BioChemLab, Department of Pharmacy, School of Medicine and Surgery, University of Naples "Federico II", Via D. Montesano 49, 80131 Napoli, Italy.
Biogem Scarl, Institute of Genetic Research, Laboratory of Molecular and Precision Oncology, 83031 Ariano Irpino, Italy.
Int J Mol Sci. 2023 Mar 30;24(7):6473. doi: 10.3390/ijms24076473.
Based on compelling preclinical evidence concerning the progress of our novel ruthenium-based metallotherapeutics, we are focusing research efforts on challenging indications for the treatment of invasive neoplasms such as the triple-negative breast cancer (TNBC). This malignancy mainly afflicts younger women, who are black, or who have a BRCA1 mutation. Because of faster growing and spreading, TNBC differs from other invasive breast cancers having fewer treatment options and worse prognosis, where existing therapies are mostly ineffective, resulting in a large unmet biomedical need. In this context, we benefited from an experimental model of TNBC both in vitro and in vivo to explore the effects of a biocompatible cationic liposomal nanoformulation, named HoThyRu/DOTAP, able to effectively deliver the antiproliferative ruthenium(III) complex AziRu, thus resulting in a prospective candidate drug. As part of the multitargeting mechanisms featuring metal-based therapeutics other than platinum-containing agents, we herein validate the potential of HoThyRu/DOTAP liposomes to act as a multimodal anticancer agent through inhibition of TNBC cell growth and proliferation, as well as migration and invasion. The here-obtained preclinical findings suggest a potential targeting of the complex pathways network controlling invasive and migratory cancer phenotypes. Overall, in the field of alternative chemotherapy to platinum-based drugs, these outcomes suggest prospective brand-new settings for the nanostructured AziRu complex to get promising goals for the treatment of metastatic TNBC.
基于我们新型钌基金属疗法进展的令人信服的临床前证据,我们正在集中研究努力,以挑战治疗侵袭性肿瘤的适应症,如三阴性乳腺癌(TNBC)。这种恶性肿瘤主要影响年轻的女性,她们是黑人,或有 BRCA1 突变。由于生长和扩散更快,TNBC 与其他侵袭性乳腺癌不同,治疗选择较少,预后较差,现有疗法大多无效,因此存在巨大的未满足的生物医学需求。在这种情况下,我们受益于 TNBC 的体外和体内实验模型,以探索一种名为 HoThyRu/DOTAP 的生物相容性阳离子脂质体纳米制剂对有效传递抗增殖钌(III)配合物 AziRu 的影响,从而成为一种有前景的候选药物。作为除含铂剂以外的金属疗法的多靶向机制的一部分,我们在此验证了 HoThyRu/DOTAP 脂质体作为多模式抗癌剂的潜力,通过抑制 TNBC 细胞的生长和增殖以及迁移和侵袭。这里获得的临床前发现表明,复杂的通路网络可能成为控制侵袭性和迁移性癌症表型的潜在靶点。总的来说,在替代铂类药物的化疗领域,这些结果为纳米结构的 AziRu 配合物提供了有前途的新应用前景,有望实现转移性 TNBC 的治疗目标。