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New Copper (II), Palladium (II), and Platinum (II) 2-Acetylpyrazine Tert-Butylthiosemicarbazone Complexes: Inhibition of Human Topoisomerase IIα and Activity against Breast Cancer Cells

DOI: 10.4236/ojmc.2022.121001, PP. 1-13

Keywords: Topoisomerase, Breast Cancer, α-(N)-Heterocyclic Thiosemicarbazones

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Abstract:

The new ligand, 2-acetylpyrazine-tertbutylthiosemicarbazone (APZ-tBTSC), and its Cu(II), Pd(II) and Pt(II) complexes have been synthesized. This ligand coordinates to the metal ions in a tridentate monoanionic fashion forming monometallic complexes with the formula [M(APZ-tBTSC)Cl]. The ligand and the three metal complexes [Cu(APZ-tBTSC)Cl], [Pd(APZ-tBTSC)Cl], and [Pt(APZ-tBTSC)Cl] were tested for anti-proliferative biological behavior with a panel of seven microbes, and the copper and palladium complexes were found to be highly active against Gram positive bacteria. The 4 compounds were also tested in human topoisomerase IIα DNA relaxation assays and all three metal complexes had topoisomerase inhibition at a concentration between 4 - 6 micro-molar. The 4 compounds were also tested for activity with the HEK293T cell line and also the breast cell cancer line, MDA-MB-231. The most effective compound for activity against the HEK293T cell line was the [Cu(APZ-tBTSC)Cl] complex, and the MDA-MB-231 breast cancer cell line was the [Pt(APZ-tBTSC)Cl] complex.

