Insights into the strong in-vitro anticancer effects for bis(triphenylphosphane)iminium compounds having perchlorate, tetrafluoridoborate and bis(chlorido)argentate anions
Three new compounds containing the bis(triphenylphosphane)iminium cation (PPN+) with ClO4−, BF4− and [AgCl2]− as counter anions have been synthesized and structurally characterized. The two derivatives with ClO4− and BF4− were found to be isostructural by single crystal X-ray diffraction. Interestin...
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Veröffentlicht in: | Journal of inorganic biochemistry 2015-12, Vol.153, p.346-354 |
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creator | Folda, Alessandra Scalcon, Valeria Ghazzali, Mohamed Jaafar, Mohammed H. Khan, Rais Ahmad Casini, Angela Citta, Anna Bindoli, Alberto Rigobello, Maria Pia Al-Farhan, Khalid Alsalme, Ali Reedijk, Jan |
description | Three new compounds containing the bis(triphenylphosphane)iminium cation (PPN+) with ClO4−, BF4− and [AgCl2]− as counter anions have been synthesized and structurally characterized. The two derivatives with ClO4− and BF4− were found to be isostructural by single crystal X-ray diffraction. Interestingly, the three compounds show extremely potent antiproliferative effects against the human cancer cell line SKOV3. To gain insights into the possible mechanisms of biological action, several intracellular targets have been considered. Thus, DNA binding has been evaluated, as well as the effects of the compounds on the mitochondrial function. Furthermore, the compounds have been tested as possible inhibitors of the seleno-enzyme thioredoxin reductase.
Salts of the bis(triphenylphosphane)iminium cation show cancer cell cytotoxicity, DNA binding, mitochondrial bioenergetic impairment and inhibition of the enzyme thioredoxin reductase. [Display omitted]
•Three new compounds with the PPN cation have been prepared and structurally characterized.•The compounds show strong antiproliferative effects against the human cancer cell line SKOV3.•The DNA binding and the effects of the compounds on the mitochondrial function are studied.•The compounds were tested as possible inhibitors of thioredoxin reductase. |
doi_str_mv | 10.1016/j.jinorgbio.2015.08.030 |
format | Article |
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Salts of the bis(triphenylphosphane)iminium cation show cancer cell cytotoxicity, DNA binding, mitochondrial bioenergetic impairment and inhibition of the enzyme thioredoxin reductase. [Display omitted]
•Three new compounds with the PPN cation have been prepared and structurally characterized.•The compounds show strong antiproliferative effects against the human cancer cell line SKOV3.•The DNA binding and the effects of the compounds on the mitochondrial function are studied.•The compounds were tested as possible inhibitors of thioredoxin reductase.</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2015.08.030</identifier><identifier>PMID: 26384162</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Anti-cancer compounds ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Cell Line, Tumor ; Crystal structure ; DNA - chemistry ; DNA binding ; Enzyme Inhibitors - chemical synthesis ; Enzyme Inhibitors - chemistry ; Enzyme Inhibitors - pharmacology ; Humans ; Isomorphism ; Mitochondria ; Mitochondria - drug effects ; Molecular Sequence Data ; Organometallic Compounds - chemical synthesis ; Organometallic Compounds - chemistry ; Organometallic Compounds - pharmacology ; Protein Binding ; Rats ; Silver Compounds - chemistry ; Thioredoxin reductase ; Thioredoxin-Disulfide Reductase - antagonists & inhibitors ; Thioredoxin-Disulfide Reductase - chemistry ; Thioredoxin-Disulfide Reductase - metabolism</subject><ispartof>Journal of inorganic biochemistry, 2015-12, Vol.153, p.346-354</ispartof><rights>2015</rights><rights>Copyright © 2015. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c527t-b1e213ec6f1c00b1a9a3bccacfa499e72e68e8f228f1ddd0c104b05a9180fa23</citedby><cites>FETCH-LOGICAL-c527t-b1e213ec6f1c00b1a9a3bccacfa499e72e68e8f228f1ddd0c104b05a9180fa23</cites><orcidid>0000-0002-6739-8514</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinorgbio.2015.08.030$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26384162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Folda, Alessandra</creatorcontrib><creatorcontrib>Scalcon, Valeria</creatorcontrib><creatorcontrib>Ghazzali, Mohamed</creatorcontrib><creatorcontrib>Jaafar, Mohammed H.</creatorcontrib><creatorcontrib>Khan, Rais Ahmad</creatorcontrib><creatorcontrib>Casini, Angela</creatorcontrib><creatorcontrib>Citta, Anna</creatorcontrib><creatorcontrib>Bindoli, Alberto</creatorcontrib><creatorcontrib>Rigobello, Maria Pia</creatorcontrib><creatorcontrib>Al-Farhan, Khalid</creatorcontrib><creatorcontrib>Alsalme, Ali</creatorcontrib><creatorcontrib>Reedijk, Jan</creatorcontrib><title>Insights into the strong in-vitro anticancer effects for bis(triphenylphosphane)iminium compounds having perchlorate, tetrafluoridoborate and bis(chlorido)argentate anions</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>Three new compounds containing the bis(triphenylphosphane)iminium cation (PPN+) with ClO4−, BF4− and [AgCl2]− as counter anions have been synthesized and structurally characterized. The two derivatives with ClO4− and BF4− were found to be isostructural by single crystal X-ray diffraction. Interestingly, the three compounds show extremely potent antiproliferative effects against the human cancer cell line SKOV3. To gain insights into the possible mechanisms of biological action, several intracellular targets have been considered. Thus, DNA binding has been evaluated, as well as the effects of the compounds on the mitochondrial function. Furthermore, the compounds have been tested as possible inhibitors of the seleno-enzyme thioredoxin reductase.
