Teper Yaroslav, Eibl Guido
Department of Surgery, David Geffen School of Medicine at UCLA, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Cancers (Basel). 2020 Jul 17;12(7):1946. doi: 10.3390/cancers12071946.
Obesity is a known risk factor for the development of pancreatic cancer, one of the deadliest types of malignancies. In recent years it has become clear that the pancreatic microenvironment is critically involved and a contributing factor in accelerating pancreatic neoplasia. In this context obesity-associated chronic inflammation plays an important role. Among several immune cells, macrophages have been shown to contribute to obesity-induced tissue inflammation. This review article summarizes the current knowledge about the role of pancreatic macrophages in early pancreatic cancer development. It describes the heterogenous origin and mixture of pancreatic macrophages, their role in pancreatic endocrine and exocrine pathology, and the impact of obesity on islet and stromal macrophages. A model is postulated, by which during obesity monocytes are recruited into the pancreas, where they are polarized into pro-inflammatory macrophages that drive early pancreatic neoplasia. This occurs in the presence of local inflammatory, metabolic, and endocrine signals. A stronger appreciation and more detailed knowledge about the role of macrophages in early pancreatic cancer development will lead to innovative preventive or interceptive strategies.
肥胖是已知的胰腺癌发生风险因素,胰腺癌是最致命的恶性肿瘤类型之一。近年来,已明确胰腺微环境在加速胰腺肿瘤形成过程中起关键作用且是一个促成因素。在这种情况下,肥胖相关的慢性炎症起着重要作用。在几种免疫细胞中,巨噬细胞已被证明会导致肥胖诱导的组织炎症。这篇综述文章总结了目前关于胰腺巨噬细胞在早期胰腺癌发展中作用的知识。它描述了胰腺巨噬细胞的异源起源和混合情况、它们在胰腺内分泌和外分泌病理学中的作用,以及肥胖对胰岛和基质巨噬细胞的影响。提出了一个模型,在肥胖期间,单核细胞被招募到胰腺中,在那里它们被极化为促炎性巨噬细胞,从而驱动早期胰腺肿瘤形成。这发生在局部炎症、代谢和内分泌信号存在的情况下。对巨噬细胞在早期胰腺癌发展中作用的更深入理解和更详细认识将带来创新的预防或拦截策略。