Department of Surgery, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
Department of Pathology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
PLoS One. 2022 May 10;17(5):e0267792. doi: 10.1371/journal.pone.0267792. eCollection 2022.
Toll-like receptors (TLRs) play a pivotal role in the immune system and carcinogenesis. There is no research on TLR expression and association with survival among preoperatively treated pancreatic cancer patients. We studied the expression intensity and prognostic value of TLRs in pancreatic cancer patients treated with neoadjuvant therapy (NAT) and compared the results to patients undergoing upfront surgery (US).
Between 2000 and 2015, 71 borderline resectable patients were treated with NAT and surgery and 145 resectable patients underwent upfront surgery at Helsinki University Hospital, Finland. We immunostained TLRs 1-5, 7, and 9 on sections of tissue-microarray. We classified TLR expression as 0 (negative), 1 (mild), 2 (moderate), or 3 (strong) and divided into high (2-3) and low (0-1) expression for statistical purposes.
Among TLRs 1, 3, and 9 (TLR1 81% vs 70%, p = 0.008; TLR3 92% vs 68%, p = 0.001; TLR9 cytoplasmic 83% vs 42%, p<0.001; TLR9 membranous 53% vs 25%, p = 0.002) NAT patients exhibited a higher immunopositivity score more frequently than patients undergoing upfront surgery. Among NAT patients, a high expression of TLR1 [Hazards ratio (HR) 0.48, p<0.05] associated with a longer postoperative survival, whereas among US patients, high expression of TLR5 (HR 0.64, p<0.05), TLR7 (HR 0.59, p<0.01, and both TLR7 and TLR9 (HR 0.5, p<0.01) predicted a favorable postoperative outcome in separate analysis adjusted for background variables.
We found higher immunopositive intensities among TLRs 1, 3, and 9 in NAT patients. A high TLR1 expression associated with a longer survival among NAT patients, however, among US patients, high expression intensity of TLR5 and TLR7 predicted a favorable postoperative outcome in the adjusted analysis.
Toll 样受体 (TLR) 在免疫系统和癌变中起着关键作用。目前还没有关于 TLR 表达与接受新辅助治疗 (NAT) 的胰腺癌患者生存情况之间关系的研究。我们研究了 TLR 在接受新辅助治疗的胰腺癌患者中的表达强度及其预后价值,并将结果与接受直接手术 (US) 的患者进行了比较。
在 2000 年至 2015 年间,芬兰赫尔辛基大学医院对 71 名边界可切除的患者进行了 NAT 和手术治疗,对 145 名可切除的患者进行了直接手术。我们对组织微阵列的组织切片进行了 TLR1-5、7 和 9 的免疫染色。我们将 TLR 表达分类为 0(阴性)、1(轻度)、2(中度)或 3(强),并为了统计目的将其分为高(2-3)和低(0-1)表达。
在 TLR1、3 和 9 中(TLR1 为 81%对 70%,p=0.008;TLR3 为 92%对 68%,p=0.001;TLR9 细胞质为 83%对 42%,p<0.001;TLR9 膜性为 53%对 25%,p=0.002),接受 NAT 的患者比直接手术的患者更频繁地表现出更高的免疫阳性评分。在接受 NAT 的患者中,TLR1 的高表达[风险比 (HR) 0.48,p<0.05]与术后生存时间延长相关,而在直接手术的患者中,TLR5(HR 0.64,p<0.05)、TLR7(HR 0.59,p<0.01)和 TLR7 与 TLR9(HR 0.5,p<0.01)的高表达均预测了术后结局良好,这在调整背景变量后的单独分析中得到了证实。
我们发现 TLR1、3 和 9 在接受 NAT 的患者中的免疫阳性强度更高。TLR1 表达高与接受 NAT 的患者的生存时间延长相关,而在直接手术的患者中,TLR5 和 TLR7 的高表达强度在调整后的分析中预测了术后良好的结局。