Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur, 50603, Malaysia; Aurigene Discovery Technologies, IPPP, University Malaya, Kuala Lumpur, 50603, Malaysia.
Aurigene Discovery Technologies Limited, Electronic City, Bangalore, 560100, Karnataka, India.
Biomed Pharmacother. 2019 Feb;110:29-36. doi: 10.1016/j.biopha.2018.11.010. Epub 2018 Nov 17.
Malignant melanoma continues to be a fatal disease for which novel and long-term curative breakthroughs are desired. One such innovative idea would be to assess combination therapeutic treatments - by way of combining two potentially effective and very different therapy. Previously, we have shown that DHODH inhibitors, A771726 and Brequinar sodium (BQR) induced cell growth impairment in melanoma cells. Similar results were seen with DHODH RNA interference (shRNA). In the present study, we showed that combination of BQR with doxorubicin resulted in synergistic and additive cell growth inhibition in these cells. In addition, in vivo studies with this combination of drugs demonstrated an almost 90% tumor regression in nude mice bearing melanoma tumors. Cell cycle regulatory proteins, cyclin B and its binding partner pcdc-2 and p21 were significantly downregulated and upregulated respectively following the combined treatment. Given that we have observed synergistic effects with BQR and doxorubicin, both in vitro and in vivo, these drugs potentially represent a new combination in the targeted therapy of melanoma.
恶性黑色素瘤仍然是一种致命的疾病,人们希望能有新的、长期的治疗突破。一个这样的创新想法是评估联合治疗方法 - 通过结合两种潜在有效且非常不同的治疗方法。此前,我们已经表明,DHODH 抑制剂 A771726 和 Brequinar 钠(BQR)可抑制黑色素瘤细胞的细胞生长。DHODH RNA 干扰(shRNA)也出现了类似的结果。在本研究中,我们表明 BQR 与阿霉素联合使用可协同抑制这些细胞的细胞生长。此外,用该药物组合进行的体内研究表明,在携带黑色素瘤肿瘤的裸鼠中,肿瘤几乎消退了 90%。细胞周期调节蛋白 cyclin B 及其结合伴侣 pcdc-2 和 p21 在联合治疗后分别显著下调和上调。鉴于我们在体外和体内都观察到 BQR 和阿霉素具有协同作用,这些药物可能代表黑色素瘤靶向治疗的一种新联合用药。