The Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
Br J Cancer. 2013 Mar 19;108(5):997-1003. doi: 10.1038/bjc.2013.24. Epub 2013 Feb 5.
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy associated with <5% 5-year survival, in which standard chemotherapeutics have limited benefit. The disease is associated with significant intra- and peritumoral inflammation and failure of protective immunosurveillance. Indeed, inflammatory signals are implicated in both tumour initiation and tumour progression. The major pathways regulating PDAC-associated inflammation are now being explored. Activation of leukocytes, and upregulation of cytokine and chemokine signalling pathways, both have been shown to modulate PDAC progression. Therefore, targeting inflammatory pathways may be of benefit as part of a multi-target approach to PDAC therapy. This review explores the pathways known to modulate inflammation at different stages of tumour development, drawing conclusions on their potential as therapeutic targets in PDAC.
胰腺导管腺癌 (PDAC) 是一种侵袭性恶性肿瘤,其 5 年生存率 <5%,标准化疗的获益有限。该疾病与显著的肿瘤内和肿瘤周围炎症以及保护性免疫监视失败有关。事实上,炎症信号与肿瘤的发生和肿瘤的进展都有关。目前正在探索调控 PDAC 相关炎症的主要途径。白细胞的激活以及细胞因子和趋化因子信号通路的上调都已被证明可以调节 PDAC 的进展。因此,作为 PDAC 治疗多靶点方法的一部分,靶向炎症途径可能有益。本文综述了已知在肿瘤发展的不同阶段调节炎症的途径,并就其作为 PDAC 治疗靶点的潜力得出结论。