Additionally, Zn(II) complex significantly induced apoptotic cell death (84.87%) and caused S phase arrest (36.4%) in MCF7 cells at 10 μM (p &lt; 0.01).</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_995_w2aab3b7c34b1b6b1aab1c15b5Aa"> <jats:title>Conclusions</jats:title> <jats:p>Zn(II) complex has great therapeutic potential for the treatment of breast cancer. However, further studies are warranted to identify the underlying mechanisms of apoptotic cell death and to reduce the toxicity of Zn(II) complex on control cells.</jats:p> </jats:sec> <i>In vitro</i> apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells Turkish Journal of Biochemistry
doi_str_mv 10.1515/tjb-2019-0013
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Biologie
Chemie und Pharmazie
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recordtype ai
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series Turkish Journal of Biochemistry
source_id 49
title In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_unstemmed In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_full In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_fullStr In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_full_unstemmed In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_short In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_sort <i>in vitro</i> apoptotic effect of zinc(ii) complex with n-donor heterocyclic ligand on breast cancer cells
topic Biochemistry (medical)
Clinical Biochemistry
Molecular Biology
Biochemistry
url http://dx.doi.org/10.1515/tjb-2019-0013
publishDate 2019
physical 761-768
description <jats:title>Abstract</jats:title> <jats:sec id="j_tjb-2019-0013_s_999_w2aab3b7c34b1b6b1aab1c15b1Aa"> <jats:title>Background</jats:title> <jats:p>The synthesis of new ligand and transition metal complexes have drawn great attention in cancer treatment due to excellent DNA cleavage activities and high antitumor activity.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_998_w2aab3b7c34b1b6b1aab1c15b2Aa"> <jats:title>Objective</jats:title> <jats:p>The purpose of this study was to synthesize a new Zn(II) complex with 2,2′-bipyridine (bpy) ligand, [Zn(bpy)<jats:sub>2</jats:sub>(H<jats:sub>2</jats:sub>O)]2(ClO<jats:sub>4</jats:sub>), and to investigate the potential therapeutic activity against breast cancer.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_997_w2aab3b7c34b1b6b1aab1c15b3Aa"> <jats:title>Materials and methods</jats:title> <jats:p>Zn(II) complex was obtained and structurally characterized using crystallography and other spectroscopic methods. The cytotoxic and apoptotic effects of Zn(II) complex on MCF7 breast cancer and HUVEC control cells were evaluated by WST-1, Annexin V and cell cycle analysis.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_996_w2aab3b7c34b1b6b1aab1c15b4Aa"> <jats:title>Results</jats:title> <jats:p>The spectroscopic data demonstrated that Zn(II) complex was successfully synthesized. Furthermore, Zn(II) complex exhibited significant cytotoxic effect on MCF7 breast cancer and HUVEC cells (p &lt; 0.01). MCF7 and HUVEC cells proliferation was reduced to 11.0% and 52.6%, respectively at 10 μM for 48 h. Additionally, Zn(II) complex significantly induced apoptotic cell death (84.87%) and caused S phase arrest (36.4%) in MCF7 cells at 10 μM (p &lt; 0.01).</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_995_w2aab3b7c34b1b6b1aab1c15b5Aa"> <jats:title>Conclusions</jats:title> <jats:p>Zn(II) complex has great therapeutic potential for the treatment of breast cancer. However, further studies are warranted to identify the underlying mechanisms of apoptotic cell death and to reduce the toxicity of Zn(II) complex on control cells.</jats:p> </jats:sec>
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author Guney Eskiler, Gamze, Kani, Ibrahim
author_facet Guney Eskiler, Gamze, Kani, Ibrahim, Guney Eskiler, Gamze, Kani, Ibrahim
author_sort guney eskiler, gamze
container_issue 6
container_start_page 761
container_title Turkish Journal of Biochemistry
container_volume 44
description <jats:title>Abstract</jats:title> <jats:sec id="j_tjb-2019-0013_s_999_w2aab3b7c34b1b6b1aab1c15b1Aa"> <jats:title>Background</jats:title> <jats:p>The synthesis of new ligand and transition metal complexes have drawn great attention in cancer treatment due to excellent DNA cleavage activities and high antitumor activity.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_998_w2aab3b7c34b1b6b1aab1c15b2Aa"> <jats:title>Objective</jats:title> <jats:p>The purpose of this study was to synthesize a new Zn(II) complex with 2,2′-bipyridine (bpy) ligand, [Zn(bpy)<jats:sub>2</jats:sub>(H<jats:sub>2</jats:sub>O)]2(ClO<jats:sub>4</jats:sub>), and to investigate the potential therapeutic activity against breast cancer.