Department of Surgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Translational Cancer Medicine Research Program, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
PLoS One. 2019 Jul 17;14(7):e0219245. doi: 10.1371/journal.pone.0219245. eCollection 2019.
The link between inflammation and carcinogenesis is indisputable. In trying to understand key factors at play, cancer research has developed an interest in the toll-like receptors (TLRs), which have shown signs of having prognostic value in various adenocarcinomas. We began investigating the expression of toll-like receptors 1, 3, 5, 7, and 9 to evaluate their prognostic value of patients with pancreatic ductal adenocarcinoma (PDAC).
We collected tumor biopsies from 154 stage I-III PDAC patients surgically treated at Helsinki University Hospital between 2002 and 2011, excluding patients undergoing neoadjuvant therapy. We used tissue microarray slides and immunohistochemistry to assess expression of TLRs 1, 3, 5, 7, and 9 in PDAC tissue. Immunopositivity scores and clinicopathological characteristics were subjected to Fisher's exact test or the linear-by-linear association test. For the survival analysis, we applied the Kaplan-Meier method and log-rank test, and the Cox regression proportional hazard model served for univariate and multivariate analyses.
Strong TLR1 expression was observable in 60 (39%), strong TLR3 in 48 (31%), strong TLR5 in 58 (38%), strong TLR7 in 14 (9%), and strong TLR9 in 22 (14%) patients. The multivariate analysis showed strong TLR1 expression to associate with better survival than moderate, low, or negative expression (HR = 0.68; 95% CI 0.47-0.99; p = 0.044). Additionally, those few patients with tumors negative for TLR1, TLR3, TLR7, or TLR9 fared poorly (HR = 2.41; 95% CI 1.31-4.43; p = 0.005; n = 13).
Strong TLR1 expression suggested better prognosis in PDAC patients, whereas negative expression of TLR1, TLR3, TLR7, or TLR9 was a sign of poor prognosis.
炎症与癌变之间的联系是无可争议的。在试图了解起关键作用的因素时,癌症研究对 Toll 样受体(TLRs)产生了兴趣,这些受体在各种腺癌中表现出具有预后价值的迹象。我们开始研究 Toll 样受体 1、3、5、7 和 9 的表达,以评估其对胰腺导管腺癌(PDAC)患者的预后价值。
我们收集了 2002 年至 2011 年间在赫尔辛基大学医院接受手术治疗的 154 例 I-III 期 PDAC 患者的肿瘤活检,排除接受新辅助治疗的患者。我们使用组织微阵列载玻片和免疫组织化学方法评估 PDAC 组织中 TLRs 1、3、5、7 和 9 的表达。免疫阳性评分和临床病理特征采用 Fisher 确切检验或线性关联检验。对于生存分析,我们应用 Kaplan-Meier 方法和对数秩检验,Cox 回归比例风险模型用于单变量和多变量分析。
在 60 例(39%)患者中观察到 TLR1 表达强阳性,48 例(31%)患者 TLR3 表达强阳性,58 例(38%)患者 TLR5 表达强阳性,14 例(9%)患者 TLR7 表达强阳性,22 例(14%)患者 TLR9 表达强阳性。多变量分析显示,与中度、低度或阴性表达相比,TLR1 表达强阳性与更好的生存相关(HR = 0.68;95%CI 0.47-0.99;p = 0.044)。此外,那些 TLR1、TLR3、TLR7 或 TLR9 阴性的少数患者预后不良(HR = 2.41;95%CI 1.31-4.43;p = 0.005;n = 13)。
TLR1 表达强阳性提示 PDAC 患者预后较好,而 TLR1、TLR3、TLR7 或 TLR9 表达阴性则提示预后不良。