Ahmad Munirah, Suhaimi Shazlan-Noor, Chu Tai-Lin, Abdul Aziz Norazlin, Mohd Kornain Noor-Kaslina, Samiulla D S, Lo Kwok-Wai, Ng Chew-Hee, Khoo Alan Soo-Beng
Molecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Kuala Lumpur, Malaysia.
Department of Pathology, Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh, Selangor, Malaysia.
PLoS One. 2018 Jan 12;13(1):e0191295. doi: 10.1371/journal.pone.0191295. eCollection 2018.
Copper(II) ternary complex, [Cu(phen)(C-dmg)(H2O)]NO3 was evaluated against a panel of cell lines, tested for in vivo efficacy in nasopharyngeal carcinoma xenograft models as well as for toxicity in NOD scid gamma mice. The Cu(II) complex displayed broad spectrum cytotoxicity against multiple cancer types, including lung, colon, central nervous system, melanoma, ovarian, and prostate cancer cell lines in the NCI-60 panel. The Cu(II) complex did not cause significant induction of cytochrome P450 (CYP) 3A and 1A enzymes but moderately inhibited CYP isoforms 1A2, 2C9, 2C19, 2D6, 2B6, 2C8 and 3A4. The complex significantly inhibited tumor growth in nasopharyngeal carcinoma xenograft bearing mice models at doses which were well tolerated without causing significant or permanent toxic side effects. However, higher doses which resulted in better inhibition of tumor growth also resulted in toxicity.
对铜(II)三元配合物[Cu(phen)(C-dmg)(H₂O)]NO₃针对一组细胞系进行了评估,并在鼻咽癌异种移植模型中测试了其体内疗效以及在NOD scid gamma小鼠中的毒性。该铜(II)配合物对多种癌症类型表现出广谱细胞毒性,包括NCI-60细胞系面板中的肺癌、结肠癌、中枢神经系统癌、黑色素瘤、卵巢癌和前列腺癌细胞系。该铜(II)配合物不会显著诱导细胞色素P450(CYP)3A和1A酶,但会适度抑制CYP同工酶1A2、2C9、2C19、2D6、2B6、2C8和3A4。在耐受性良好且未引起显著或永久性毒副作用的剂量下,该配合物显著抑制了携带鼻咽癌异种移植瘤小鼠模型中的肿瘤生长。然而,导致更好肿瘤生长抑制效果的更高剂量也会产生毒性。