Pd(II) and Pt(II) Trinuclear Chelates with Spermidine: Selective Anticancer Activity towards TNBC-Sensitive and -Resistant to Cisplatin

Triple-negative breast cancer (TNBC) is one of the most aggressive forms of breast cancer and constitutes 10-20% of all breast cancer cases. Even though platinum-based drugs such as cisplatin and carboplatin are effective in TNBC patients, their toxicity and development of cancer drug resistance often hamper their clinical use. Hence, novel drug entities with improved tolerability and selectivity profiles, as well as the ability to surpass resistance, are needed. The current study focuses on Pd(II) and Pt(II) trinuclear chelates with spermidine (Pd(3)Spd(2) and Pt(3)Spd(2)) for evaluating their antineoplastic activity having been assessed towards (i) cisplatin-resistant TNBC cells (MDA-MB-231/R), (ii) cisplatin-sensitive TNBC cells (MDA-MB-231) and (iii) non-cancerous human breast cells (MCF-12A, to assess the cancer selectivity/selectivity index). Additionally, the complexes' ability to overcome acquired resistance (resistance index) was determined. This study revealed that Pd(3)Spd(2) activity greatly exceeds that displayed by its Pt analog. In addition, Pd(3)Spd(2) evidenced a similar antiproliferative activity in both sensitive and resistant TNBC cells (IC50 values 4.65-8.99 mu M and 9.24-13.34 mu M, respectively), with a resistance index lower than 2.3. Moreover, this Pd compound showed a promising selectivity index ratio: >6.28 for MDA-MB-231 cells and >4.59 for MDA-MB-231/R cells. Altogether, the data presently gathered reveal Pd(3)Spd(2) as a new, promising metal-based anticancer agent, which should be further explored for the treatment of TNBC and its cisplatin-resistant forms.

Automated summary

Triple-negative breast cancer (TNBC) is a highly aggressive form of breast cancer and current drug treatments often face limitations. In this study, Pd(3)Spd(2) was found to be a promising metal-based anticancer agent for TNBC treatment, surpassing its Pt analog in activity. Pd(3)Spd(2) demonstrated similar antiproliferative activity in both sensitive and resistant TNBC cells and showed a promising selectivity index ratio, indicating its potential for further exploration in treating TNBC and its cisplatin-resistant forms.