Xiang Benedict Lian Shi, Kwok-Wai Lo, Soo-Beng Alan Khoo, Mohana-Kumaran Nethia
School of Biological Sciences, Universiti Sains Malaysia, 11800 USM Pulau Pinang, Malaysia.
Department of Anatomical and Cellular Pathology and State Key Laboratory in Oncology in South China, The Chinese University of Hong Kong, Central Ave, Hong Kong.
Trop Life Sci Res. 2020 Oct;31(3):1-13. doi: 10.21315/tlsr2020.31.3.1. Epub 2020 Oct 15.
The BCL-2 anti-apoptotic proteins are over-expressed in many cancers and hence are attractive therapeutic targets. In this study, we tested the sensitivity of two Nasopharyngeal Carcinoma (NPC) cell lines HK1 and C666-1 to Maritoclax, which is reported to repress anti-apoptotic protein MCL-1 and BH3 mimetic ABT-263, which selectively inhibits anti-apoptotic proteins BCL-2, BCL-XL and BCL-w. We investigated the sensitisation of the NPC cell lines to these drugs using the SYBR Green I assay and 3D NPC spheroids. We report that Maritoclax repressed anti-apoptotic proteins MCL-1, BCL-2, and BCL-XL in a dose- and time-dependent manner and displayed a single agent activity in inhibiting cell proliferation of the NPC cell lines. Moreover, combination of Maritoclax and ABT-263 exhibited synergistic antiproliferative effect in the HK1 cells. Similar results were obtained in the 3D spheroids generated from the HK1 cells. More notably, 3D HK1 spheroids either treated with single agent Maritoclax or combination with ABT-263, over 10 days, did not develop resistance to the treatment rapidly. Collectively, the findings illustrate that Maritoclax as a single agent or combination with BH3 mimetics could be potentially useful as treatment strategies for the management of NPC.
BCL-2抗凋亡蛋白在许多癌症中过度表达,因此是有吸引力的治疗靶点。在本研究中,我们测试了两种鼻咽癌(NPC)细胞系HK1和C666-1对Maritoclax的敏感性,据报道Maritoclax可抑制抗凋亡蛋白MCL-1,以及BH3模拟物ABT-263,后者可选择性抑制抗凋亡蛋白BCL-2、BCL-XL和BCL-w。我们使用SYBR Green I检测法和3D NPC球体研究了NPC细胞系对这些药物的敏感性。我们报告称,Maritoclax以剂量和时间依赖性方式抑制抗凋亡蛋白MCL-1、BCL-2和BCL-XL,并在抑制NPC细胞系的细胞增殖方面显示出单一药物活性。此外,Maritoclax和ABT-263联合使用在HK1细胞中表现出协同抗增殖作用。在由HK1细胞生成的3D球体中也获得了类似结果。更值得注意的是,用单一药物Maritoclax或与ABT-263联合处理的3D HK1球体在超过10天的时间里没有迅速产生耐药性。总的来说,这些发现表明,Maritoclax作为单一药物或与BH3模拟物联合使用可能是治疗NPC的潜在有用策略。