References

[1]  Beraldo, H. and Gambino, D. (2004) The Wide Pharmacological Versatility of Semicarbazones, Thiosemicarbazones and Their Metal Complexes. Mini-Reviews in Medicinal Chemistry, 4, 31-39.
https://doi.org/10.2174/1389557043487484
[2]  Koch, O. and Stuttgen, G. (1950) Clinical and Experimental Studies on the Effects of Thiosemicarbazones. Naunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 210, 409-423.
https://doi.org/10.1007/BF00246392
[3]  Padhye, S. and Kauffman, G.B. (1985) Transition Metal Complexes of Semicarbazones and Thiosemicarbazones. Coordination Chemistry Reviews, 63, 127-160.
https://doi.org/10.1016/0010-8545(85)80022-9
[4]  Casas, J.S., Garcia-Tasende, M.S. and Sordo, J. (2000) Main Group Metal Complexes of Semicarbazones and Thiosemicarbazones. A Structural Review. Coordination Chemistry Reviews, 209, 197-261.
https://doi.org/10.1016/S0010-8545(00)00363-5
[5]  Yu, Y., Kalinowski, D.S., Kovacevic, Z., Siafakas, A.R., Jansson, P.J., Stefani, C., Lovejoy, D.B., Sharpe, P.C., Bernhardt, P.V. and Richardson, D.R. (2009) Thiosemicarbazones from the Old to New: Iron Chelators That Are More than Just Ribonucleotide Reductase Inhibitors. Journal of Medicinal Chemistry, 52, 5271-5294.
https://doi.org/10.1021/jm900552r
[6]  Matesanz, A. and Souza, P. (2009) α-N-Heterocyclic Thiosemicarbazone Derivatives as Potential Antitumor Agents: A Structure-Activity Relationship. Mini-Reviews in Medicinal Chemistry, 9, 1389-1396.
https://doi.org/10.2174/138955709789957422
[7]  Moorthy, N., Cerquiera, N., Ramos, M. and Fernandez P. (2013) Development of Ribonucleotide Reductase Inhibitor: A Review on Structure Activity Relationships. Mini-Reviews in Medicinal Chemistry, 13, 1862-1872.
https://doi.org/10.2174/13895575113136660090
[8]  Finch, R.A., Liu, M., Grill, S.P., Rose, W.C., Loomis, R., Vasquez, K.M., Cheng, Y.C. and Sartorelli, A.C. (2000) Triapine (3-aminopyridine-2-carboxaldehyde-thiosemicarbazone): A Potent Inhibitor of Ribonucleotide Reductase Activity with Broad Spectrum Antitumor Activity. Biochemical pharmacology, 59, 983-991.
https://doi.org/10.1016/S0006-2952(99)00419-0
[9]  Knox, J.J., Hotte, S.J., Kollmannsberger, C., Winquist, E., Fisher, B. and Eisenhauer, E.A. (2007) Phase II Study of Triapine® in Patients with Metastatic Renal Cell Carcinoma: A Trial of the National Cancer Institute of Canada Clinical Trials Group (NCIC IND. 161). Investigational New Drugs, 25, 471-477.
https://doi.org/10.1007/s10637-007-9044-9
[10]  Ma, B., Goh, B.C., Tan, E.H., Lam, K.C., Soo, R., Leong, S.S., et al. (2008) A Multicenter Phase II Trial of 3-aminopyridine-2-carboxaldehyde Thiosemicarbazone (3-AP, Triapine®) and Gemcitabine in Advanced Non-Small-Cell Lung Cancer with Pharmacokinetic Evaluation Using Peripheral Blood Mononuclear Cells. Investigational New Drugs, 26, 169-173.
https://doi.org/10.1007/s10637-007-9085-0
[11]  Jansson, P.J., Sharpe, P.C., Bernhardt, P.V. and Richardson, D.R. (2010) Novel Thiosemicarbazones of the ApT and DpT Series and Their Copper Complexes: Identification of Pronounced Redox Activity and Characterization of Their Antitumor Activity. Journal of Medicinal Chemistry, 53, 5759-5769.
https://doi.org/10.1021/jm100561b
[12]  Zeglis, B.M., Divilov, V. and Lewis, J.S. (2011) Role of Metalation in the Topoisomerase IIα Inhibition and Antiproliferation Activity of a Series of α-Heterocyclic-N4-Substituted Thiosemicarbazones and Their Cu(II) Complexes. Journal of Medicinal Chemistry, 54, 2391-2398.
https://doi.org/10.1021/jm101532u
[13]  Yalowich, J.C., Wu, X., Zhang, R., Kanagasabai, R., Hornbaker, M. and Hasinoff, B.B. (2012) The Anticancer Thiosemicarbazones Dp44mT and Triapine Lack Inhibitory Effects as Catalytic Inhibitors or Poisons of DNA Topoisomerase IIα. Biochemical Pharmacology, 84, 52-58.
https://doi.org/10.1016/j.bcp.2012.03.021
[14]  Wilson, J.T., Jiang, X., McGill, B.C., Lisic, E.C. and Deweese, J.E. (2016) Examination of the Impact of Copper(II) α-(N)-Heterocyclic Thiosemicarbazone Complexes on DNA Topoisomerase IIα. Chemical Research in Toxicology, 29, 649-658.
https://doi.org/10.1021/acs.chemrestox.5b00471
[15]  Conner, J.D., Medawala, W., Stephens, M.T., Morris, W.H., Deweese, J.E., Kent, P.L., Rice, J.J., Jiang, X. and Lisic, E.C. (2016) Cu (II) Benzoylpyridine Thiosemicarbazone Complexes: Inhibition of Human Topoisomerase IIa and Activity against Breast Cancer Cells. Open Journal of Inorganic Chemistry, 6, 146-154.
https://doi.org/10.4236/ojic.2016.62010
[16]  Lisic, E.C., Rand, V.G., Ngo, L., Kent, P., Rice, J., Gerlach, D., Papish, E.T. and Jiang. X. (2018) Cu(II) Propionyl-Thiazole Thiosemicarbazone Complexes: Crystal Structure, Inhibition of Human Topoisomerase IIα, and Activity against Breast Cancer Cells. Open Journal of Medicinal Chemistry, 8, 30-46.
https://doi.org/10.4236/ojmc.2018.82004
[17]  Morris, W.H., Ngo, L., Wilson, J.T., Medawala, W., Brown, A.R., Conner, J.D., Fabunmi, F., Cashman, D.J., Lisic, E.C., Yu, T., Deweese, J.E. and Jiang, X. (2019) Structural and Metal Ion Effects on Human Topoisomerase IIα Inhibition by α-(N)-Heterocyclic Thiosemicarbazones. Chemical Research in Toxicology, 32, 90-99.
https://doi.org/10.1021/acs.chemrestox.8b00204
[18]  Keck, J.M., Conner, J.D., Wilson, J.T., Jiang, X., Lisic, E.C. and Deweese, J.E. (2019) Clarifying the Mechanism of Copper(II) α-(N)-Heterocyclic Thiosemicarbazone Complexes on DNA Topoisomerase IIα and IIβ. Chemical Research in Toxicology, 32, 2135-2143.
https://doi.org/10.1021/acs.chemrestox.9b00311
[19]  Lisic, E.C., Werlein, A., Koch, A. and Conner, J. (2013) Synthesis and Anti-Microbial Studies of a Series of 3-Formyl-Chromone Thiosemicarbazone Ligands and Their Cu(II) Complexes Including the Potent Akt Inhibitor [Cu(FC-TSC)Cl2}. Journal of Undergraduate Chemistry Research, 12, 101.

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