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Cytotoxicity and Apoptosis Inducing Activities of 2-Amino-4H-Chromene-3-Carbonitrile Derivatives Loaded on Gold Nanoparticles Against Human Breast Cancer Cell Line T47d Publisher



Saffari Z1 ; Zarabi MF2, 5 ; Aryapour H3 ; Foroumadi A4 ; Farhangi A5 ; Ghassemi S5 ; Akbarzadeh A5
Authors
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Authors Affiliations
  1. 1. Department of Biochemistry, Science and Research Branch, Islamic Azad University, Kordestan, Iran
  2. 2. Department of Chemistry, Zanjan University, Zanjan, Iran
  3. 3. Department of Biology, Golestan University, Gorgan, Iran
  4. 4. Department of Medicinal Chemistry, Research Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Pilot NanoBiotechnology, Pasteur Institute of Iran, No. 69, 12 Farvardin Street, Jomhoori Avenue, Tehran, 13169-43551, Iran

Source: Indian Journal of Clinical Biochemistry Published:2015


Abstract

Chemotherapy drugs, used for prevention of uncontrolled cell proliferation in certain tissues as well as inducing apoptosis in tumor cells, are important candidates for treatment of cancer. The synthesized 2-amino-4H-chromene-3-carbonitrile derivatives effective on cancerous cells resistant to other drugs such as Paclitaxel were used due to their ability in induction of apoptosis. The growth inhibitory and inducing apoptosis activities were determined. In order to make it target-oriented, the best compound was conjugated with gold nanoparticles (NPs) by aspartic acid with chemical reduction method. Cytotoxicity effect of 2-amino-4H-chromene-3-carbonitrile derivatives against the T47D breast cancer cell line was determined by MTT assay. The synthesis of gold NPs was confirmed by transmission electron microscopy, UV–Vis and dynamic light scattering. To assess the effects of compounds on the process of apoptosis, staining methods with acridine orange–ethidium bromide and Hoechst staining by fluorescence microscopy and DNA fragmentation by the diphenylamine method were used. The synthesized compounds containing two NH2 groups on benzene rings, demonstrated more cytotoxicity effect. The effect of conjugation with gold NPs and the induction of apoptosis were studied with the best compound. The cytotoxicity effects of the synthesized 2-amino-4H-chromene-3-carbonitrile compounds were changed by replacement of NO2 group on thiol ring with different chemical groups on the benzene ring. Analyses of treated cell lines by conjugated and non-conjugated forms of compounds verified their ability in inducing apoptosis while conjugated form demonstrated higher apoptosis. © 2014, Association of Clinical Biochemists of India.