2-Aminoanthraquinone substituted cyclotriphosphazene derivatives and their effect on non-small cell lung cancer cell lines

dc.contributor.authorCiftci, Gonul Yenilmez
dc.contributor.authorDemirel, Gizem Demir
dc.contributor.authorTurhal, Gulseren
dc.contributor.authorDemirkan, Busra
dc.contributor.authorDemiroğlu-Zergeroğlu, Asuman
dc.date.accessioned2025-10-29T11:27:31Z
dc.date.issued2023
dc.departmentFakülteler, Temel Bilimler Fakültesi, Moleküler Biyoloji ve Genetik Bölümü
dc.departmentFakülteler, Mühendislik Fakültesi, Çevre Mühendisliği Bölümü
dc.description.abstractAmong several, the lung cancer is the most common and lethal tumor in the worldwide. Wide- variety of drugs are available for the treatment of the disease. However, strong side effects and innate or gained resistance of tumor cells to existing agents leads researchers to develop alternative agents with more effective and less side effects. Anthraquinone-derived drugs such as doxorubicin, mitoxantrone, epirubicin, idarubicin, and valrubicin are currently used to cure various of cancers. In this concept, novel 2-aminoanthraquinone substituted cyclotriphosphazene compounds 5-7 have been synthesized by our group and have been fully characterized by means of FT-IR, MALDI-TOF MS, 1H- and 31P NMR spectroscopies. Furthermore, anti-carcinogenic potential of the compounds was investigated on non-small-cell Lung Carcinoma (NSCLC) cell lines and as well as non-tumoral mesothelial cells (MeT-5A). Results showed that compared to others, the most effective compound to reduce the viability of cancer cells and to induce apoptosis was compound 7. Significantly, compound 7 has showed selectivity to cancer cells rather than its normal counterpart.
dc.description.sponsorshipScientific and Technical Research Council of Turkey (TUBITAK) [117Z163]
dc.description.sponsorshipThe authors would like to thank the Scientific and Technical Research Council of Turkey (TUBITAK) (grant number: 117Z163) for financial support.
dc.identifier.doi10.1016/j.ica.2023.121744
dc.identifier.issn0020-1693
dc.identifier.issn1873-3255
dc.identifier.orcid0000-0002-0936-8368
dc.identifier.scopus2-s2.0-85170041334
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.1016/j.ica.2023.121744
dc.identifier.urihttps://hdl.handle.net/20.500.14854/10762
dc.identifier.volume558
dc.identifier.wosWOS:001077215600001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Science Sa
dc.relation.ispartofInorganica Chimica Acta
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subject2-Aminoanthraquinone
dc.subjectCyclotriphosphazene
dc.subjectNMR
dc.subjectCytotoxicity
dc.subjectNSCLC
dc.title2-Aminoanthraquinone substituted cyclotriphosphazene derivatives and their effect on non-small cell lung cancer cell lines
dc.typeArticle

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