ROS-mediated lipid peroxidation as a result of Cu() interaction with FomA protein fragments of : relevance to colorectal carcinogenesis
The ability of the studied FomA protein fragments of Fusobacterium nucleatum ( Fn ) with copper( ii ) ions (Cu( ii )-Ac-KGHGNGEEGTPTVHNE-NH 2 ( 1Cu ) and its cyclic analogue Cu( ii )-cyclo(KGHGNGEEGTPTVHNE) ( 2Cu )) to induce reactive oxygen species (ROS) generation, as a result of red-ox processes,...
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Veröffentlicht in: | Metallomics 2019-12, Vol.11 (12), p.266-277 |
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creator | Lesiów, Monika Katarzyna Komarnicka, Urszula Katarzyna Kyzio, Agnieszka Bie ko, Alina Pietrzyk, Piotr |
description | The ability of the studied FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) with copper(
ii
) ions (Cu(
ii
)-Ac-KGHGNGEEGTPTVHNE-NH
2
(
1Cu
) and its cyclic analogue Cu(
ii
)-cyclo(KGHGNGEEGTPTVHNE) (
2Cu
)) to induce reactive oxygen species (ROS) generation, as a result of red-ox processes, was determined by UV-Vis, luminescence methods, spin trapping and cyclic voltamperometry. The contribution of
1
O
2
and &z.rad;OH to DNA degradation was proved using gel electrophoresis. Furthermore, the pronounced generation of ROS by mouse colon carcinoma cells (CT26) stimulated by both copper(
ii
) complexes was confirmed. A fluorescence method allowed the total amounts of ROS generated inside the CT26 cells to be detected, while the spin trapping technique proved that free radicals mainly attached to the membrane surface. These last results are in agreement with the data obtained from the ICP-MS method, which demonstrates that
1Cu
and
2Cu
complexes are not efficiently accumulated inside the cell. Furthermore, the role of ROS in lipid peroxidation was established. The above-mentioned factors may clearly indicate the contribution of ROS generated by the studied copper(
ii
) complexes to colonic cell damage, which can lead to a carcinogenesis process. This study may be an important step to recognize and understand the mechanism of colon cancer initiation.
The ability of Cu(
ii
) complexes with FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) to produce reactive oxygen species (ROS) was determined. |
doi_str_mv | 10.1039/c9mt00179d |
format | Article |
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Fusobacterium nucleatum
(
Fn
) with copper(
ii
) ions (Cu(
ii
)-Ac-KGHGNGEEGTPTVHNE-NH
2
(
1Cu
) and its cyclic analogue Cu(
ii
)-cyclo(KGHGNGEEGTPTVHNE) (
2Cu
)) to induce reactive oxygen species (ROS) generation, as a result of red-ox processes, was determined by UV-Vis, luminescence methods, spin trapping and cyclic voltamperometry. The contribution of
1
O
2
and &z.rad;OH to DNA degradation was proved using gel electrophoresis. Furthermore, the pronounced generation of ROS by mouse colon carcinoma cells (CT26) stimulated by both copper(
ii
) complexes was confirmed. A fluorescence method allowed the total amounts of ROS generated inside the CT26 cells to be detected, while the spin trapping technique proved that free radicals mainly attached to the membrane surface. These last results are in agreement with the data obtained from the ICP-MS method, which demonstrates that
1Cu
and
2Cu
complexes are not efficiently accumulated inside the cell. Furthermore, the role of ROS in lipid peroxidation was established. The above-mentioned factors may clearly indicate the contribution of ROS generated by the studied copper(
ii
) complexes to colonic cell damage, which can lead to a carcinogenesis process. This study may be an important step to recognize and understand the mechanism of colon cancer initiation.
The ability of Cu(
ii
) complexes with FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) to produce reactive oxygen species (ROS) was determined.</description><identifier>ISSN: 1756-5901</identifier><identifier>EISSN: 1756-591X</identifier><identifier>DOI: 10.1039/c9mt00179d</identifier><language>eng</language><ispartof>Metallomics, 2019-12, Vol.11 (12), p.266-277</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids></links><search><creatorcontrib>Lesiów, Monika Katarzyna</creatorcontrib><creatorcontrib>Komarnicka, Urszula Katarzyna</creatorcontrib><creatorcontrib>Kyzio, Agnieszka</creatorcontrib><creatorcontrib>Bie ko, Alina</creatorcontrib><creatorcontrib>Pietrzyk, Piotr</creatorcontrib><title>ROS-mediated lipid peroxidation as a result of Cu() interaction with FomA protein fragments of : relevance to colorectal carcinogenesis</title><title>Metallomics</title><description>The ability of the studied FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) with copper(
ii
) ions (Cu(
ii
)-Ac-KGHGNGEEGTPTVHNE-NH
2
(
1Cu
) and its cyclic analogue Cu(
ii
)-cyclo(KGHGNGEEGTPTVHNE) (
2Cu
)) to induce reactive oxygen species (ROS) generation, as a result of red-ox processes, was determined by UV-Vis, luminescence methods, spin trapping and cyclic voltamperometry. The contribution of
1
O
2
and &z.rad;OH to DNA degradation was proved using gel electrophoresis. Furthermore, the pronounced generation of ROS by mouse colon carcinoma cells (CT26) stimulated by both copper(
ii
) complexes was confirmed. A fluorescence method allowed the total amounts of ROS generated inside the CT26 cells to be detected, while the spin trapping technique proved that free radicals mainly attached to the membrane surface. These last results are in agreement with the data obtained from the ICP-MS method, which demonstrates that
1Cu
and
2Cu
complexes are not efficiently accumulated inside the cell. Furthermore, the role of ROS in lipid peroxidation was established. The above-mentioned factors may clearly indicate the contribution of ROS generated by the studied copper(
ii
) complexes to colonic cell damage, which can lead to a carcinogenesis process. This study may be an important step to recognize and understand the mechanism of colon cancer initiation.
