Key result
The 1,8 dinuclear platinum compound yields ~6-fold greater DNA cross-linking than cisplatin despite lower cytotoxicity.
Why the study?
The clinical side effects and drug resistance associated with cisplatin motivate the characterization of novel dinuclear platinum-based compounds as potential anticancer agents.
Novel dinuclear platinum complexes exhibit different DNA adduct sequence specificity and greater DNA cross-linking ability compared to cisplatin, warranting further investigation as potential chemotherapeutic agents.
These novel dinuclear Pt compounds show lower cytotoxicity but superior cross-linking versus cisplatin; leaves open their therapeutic potential pending in vivo studies.
BACKGROUND: The anti-tumour activity of cisplatin is thought to be a result of its capacity to form DNA adducts which prevent cellular processes such as DNA replication and transcription. These DNA adducts can effectively induce cancer cell death, however, there are a range of clinical side effects and drug resistance issues associated with its use. In this study, the biological properties of three novel dinuclear platinum-based compounds (that contain alkane bridging linkers of eight, ten and twelve carbon atoms in length) were characterised to assess their potential as anticancer agents. METHODS: The properties of these compounds were determined using a DNA template containing seven tandem telomeric repeat sequences. A linear amplification reaction was used in combination with capillary electrophoresis to quantify the sequence specificity of DNA adducts formed by these compounds at base pair resolution. The DNA cross-linking ability of these compounds was assessed using denaturing agarose gel electrophoresis and cytotoxicity was determined in HeLa cells using a colorimetric cell viability assay. RESULTS: The dinuclear compounds were found to preferentially form DNA adducts at guanine bases and they exhibited different damage intensity profiles at the telomeric repeat sequences compared to that of cisplatin. The dinuclear compounds were found to exhibit a low level of cytotoxicity relative to cisplatin and their cytotoxicity increased as the linker length increased. Conversely, the interstrand cross-linking efficiency of the dinuclear compounds increased as the linker length decreased and the compound with the shortest alkane linker was six-fold more effective than cisplatin. CONCLUSIONS: Since the bifunctional compounds exhibit variation in sequence specificity of adduct formation and a greater ability to cross-link DNA relative to cisplatin they warrant further investigation towards the goal of developing new cancer chemotherapeutic agents.
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Johnson et al. (2016) studied Cervical cancer (in vitro). Novel dinuclear platinum-based compounds (1,8 platinum, 1,10 platinum, 1,12 platinum) vs. Cisplatin and transplatin was evaluated on Interstrand cross-linking efficiency (ICLE) and cytotoxicity (IC50). The novel dinuclear platinum compounds exhibited greater interstrand DNA cross-linking efficiency than cisplatin, with the 1,8 platinum compound being six-fold more effective, though they demonstrated lower cytotoxicity in HeLa cells.
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