Salts of the bis(triphenylphosphane)iminium cation show cancer cell cytotoxicity, DNA binding, mitochondrial bioenergetic impairment and inhibition of the enzyme thioredoxin reductase. [Display omitted]
•Three new compounds with the PPN cation have been prepared and structurally characterized.•The compounds show strong antiproliferative effects against the human cancer cell line SKOV3.•The DNA binding and the effects of the compounds on the mitochondrial function are studied.•The compounds were tested as possible inhibitors of thioredoxin reductase.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Anti-cancer compounds</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Crystal structure</subject><subject>DNA - chemistry</subject><subject>DNA binding</subject><subject>Enzyme Inhibitors - chemical synthesis</subject><subject>Enzyme Inhibitors - chemistry</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Humans</subject><subject>Isomorphism</subject><subject>Mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Molecular Sequence Data</subject><subject>Organometallic Compounds - chemical synthesis</subject><subject>Organometallic Compounds - chemistry</subject><subject>Organometallic Compounds - pharmacology</subject><subject>Protein Binding</subject><subject>Rats</subject><subject>Silver Compounds - chemistry</subject><subject>Thioredoxin reductase</subject><subject>Thioredoxin-Disulfide Reductase - antagonists & inhibitors</subject><subject>Thioredoxin-Disulfide Reductase - chemistry</subject><subject>Thioredoxin-Disulfide Reductase - metabolism</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1O3DAQgC3Uqmyhr9DmCFIT_JNskiNC_UFC6oW75djjzawSO7WdlXgmXrJmF7j25PHMNzMafYR8Y7RilG1v9tUenQ-7AX3FKWsq2lVU0DOyYV0rSiHq-gPZZJKXlIn6nHyOcU8pbZq6_UTO-VZ0dS5uyPO9i7gbUyzQJV-kEYqYgne7_C8PmMNCuYRaOQ2hAGtBZ9b6UAwYr1LAZQT3NC2jj8uoHFzjjA7XudB-XvzqTCxGdcA8b4Ggx8kHleB7kSAFZafVBzR-OCbzHnMceqRy-lqFHbh0KqF38ZJ8tGqK8OX1vSCPP3883v0uH_78ur-7fSh1w9tUDgw4E6C3lmlKB6Z6JQatlbaq7ntoOWw76CznnWXGGKoZrQfaqJ511CouLsjVaewS_N8VYpIzRg3TlM_za5SsbVjfs5q1GW1PqA4-xgBWLgFnFZ4ko_JFlNzLd1HyRZSkncyicufX1yXrMIN573szk4HbEwD50gNCkFEjZAsGQ3Ygjcf_LvkH2CivzQ</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Folda, Alessandra</creator><creator>Scalcon, Valeria</creator><creator>Ghazzali, Mohamed</creator><creator>Jaafar, Mohammed H.</creator><creator>Khan, Rais Ahmad</creator><creator>Casini, Angela</creator><creator>Citta, Anna</creator><creator>Bindoli, Alberto</creator><creator>Rigobello, Maria Pia</creator><creator>Al-Farhan, Khalid</creator><creator>Alsalme, Ali</creator><creator>Reedijk, Jan</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6739-8514</orcidid></search><sort><creationdate>20151201</creationdate><title>Insights into the strong in-vitro anticancer effects for bis(triphenylphosphane)iminium compounds having perchlorate, tetrafluoridoborate and bis(chlorido)argentate anions</title><author>Folda, Alessandra ; Scalcon, Valeria ; Ghazzali, Mohamed ; Jaafar, Mohammed H. ; Khan, Rais Ahmad ; Casini, Angela ; Citta, Anna ; Bindoli, Alberto ; Rigobello, Maria Pia ; Al-Farhan, Khalid ; Alsalme, Ali ; Reedijk, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c527t-b1e213ec6f1c00b1a9a3bccacfa499e72e68e8f228f1ddd0c104b05a9180fa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Anti-cancer compounds</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>Crystal structure</topic><topic>DNA - chemistry</topic><topic>DNA binding</topic><topic>Enzyme Inhibitors - chemical synthesis</topic><topic>Enzyme Inhibitors - chemistry</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Humans</topic><topic>Isomorphism</topic><topic>Mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Molecular Sequence Data</topic><topic>Organometallic Compounds - chemical synthesis</topic><topic>Organometallic Compounds - chemistry</topic><topic>Organometallic Compounds - pharmacology</topic><topic>Protein Binding</topic><topic>Rats</topic><topic>Silver Compounds - chemistry</topic><topic>Thioredoxin reductase</topic><topic>Thioredoxin-Disulfide Reductase - antagonists & inhibitors</topic><topic>Thioredoxin-Disulfide Reductase - chemistry</topic><topic>Thioredoxin-Disulfide Reductase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Folda, Alessandra</creatorcontrib><creatorcontrib>Scalcon, Valeria</creatorcontrib><creatorcontrib>Ghazzali, Mohamed</creatorcontrib><creatorcontrib>Jaafar, Mohammed H.