The tremendous success of cisplatin, cis-[Pt(NH3)2Cl2], in human cancer chemotherapy has led to interest in the potential for complexes of another transition metal, Ru (II), to function as an anti-cancer agents. We have developed a class of ruthenium complexes which incorporate a redox-active intercalating ligand denoted tatpp. These ruthenium-tatpp complexes have been shown to tightly bind DNA and to cause DNA cleavage under conditions of low oxygen tension (hypoxia) and in the presence of common cellular reductants, e.g. glutathione. In our initial grant period, we have shown that mice implanted with either mouse melanoma (B16) or nude mice implanted with human non-small cell lung carcinoma (H358) tumor cells show arrested tumor growth and extended lifetimes when treated with two specific ruthenium-tatpp complexes. We have also shown that these complexes are cytotoxic towards a broad range of cancer cell lines but are considerably (~10 fold difference) less toxic to normal cells. Animal acute-toxicity studies show that chiral versions of these complexes are not appreciably toxic and can be safely be used and drugs. Thus all of our initial data suggests that this class of compounds may have potential an future chemotherapeutic drugs for cancer treatment. In our initial grant period, we established a number of structure-activity relationships and established that only complexes containing redox-active bridging ligands were promising drug candidates. In this proposal, we aim to prepare a number of new complexes in which both the reduction potential of the bridging ligand and the other anciallary ligands are varied to further delineate the structure-activity relationships for this class of compounds. The new complexes will be screened for DNA binding, DNA cleavage and cytotoxicty towards two cancer cells lines. Promising candidates will be further examined in animal models. In addition to establishing structure-activity relationships, we propose to examine the mechanism of DNA cleavage in detail using combination of EPR techniques and DNA product analysis studies. The unusual behavior under hypoxic conditions suggests a novel mechanism of action. We also will examine the detailed mechanism of chemical action for the DNA cleavage reaction and examine the biological pathways affected by drug treatment. In particular, we will examine the affect of these complexes on factors, e.g. HIF-1/2, VEGF, LDH-A, associated with hypoxic stress in both cells and in animals.

Public Health Relevance

We are developing a class of potential anti-cancer drugs based on ruthenium metal complexes in which one ligand is redox-active under common biological conditions. These compounds are able to arrest tumor growth in mice and show high specificity for killing tumor cells over normal cells. These compounds bind and cleave DNA and recently we have shown that they do so better under conditions of low oxygen tension (hypoxia). This is promising because tumor cells under hypoxic stress are one of the most difficult subpopulations of cancer cells to treat and few compounds show better activity under hypoxic conditions over normal conditions.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
2R15CA113747-02
Application #
7778988
Study Section
Drug Discovery and Molecular Pharmacology Study Section (DMP)
Program Officer
Misra, Raj N
Project Start
2005-04-01
Project End
2014-02-28
Budget Start
2010-03-05
Budget End
2014-02-28
Support Year
2
Fiscal Year
2010
Total Cost
$213,807
Indirect Cost
Name
University of Texas Arlington
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
064234610
City
Arlington
State
TX
Country
United States
Zip Code
76019
Shu, Yang; Breitbach, Zachary S; Dissanayake, Milan K et al. (2015) Enantiomeric separations of ruthenium (II) polypyridyl complexes using HPLC with cyclofructan chiral stationary phases. Chirality 27:64-70
Bhan, Arunoday; Hussain, Imran; Ansari, Khairul I et al. (2014) Histone methyltransferase EZH2 is transcriptionally induced by estradiol as well as estrogenic endocrine disruptors bisphenol-A and diethylstilbestrol. J Mol Biol 426:3426-41
Bhan, Arunoday; Hussain, Imran; Ansari, Khairul I et al. (2014) Bisphenol-A and diethylstilbestrol exposure induces the expression of breast cancer associated long noncoding RNA HOTAIR in vitro and in vivo. J Steroid Biochem Mol Biol 141:160-70
Bhan, Arunoday; Hussain, Imran; Ansari, Khairul I et al. (2013) Antisense transcript long noncoding RNA (lncRNA) HOTAIR is transcriptionally induced by estradiol. J Mol Biol 425:3707-22
Ansari, K I; Kasiri, S; Mandal, S S (2013) Histone methylase MLL1 has critical roles in tumor growth and angiogenesis and its knockdown suppresses tumor growth in vivo. Oncogene 32:3359-70
Kasiri, Sahba; Ansari, Khairul I; Hussain, Imran et al. (2013) Antisense oligonucleotide mediated knockdown of HOXC13 affects cell growth and induces apoptosis in tumor cells and over expression of HOXC13 induces 3D-colony formation. RSC Adv 3:3260-3269
Yadav, Abhishek; Janaratne, Thamara; Krishnan, Arthi et al. (2013) Regression of lung cancer by hypoxia-sensitizing ruthenium polypyridyl complexes. Mol Cancer Ther 12:643-53
Ansari, K I; Kasiri, S; Mishra, B P et al. (2012) Mixed lineage leukaemia-4 regulates cell-cycle progression and cell viability and its depletion suppresses growth of xenografted tumour in vivo. Br J Cancer 107:315-24
Shrestha, Bishakha; Ansari, Khairul I; Bhan, Arunoday et al. (2012) Homeodomain-containing protein HOXB9 regulates expression of growth and angiogenic factors, facilitates tumor growth in vitro and is overexpressed in breast cancer tissue. FEBS J 279:3715-3726
Ansari, Khairul I; Hussain, Imran; Kasiri, Sahba et al. (2012) HOXC10 is overexpressed in breast cancer and transcriptionally regulated by estrogen via involvement of histone methylases MLL3 and MLL4. J Mol Endocrinol 48:61-75

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