Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/37019
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dc.contributor.authorTokgun, O.-
dc.contributor.authorKarakas, D.E.-
dc.contributor.authorTan, Semih-
dc.contributor.authorKaragür, E.R.-
dc.contributor.authorİnal, B.-
dc.contributor.authorAkca, H.-
dc.contributor.authorDurap, F.-
dc.date.accessioned2021-02-02T09:23:37Z-
dc.date.available2021-02-02T09:23:37Z-
dc.date.issued2020-
dc.identifier.issn0366-6352-
dc.identifier.urihttps://hdl.handle.net/11499/37019-
dc.identifier.urihttps://doi.org/10.1007/s11696-020-01129-x-
dc.description.abstractLung cancer is one of the major causes of cancer-related deaths in the world. Non-small-cell lung cancer (NSCLC) is the most common type of lung cancer, and small-cell lung cancer (SCLC) is the most aggressive subtype of lung cancer. Proper therapies for SCLC have not yet been developed. However, new molecules have been designed and big innovation in treating SCLC has been achieved. Platinum-based antitumor drugs like cisplatin and carboplatin have several disadvantages including side effects, cisplatin-resistant tumors and limited solubility in aqueous media. Thus, two novel chiral aminoalcohol-based bis(phosphinite) ligands containing (?6-p-cymene)-Ru(II)-phosphinite and bis(phosphinite)–Pd(II) complexes were synthesized and evaluated for anticancer activity. In this study, the results showed that complex 1 has the strongest cytotoxic effects on SCLC and NSCLC cell lines. On the other hand, cisplatin, ruthenium and palladium complexes are capable to induce apoptosis. Especially, complexes 1 and 2 can induce apoptosis for both SCLC and NSCLC. When compared to the qRT-PCR and TUNEL results, we obtained a significant correlation between apoptotic index and p21, Bax gene expressions. This work revealed the potential of the synthesized complexes as anticancer agents with cytotoxic and pro-apoptotic activity as leading compounds for further anticancer researches. © 2020, Institute of Chemistry, Slovak Academy of Sciences.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofChemical Papersen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBaxen_US
dc.subjectNSCLCen_US
dc.subjectp21en_US
dc.subjectPalladiumen_US
dc.subjectPhosphiniteen_US
dc.subjectRutheniumen_US
dc.subjectSCLCen_US
dc.titleNovel ruthenium and palladium complexes as potential anticancer molecules on SCLC and NSCLC cell linesen_US
dc.typeArticleen_US
dc.identifier.volume74en_US
dc.identifier.issue9en_US
dc.identifier.startpage2883-
dc.identifier.startpage2883en_US
dc.identifier.endpage2892en_US
dc.authorid0000-0002-5609-9594-
dc.identifier.doi10.1007/s11696-020-01129-x-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85081330981en_US
dc.identifier.wosWOS:000540601300014en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.grantfulltextnone-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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