| Literature DB >> 27572677 |
Shou-Cheng Wu1, Chung-Yen Lu1, Yi-Lin Chen1, Feng-Chun Lo1, Ting-Yin Wang1, Yu-Jen Chen2, Shyng-Shiou Yuan3, Wen-Feng Liaw1, Yun-Ming Wang2,4.
Abstract
Nitric oxide (NO) is an important cellular signaling molecule that modulates various physiological activities. Angiogenesis-promoting activities of NO-donor drugs have been explored in both experimental and clinical studies. In this study, a structurally well characterized and water-soluble neutral {Fe(NO)2}(9) DNIC [(S(CH2)2OH)(S(CH2)2NH3)Fe(NO)2] (DNIC 2) was synthesized to serve as a NO-donor species. The antitumor activity of DNIC 2 was determined by MTT assay, confocal imaging, and Annexin-V/PI staining. The IC50 values of DNIC 2 were 18.8, 42.9, and 38.6 μM for PC-3, SKBR-3, and CRL5866 tumor cells, respectively. Moreover, DNIC 2 promoted apoptotic cell death via activation of apoptosis-associated proteins and inhibition of survival associated proteins. In particular, DNIC 2 treatment suppressed PC-3 tumor growth by 2.34- and 19.3-fold at 7 and 21 days, in comparison with the control group. These results indicate that water-soluble DNIC 2 may serve as a promising drug for cancer therapy.Entities:
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Year: 2016 PMID: 27572677 DOI: 10.1021/acs.inorgchem.6b01562
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165