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DOI 10.1080/07391102.2018.1527724

Медицинская библиотека · Journal of biomolecular structure & dynamics · 2018

Antiproliferative activity of morpholine-based compounds on MCF-7 breast cancer, colon carcinoma C26, and normal fibroblast NIH-3T3 cell lines and study of their binding affinity to calf thymus-DNA and bovine serum albumin.

Hosseini-Kharat Mahboubeh, Rahimi Rahmatollah, Zargarian Davit, Mehri Lighvan Zohreh, Momtazi-Borojeni Amir Abbas, Sharifi Tayebeh, Abdollahi Elham, Tavakol Hossein, Mohammadi Tecush

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Аннотация

This report describes the results of a study on the antiproliferative activity of the morpholine-based ligand 1,3-bis(1-morpholinothiocarbonyl)benzene (HL) and its nickel(II) complex (NiL) against human breast cancer cells (MCF-7), colon carcinoma cells (C26), and normal fibroblast NIH-3T3 cells. NiL showed better cytotoxicity on both cancerous cells relative to normal cells in vitro with the highest selective index of 2.22 in MCF-7 cells. The interaction of both compounds with calf thymus DNA (CT DNA) and bovine serum albumin (BSA) was studied using various spectroscopic techniques and analytical methods such as UV - vis titrations, thermal denaturation, circular dichroism, competitive fluorescent intercalator displacement assays, as well as molecular modeling. The fluorescence intensity of the probe molecule increases clearly when HL and NiL are added to the methylene blue (MB)-DNA system. Furthermore, the binding of HL and NiL quenches the BSA fluorescence, revealing a 1:1 interaction with a binding constant of about 105 M-1. Communicated by Ramaswamy H. Sarma.

Для цитирования: Hosseini-Kharat Mahboubeh, Rahimi Rahmatollah, Zargarian Davit, Mehri Lighvan Zohreh, Momtazi-Borojeni Amir Abbas, Sharifi Tayebeh, Abdollahi Elham, Tavakol Hossein, Mohammadi Tecush. Antiproliferative activity of morpholine-based compounds on MCF-7 breast cancer, colon carcinoma C26, and normal fibroblast NIH-3T3 cell lines and study of their binding affinity to calf thymus-DNA and bovine serum albumin.. Journal of biomolecular structure & dynamics. 2018. DOI: 10.1080/07391102.2018.1527724.

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