Publication Type Journal Article
Title In vitro and in vivo biological characterization of the anti-proliferative potential of a cyclic trinuclear organotin(IV) complex
Authors Marta Martins Pedro V. Baptista Ana Soraia Mendo Claudia Correia Paula A. Videira Antonio Sebastiao Rodrigues J. Muthukumaran Teresa Santos-Silva Ana Silva M. Fátima C. Guedes da Silva Joana Gigante Antonio Duarte Malgorzata Gajewska A.R. Fernandes
Groups CCC
Journal MOLECULAR BIOSYSTEMS
Year 2016
Month
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Volume 12
Number 3
Pages 1015-1023
Abstract Identification of novel molecules that can selectively inhibit the growth of tumor cells, avoid causing side effects to patients and/or intrinsic or acquired resistance, usually associated with common chemotherapeutic agents, is of utmost importance. Organometallic compounds have gained importance in oncologic chemotherapy, such as organotin(IV) complexes. In this study, we assessed the anti-tumor activity of the cyclic trinuclear organotin(IV) complex with an aromatic oximehydroxamic acid group [nBu(2)Sn(L)](3)(H2L = N,2-dihydroxy-5-[N-hydroxyethanimidoyl]benzamide) - MG85 - and provided further characterization of its biological targets. We have previously shown the high anti-proliferative activity of this complex against human colorectal and hepatocellular carcinoma cell lines and lower cytotoxicity in neonatal non-tumor fibroblasts. MG85 induces tumor cell apoptosis and down-regulation of proteins related to tubulin dynamics (TCTP and COF1). Further characterization included the: (i) evaluation of interference in the cell cycle progression, including the expression of critical genes; (ii) affinity to DNA and the corresponding mode of binding; (iii) genotoxic potential in cells with deficient DNA repair pathways; and (iv) in vivo tumor reduction efficiency using mouse colorectal carcinoma xenografts.
DOI http://dx.doi.org/10.1039/c5mb00791g
ISBN
Publisher ROYAL SOC CHEMISTRY
Book Title
ISSN 1742-206X
EISSN 1742-2051
Conference Name
Bibtex ID ISI:000371039800032
Observations
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