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_997_w2aab3b7c34b1b6b1aab1c15b3Aa"> <jats:title>Materials and methods</jats:title> <jats:p>Zn(II) complex was obtained and structurally characterized using crystallography and other spectroscopic methods. The cytotoxic and apoptotic effects of Zn(II) complex on MCF7 breast cancer and HUVEC control cells were evaluated by WST-1, Annexin V and cell cycle analysis.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_996_w2aab3b7c34b1b6b1aab1c15b4Aa"> <jats:title>Results</jats:title> <jats:p>The spectroscopic data demonstrated that Zn(II) complex was successfully synthesized. Furthermore, Zn(II) complex exhibited significant cytotoxic effect on MCF7 breast cancer and HUVEC cells (p &lt; 0.01). MCF7 and HUVEC cells proliferation was reduced to 11.0% and 52.6%, respectively at 10 μM for 48 h. Additionally, Zn(II) complex significantly induced apoptotic cell death (84.87%) and caused S phase arrest (36.4%) in MCF7 cells at 10 μM (p &lt; 0.01).</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_995_w2aab3b7c34b1b6b1aab1c15b5Aa"> <jats:title>Conclusions</jats:title> <jats:p>Zn(II) complex has great therapeutic potential for the treatment of breast cancer. However, further studies are warranted to identify the underlying mechanisms of apoptotic cell death and to reduce the toxicity of Zn(II) complex on control cells.</jats:p> </jats:sec>
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id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTUxNS90amItMjAxOS0wMDEz
imprint Walter de Gruyter GmbH, 2019
imprint_str_mv Walter de Gruyter GmbH, 2019
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spelling Guney Eskiler, Gamze Kani, Ibrahim 1303-829X 0250-4685 Walter de Gruyter GmbH Biochemistry (medical) Clinical Biochemistry Molecular Biology Biochemistry http://dx.doi.org/10.1515/tjb-2019-0013 <jats:title>Abstract</jats:title> <jats:sec id="j_tjb-2019-0013_s_999_w2aab3b7c34b1b6b1aab1c15b1Aa"> <jats:title>Background</jats:title> <jats:p>The synthesis of new ligand and transition metal complexes have drawn great attention in cancer treatment due to excellent DNA cleavage activities and high antitumor activity.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_998_w2aab3b7c34b1b6b1aab1c15b2Aa"> <jats:title>Objective</jats:title> <jats:p>The purpose of this study was to synthesize a new Zn(II) complex with 2,2′-bipyridine (bpy) ligand, [Zn(bpy)<jats:sub>2</jats:sub>(H<jats:sub>2</jats:sub>O)]2(ClO<jats:sub>4</jats:sub>), and to investigate the potential therapeutic activity against breast cancer.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_997_w2aab3b7c34b1b6b1aab1c15b3Aa"> <jats:title>Materials and methods</jats:title> <jats:p>Zn(II) complex was obtained and structurally characterized using crystallography and other spectroscopic methods. The cytotoxic and apoptotic effects of Zn(II) complex on MCF7 breast cancer and HUVEC control cells were evaluated by WST-1, Annexin V and cell cycle analysis.</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_996_w2aab3b7c34b1b6b1aab1c15b4Aa"> <jats:title>Results</jats:title> <jats:p>The spectroscopic data demonstrated that Zn(II) complex was successfully synthesized. Furthermore, Zn(II) complex exhibited significant cytotoxic effect on MCF7 breast cancer and HUVEC cells (p &lt; 0.01). MCF7 and HUVEC cells proliferation was reduced to 11.0% and 52.6%, respectively at 10 μM for 48 h. Additionally, Zn(II) complex significantly induced apoptotic cell death (84.87%) and caused S phase arrest (36.4%) in MCF7 cells at 10 μM (p &lt; 0.01).</jats:p> </jats:sec> <jats:sec id="j_tjb-2019-0013_s_995_w2aab3b7c34b1b6b1aab1c15b5Aa"> <jats:title>Conclusions</jats:title> <jats:p>Zn(II) complex has great therapeutic potential for the treatment of breast cancer. However, further studies are warranted to identify the underlying mechanisms of apoptotic cell death and to reduce the toxicity of Zn(II) complex on control cells.</jats:p> </jats:sec> <i>In vitro</i> apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells Turkish Journal of Biochemistry
spellingShingle Guney Eskiler, Gamze, Kani, Ibrahim, Turkish Journal of Biochemistry, In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells, Biochemistry (medical), Clinical Biochemistry, Molecular Biology, Biochemistry
title In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_full In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_fullStr In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_full_unstemmed In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_short In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
title_sort <i>in vitro</i> apoptotic effect of zinc(ii) complex with n-donor heterocyclic ligand on breast cancer cells
title_unstemmed In vitro apoptotic effect of Zinc(II) complex with N-donor heterocyclic ligand on breast cancer cells
topic Biochemistry (medical), Clinical Biochemistry, Molecular Biology, Biochemistry
url http://dx.doi.org/10.1515/tjb-2019-0013