</creatorcontrib><creatorcontrib>Khan, Rais Ahmad</creatorcontrib><creatorcontrib>Casini, Angela</creatorcontrib><creatorcontrib>Citta, Anna</creatorcontrib><creatorcontrib>Bindoli, Alberto</creatorcontrib><creatorcontrib>Rigobello, Maria Pia</creatorcontrib><creatorcontrib>Al-Farhan, Khalid</creatorcontrib><creatorcontrib>Alsalme, Ali</creatorcontrib><creatorcontrib>Reedijk, Jan</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Folda, Alessandra</au><au>Scalcon, Valeria</au><au>Ghazzali, Mohamed</au><au>Jaafar, Mohammed H.</au><au>Khan, Rais Ahmad</au><au>Casini, Angela</au><au>Citta, Anna</au><au>Bindoli, Alberto</au><au>Rigobello, Maria Pia</au><au>Al-Farhan, Khalid</au><au>Alsalme, Ali</au><au>Reedijk, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insights into the strong in-vitro anticancer effects for bis(triphenylphosphane)iminium compounds having perchlorate, tetrafluoridoborate and bis(chlorido)argentate anions</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>153</volume><spage>346</spage><epage>354</epage><pages>346-354</pages><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>Three new compounds containing the bis(triphenylphosphane)iminium cation (PPN+) with ClO4−, BF4− and [AgCl2]− as counter anions have been synthesized and structurally characterized. The two derivatives with ClO4− and BF4− were found to be isostructural by single crystal X-ray diffraction. Interestingly, the three compounds show extremely potent antiproliferative effects against the human cancer cell line SKOV3. To gain insights into the possible mechanisms of biological action, several intracellular targets have been considered. Thus, DNA binding has been evaluated, as well as the effects of the compounds on the mitochondrial function. Furthermore, the compounds have been tested as possible inhibitors of the seleno-enzyme thioredoxin reductase.
Salts of the bis(triphenylphosphane)iminium cation show cancer cell cytotoxicity, DNA binding, mitochondrial bioenergetic impairment and inhibition of the enzyme thioredoxin reductase. [Display omitted]
•Three new compounds with the PPN cation have been prepared and structurally characterized.•The compounds show strong antiproliferative effects against the human cancer cell line SKOV3.•The DNA binding and the effects of the compounds on the mitochondrial function are studied.•The compounds were tested as possible inhibitors of thioredoxin reductase.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26384162</pmid><doi>10.1016/j.jinorgbio.2015.08.030</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6739-8514</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Anti-cancer compounds Antineoplastic Agents - chemical synthesis Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Cell Line, Tumor Crystal structure DNA - chemistry DNA binding Enzyme Inhibitors - chemical synthesis Enzyme Inhibitors - chemistry Enzyme Inhibitors - pharmacology Humans Isomorphism Mitochondria Mitochondria - drug effects Molecular Sequence Data Organometallic Compounds - chemical synthesis Organometallic Compounds - chemistry Organometallic Compounds - pharmacology Protein Binding Rats Silver Compounds - chemistry Thioredoxin reductase Thioredoxin-Disulfide Reductase - antagonists & inhibitors Thioredoxin-Disulfide Reductase - chemistry Thioredoxin-Disulfide Reductase - metabolism |
title | Insights into the strong in-vitro anticancer effects for bis(triphenylphosphane)iminium compounds having perchlorate, tetrafluoridoborate and bis(chlorido)argentate anions |
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