Second Department of Medical Oncology, Theagenion Cancer Hospital, 546 44 Thessaloniki, Greece.
Department of Basic Medical Sciences, Laboratory of Biology, School of Medicine, National and Kapodistrian University of Athens, 115 27 Athens, Greece.
Medicina (Kaunas). 2022 Oct 6;58(10):1399. doi: 10.3390/medicina58101399.
Background and Objectives: Triple-negative breast cancer (TNBC) is a highly heterogeneous subtype that is associated with unresponsiveness to therapy and hence with high mortality rates. In this study we aimed to investigate the prognostic role of the rs822336 G>C and rs822337 T>A polymorphisms of the PD-L1 (Programmed Death-Ligand 1) in TNBC patients. Materials and methods: Formalin-fixed paraffin-embedded tissues from 114 TNBC patients and blood samples from 124 healthy donors were genotyped, and subsequently extensive statistical analysis was performed in order to investigate the clinical value of these polymorphism in TNBC. Results: Regarding rs822336 G>C, we found that the CG genotype was the most common among women that harbored Stage IV breast tumors (81.8%; p = 0.022), recurred (38.9%; p = 0.02) and died (66.7%; p = 0.04). Similarly, the rs822337 T>A genotype AA is associated with worse prognosis, since it was the most common genotype among stage IV tumors (72.7%; p = 0.04) and in TNBC patients that relapsed (75%; p = 0.021) and died (81.5%; p = 0.004). Our statistical analysis revealed that the rs822336 G>C genotype CG and the rs822337 T>A allele AA are strongly associated with inferior DFS and OS intervals. Moreover, it was revealed that women harboring mutated genotypes of both SNPs had shorter disease-free (Kaplan−Meier; p = 0.037, Cox analysis; p = 0.04) and overall (Kaplan−Meier; p = 0.025, Cox analysis; p = 0.03) survival compared to patients having normal genotype of at least one SNP. Multivariate analysis also showed that the presence of mutated genotypes of both SNPs is a strong and independent marker for predicting shorter DFS (p = 0.02) and OS (p = 0.008). Conclusion: Our study revealed that PD-L1 rs822336 G>C and rs822337 T>A polymorphisms were differentially expressed in our cohort of TNBC patients, and that this distribution was associated with markers of unfavorable prognosis and worse survival.
三阴性乳腺癌(TNBC)是一种高度异质性的亚型,与治疗反应不佳有关,因此死亡率较高。本研究旨在探讨 PD-L1(程序性死亡配体 1)rs822336 G>C 和 rs822337 T>A 多态性在 TNBC 患者中的预后作用。
对 114 例 TNBC 患者的福尔马林固定石蜡包埋组织和 124 例健康供者的血样进行基因分型,随后进行广泛的统计分析,以探讨这些多态性在 TNBC 中的临床价值。
关于 rs822336 G>C,我们发现 CG 基因型在患有 IV 期乳腺癌的女性中最为常见(81.8%;p = 0.022),且易复发(38.9%;p = 0.02)和死亡(66.7%;p = 0.04)。同样,rs822337 T>A 基因型 AA 与较差的预后相关,因为它是 IV 期肿瘤中最常见的基因型(72.7%;p = 0.04),并且在复发(75%;p = 0.021)和死亡(81.5%;p = 0.004)的 TNBC 患者中也是如此。我们的统计分析显示,rs822336 G>C 基因型 CG 和 rs822337 T>A 等位基因 AA 与较差的无病生存期(DFS)和总生存期(OS)密切相关。此外,研究发现同时携带两个 SNP 突变基因型的女性无病生存期(Kaplan-Meier;p = 0.037,Cox 分析;p = 0.04)和总生存期(Kaplan-Meier;p = 0.025,Cox 分析;p = 0.03)均更短,与至少有一个 SNP 正常基因型的患者相比。多变量分析还表明,两个 SNP 突变基因型的存在是预测 DFS 更短(p = 0.02)和 OS 更短(p = 0.008)的有力且独立的标志物。
我们的研究表明,PD-L1 rs822336 G>C 和 rs822337 T>A 多态性在我们的 TNBC 患者队列中表达不同,且这种分布与预后不良和生存较差的标志物相关。