Department of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", Bari, Italy.
Department of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", Bari, Italy,
Neuroendocrinology. 2019;109(2):83-99. doi: 10.1159/000497355. Epub 2019 Jan 30.
Neuroendocrine tumors (NETs) include a heterogeneous group of malignancies arising in the diffuse neuroendocrine system and characterized by indolent growth. Complex interactions take place among the cellular components of the microenvironment of these tumors, and the recognition of the molecular mediators of their interplay and cross talk is crucial to discover novel therapeutic targets. NET cells overexpress a plethora of proangiogenic molecules including vascular endothelial growth factor, platelet-derived growth factor, fibroblast growth factor, semaphorins, and angiopoietins that promote both recruitment and proliferation of endothelial cell precursors, thus resulting among the most vascularized cancers with a microvessel density 10-fold higher than epithelial tumors. Also, NETs operate multifaceted interactions with stromal cells, both at local and distant sites, and whether their paracrine secretion of serotonin, connective tissue growth factor, and transforming growth factor β primarily drives the fibroblast activation to enhance the tumor proliferation, on the other side NET-derived profibrotic factors accelerate the extracellular matrix remodeling and contribute to heart valves and/or mesenteric fibrosis development, namely, major complications of functioning NETs. However, at present, little is known on the immune landscape of NETs, but accumulating evidence shows that tumor-infiltrating neutrophils, mast cells, and/or macrophages concur to promote the neoangiogenic switch of these tumors by either direct or indirect mechanisms. On the other hand, immune checkpoint molecules are heterogeneously expressed in NETs' surrounding cells, and it is unclear whether or not tumor-infiltrating lymphocytes are antitumor armed within the microenvironment, given their low mutational load. Here, we review the current knowledge on both gastroenteropancreatic and pulmonary NETs' microenvironment as well as both established and innovative treatments aimed at targeting the tumor-host interplay.
神经内分泌肿瘤(NET)包括一组起源于弥散神经内分泌系统的异质性恶性肿瘤,其生长缓慢。这些肿瘤的微环境中的细胞成分之间存在复杂的相互作用,识别它们相互作用和串扰的分子介质对于发现新的治疗靶点至关重要。NET 细胞过度表达多种促血管生成分子,包括血管内皮生长因子、血小板衍生生长因子、成纤维细胞生长因子、信号素和血管生成素,这些分子促进内皮细胞前体的募集和增殖,因此成为血管化程度最高的癌症之一,其微血管密度比上皮肿瘤高 10 倍。此外,NET 与基质细胞在局部和远处都进行多方面的相互作用,它们的分泌的 5-羟色胺、结缔组织生长因子和转化生长因子β是否主要驱动成纤维细胞的激活,以增强肿瘤的增殖,另一方面,NET 衍生的促纤维化因子加速细胞外基质重塑,并导致心脏瓣膜和/或肠系膜纤维化的发展,即功能性 NET 的主要并发症。然而,目前对 NET 的免疫景观知之甚少,但越来越多的证据表明,肿瘤浸润的中性粒细胞、肥大细胞和/或巨噬细胞通过直接或间接机制共同促进这些肿瘤的新生血管形成开关。另一方面,免疫检查点分子在 NET 周围细胞中呈异质表达,尚不清楚肿瘤浸润的淋巴细胞是否在微环境中具有抗肿瘤武装,因为它们的突变负荷较低。在这里,我们回顾了胃肠道胰腺和肺部 NET 微环境的最新知识,以及针对靶向肿瘤-宿主相互作用的既定和创新治疗方法。