Huang Yide, Zhang Shu-Dong, McCrudden Cian, Chan Kwok-Wah, Lin Yao, Kwok Hang-Fai
College of Life Sciences, Fujian Normal University, Fuzhou, Fujian, P.R. China.
Center for Cancer Research and Cell Biology and School of Pharmacy, Queen's University Belfast, Belfast, Northern Ireland, UK.
Oncol Rep. 2015 Jun;33(6):3075-84. doi: 10.3892/or.2015.3933. Epub 2015 Apr 27.
Immunotherapy is a promising strategy for the treatment of various types of cancer. An antibody that targets programmed death ligand-1 (PD-L1) pathway has been shown to be active towards various types of cancer, including melanoma and lung cancer. MPDL3280A, an anti-PD-L1 antibody, has shown clear clinical activity in PD-L1-overexpressing bladder cancer with an objective response rate of 40-50%, resulting in a breakthrough therapy designation granted by FDA. These events pronounce the importance of targeting the PD-L1 pathway in the treatment of bladder cancer. In the present study, we investigated the prognostic significance of the expression of three genes in the PD-L1 pathway, including PD-L1, B7.1 and PD-1, in three independent bladder cancer datasets in the Gene Expression Omnibus database. PD-L1, B7.1 and PD-1 were significantly associated with clinicopathological parameters indicative of a more aggressive phenotype of bladder cancer, such as a more advanced stage and a higher tumor grade. In addition, a high level expression of PD-L1 was associated with reduced patient survival. Of note, the combination of PD-L1 and B7.1 expression, but not other combinations of the three genes, were also able to predict patient survival. Our findings support the development of anti-PD-L1, which blocks PD-L1-PD-1 and B7.1-PD-L1 interactions, in treatment of bladder cancer. The observations were consistent in the three independent bladder cancer datasets consisting of a total of 695 human bladder specimens. The datasets were then assessed and it was found that the expression levels of the chemokine CC-motif ligand (CCL), CCL3, CCL8 and CCL18, were correlated with the PD-L1 expression level, while ADAMTS13 was differentially expressed in patients with a different survival status (alive or deceased). Additional investigations are required to elucidate the role of these genes in the PD-L1-mediated immune system suppression and bladder cancer progression. In conclusion, findings of this study suggested that PD-L1 is an important prognostic marker and a therapeutic target for bladder cancer.
免疫疗法是治疗各类癌症的一种很有前景的策略。一种靶向程序性死亡配体-1(PD-L1)通路的抗体已被证明对包括黑色素瘤和肺癌在内的各类癌症有效。抗PD-L1抗体MPDL3280A在PD-L1过表达的膀胱癌中显示出明显的临床活性,客观缓解率为40%-50%,因此获得了美国食品药品监督管理局(FDA)授予的突破性疗法认定。这些事件表明在膀胱癌治疗中靶向PD-L1通路的重要性。在本研究中,我们在基因表达综合数据库中的三个独立膀胱癌数据集中,研究了PD-L1通路中三个基因(包括PD-L1、B7.1和PD-1)表达的预后意义。PD-L1、B7.1和PD-1与指示膀胱癌更具侵袭性表型的临床病理参数显著相关,如更晚期别和更高肿瘤分级。此外,PD-L1的高表达与患者生存率降低相关。值得注意的是,PD-L1和B7.1表达的组合,而非这三个基因的其他组合,也能够预测患者生存率。我们的研究结果支持开发抗PD-L1药物,其可阻断PD-L1-PD-1和B7.1-PD-L1相互作用,用于治疗膀胱癌。在总共包含695个人类膀胱标本的三个独立膀胱癌数据集中,这些观察结果是一致的。然后对这些数据集进行评估,发现趋化因子CC基序配体(CCL)、CCL3、CCL8和CCL18的表达水平与PD-L1表达水平相关,而ADAMTS13在不同生存状态(存活或死亡)的患者中差异表达。需要进一步研究以阐明这些基因在PD-L1介导的免疫系统抑制和膀胱癌进展中的作用。总之,本研究结果表明PD-L1是膀胱癌的一个重要预后标志物和治疗靶点。