The ability of Cu(
ii
) complexes with FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) to produce reactive oxygen species (ROS) was determined.</description><issn>1756-5901</issn><issn>1756-591X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj7tKBEEQRRtRcH0k5kKZaTDazTi7jJksLmaCGpgNRXfNWtIvqnt9fIG_rSuimUb3wjk3uEodGH1qdNuf2T5Urc2sdxtqYmbdtOl687D507XZVjulPGk9Pde6m6j325u7JpBjrOTAc2YHmSS9ssPKKQIWQBAqK18hjTBfHZ8Ax0qC9ou_cH2ERQqXkCVV4gij4DJQrGXtX3xuPT1jtAQ1gU0-CdmKHiyK5ZiWFKlw2VNbI_pC-9-5qw4XV_fz60aKHbJwQHkbft-1__Ojv_iQ3dh-ABMNYLo</recordid><startdate>20191211</startdate><enddate>20191211</enddate><creator>Lesiów, Monika Katarzyna</creator><creator>Komarnicka, Urszula Katarzyna</creator><creator>Kyzio, Agnieszka</creator><creator>Bie ko, Alina</creator><creator>Pietrzyk, Piotr</creator><scope/></search><sort><creationdate>20191211</creationdate><title>ROS-mediated lipid peroxidation as a result of Cu() interaction with FomA protein fragments of : relevance to colorectal carcinogenesis</title><author>Lesiów, Monika Katarzyna ; Komarnicka, Urszula Katarzyna ; Kyzio, Agnieszka ; Bie ko, Alina ; Pietrzyk, Piotr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c9mt00179d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Lesiów, Monika Katarzyna</creatorcontrib><creatorcontrib>Komarnicka, Urszula Katarzyna</creatorcontrib><creatorcontrib>Kyzio, Agnieszka</creatorcontrib><creatorcontrib>Bie ko, Alina</creatorcontrib><creatorcontrib>Pietrzyk, Piotr</creatorcontrib><jtitle>Metallomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lesiów, Monika Katarzyna</au><au>Komarnicka, Urszula Katarzyna</au><au>Kyzio, Agnieszka</au><au>Bie ko, Alina</au><au>Pietrzyk, Piotr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ROS-mediated lipid peroxidation as a result of Cu() interaction with FomA protein fragments of : relevance to colorectal carcinogenesis</atitle><jtitle>Metallomics</jtitle><date>2019-12-11</date><risdate>2019</risdate><volume>11</volume><issue>12</issue><spage>266</spage><epage>277</epage><pages>266-277</pages><issn>1756-5901</issn><eissn>1756-591X</eissn><abstract>The ability of the studied FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) with copper(
ii
) ions (Cu(
ii
)-Ac-KGHGNGEEGTPTVHNE-NH
2
(
1Cu
) and its cyclic analogue Cu(
ii
)-cyclo(KGHGNGEEGTPTVHNE) (
2Cu
)) to induce reactive oxygen species (ROS) generation, as a result of red-ox processes, was determined by UV-Vis, luminescence methods, spin trapping and cyclic voltamperometry. The contribution of
1
O
2
and &z.rad;OH to DNA degradation was proved using gel electrophoresis. Furthermore, the pronounced generation of ROS by mouse colon carcinoma cells (CT26) stimulated by both copper(
ii
) complexes was confirmed. A fluorescence method allowed the total amounts of ROS generated inside the CT26 cells to be detected, while the spin trapping technique proved that free radicals mainly attached to the membrane surface. These last results are in agreement with the data obtained from the ICP-MS method, which demonstrates that
1Cu
and
2Cu
complexes are not efficiently accumulated inside the cell. Furthermore, the role of ROS in lipid peroxidation was established. The above-mentioned factors may clearly indicate the contribution of ROS generated by the studied copper(
ii
) complexes to colonic cell damage, which can lead to a carcinogenesis process. This study may be an important step to recognize and understand the mechanism of colon cancer initiation.
The ability of Cu(
ii
) complexes with FomA protein fragments of
Fusobacterium nucleatum
(
Fn
) to produce reactive oxygen species (ROS) was determined.</abstract><doi>10.1039/c9mt00179d</doi><tpages>12</tpages></addata></record> |
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ispartof | Metallomics, 2019-12, Vol.11 (12), p.266-277 |
issn | 1756-5901 1756-591X |
language | eng |
recordid | cdi_rsc_primary_c9mt00179d |
source | Oxford University Press Journals All Titles (1996-Current) |
title | ROS-mediated lipid peroxidation as a result of Cu() interaction with FomA protein fragments of : relevance to colorectal carcinogenesis |
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