Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/39746
Title: DNA binding, cytotoxicity and mitochondria-mediated cell apoptosis induction of a new zinc(II) complex of 5-chloro-8-hydroxylquinoline
Authors: Zhang, Hai-Rong
Meng, Ting
Qin, Qi-Pin
Deng, Sheng-Ping
Cao, Qian-Qian
Han, Hong-Hua
Li, Ying-Bo
Zhang, Yun-Liang
Liu, Yan-Cheng
Liang, Hong
Keywords: Coordination chemistry;Halogenated quinoline;Zinc;DNA binding;Cytotoxicity;Cell apoptosis;Apoptosis
Issue Date: Dec-2016
Publisher: NISCAIR-CSIR, India
Abstract: A new zinc(II) complex (1) of 5-chloro-8-hydroxylquinoline (HClQ) has been synthesized and characterized by IR spectroscopy, ESI-MS spectrometry, elemental analysis and single crystal X-ray diffraction analysis. The DNA binding property of complex (1) has been investigated by UV-vis spectroscopy, circular dichroism spectroscopy and agarose gel electrophoresis. The results indicate that complex (1) binds with ct-DNA via an intercalative mode, and also exhibits DNA cleavage activity. The in vitro cytotoxicity of complex (1) has been screened by MTT assay against a series of tumor cell lines as well as HL-7702 normal liver cell line and, compared with that of cisplatin. Complex (1) shows lower cytotoxicity than cisplatin towards both the tumor cell lines and the normal liver cell line, except the BEL-7404 liver tumor cell line. The IC50 value of (1) towards BEL-7404 is 7.04±0.06 μM, which is lower than that of cisplatin (25.08±0.12 μM). This suggests that BEL-7404 is the most sensitive tumor cell line for (1). Complex (1) is found to induce cell apoptosis in the BEL-7404 cells by arresting the cell cycle at the S phase. The antitumor mechanism of (1) involves targeting the mitochondria-mediated pathway, since the ROS release and the cytoplasmic [Ca2+]c increase in the tested tumor cells after incubation with (1). Flow cytometry assay on the cellular level confirms that the dysfunction of the mitochondria (indicated by the loss of mitochondrial membrane potential) and the release of ROS and Ca2+, directly cause the activation of caspase cascade, including caspase-9 as the initiator and caspase-3 as the executor. These results strongly suggest that the central Zn(II) as the coordinating centre plays the key role in enhancing the antitumor activity and actuating the potential apoptotic pathway for this kind of halogenated quinoline derivatives.
Page(s): 1433-1442
URI: http://nopr.niscair.res.in/handle/123456789/39746
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.55A(12) [December 2016]

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IJCA 55A(12) 1433-1442_CIF.pdfSupplementary Data 1110.39 kBAdobe PDFView/Open


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