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Inflammation and cancer: Till death tears them apart

机译:炎症和癌症:直到死亡将它们撕裂

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摘要

Advances in biotechnology have enabled the collection of an immeasurable amount of information from genomic, transcriptomic, metabolomic and proteomic studies of tumours within their microenvironments. The dissection of cytokine and chemokine networks has provided new clues to the interactions between cancer cells and their surrounding inflammatory landscape. To bridge the gap between chronic inflammation and cancer, dynamic participants in the tumour microenvironment have been identified, including tumour-associated macrophages (TAMs) and regulatory T cells (Tregs). Both of these cell types are notable for their ability to cause immunosuppressive conditions and support the evasion of tumour immune surveillance. It is clear now that the tumour-promoting inflammatory environment has to be included as one of the major cancer hallmarks. This review explores the recent advances in the understanding of cancer-related inflammation and how this is being applied to comparative oncology studies in humans and domestic species, such as the dog. (C) 2015 Elsevier Ltd. All rights reserved.
机译:生物技术的进步使得能够从其微环境内肿瘤的基因组,转录组学,代谢组学和蛋白质组学研究中收集到不可估量的信息。细胞因子和趋化因子网络的解剖为癌细胞及其周围炎症区域之间的相互作用提供了新的线索。为了弥合慢性炎症和癌症之间的鸿沟,已经确定了肿瘤微环境中的动态参与者,包括肿瘤相关巨噬细胞(TAM)和调节性T细胞(Treg)。这两种细胞类型均具有引起免疫抑制条件并支持逃避肿瘤免疫监视的能力。现在很明显,必须将促进肿瘤的炎症环境作为主要的癌症标志之一。这篇综述探索了对癌症相关炎症的理解的最新进展,以及如何将其应用于人类和家养物种(如狗)的比较肿瘤学研究。 (C)2015 Elsevier Ltd.保留所有权利。

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