posted on 2019-06-05, 09:08authored byPaul B. Cressey, Arvin Eskandari, Kogularamanan Suntharalingam
Cancer stem cells (CSCs) are thought to be responsible for cancer relapse. CSCs are a subtype of cancer cells with the ability to differentiate, self-renew, and form secondary or tertiary tumors. Current cancer treatments—including chemotherapy, radiation, and surgery—effectively remove bulk cancer cells but are unable to eliminate CSCs. Here, we present the synthesis, characterization, and anti-CSC properties of a cobalt(III)–cyclam complex bearing two tolfenamic acid moieties, 3. Notably, 3 displays sub-micromolar potency towards breast CSCs and bulk breast cancer cells. Detailed mechanistic studies show that 3 is taken up readily by breast CSCs, enters the nucleus, causes DNA damage, and induces caspase-dependent apoptosis. Furthermore, 3 inhibits cyclooxygenase-2 (COX-2) expression in CSCs. The mechanism of action of 3 is similar to that of a naproxen-appended cobalt(III)–cyclam complex, 1 recently reported by our group. The advantage of 3 over 1 is that it has the potential to remove whole tumor populations (bulk cancer cells and CSCs) with a single dose.
Funding
Kogularamanan Suntharalingam is supported by an Early Career Fellowship (ECF-2014-178)
from the Leverhulme Trust. Arvin Eskandari received financial support from a King’s College London Faculty
Graduate School International Studentship. We are grateful to Robert Weinberg for providing the HMLER and
HMLER-shEcad cell lines used in this study
History
Citation
Inorganics, 2017, 5 (1), 12
Author affiliation
/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry