Department of Medical and Surgical Sciences, Clinical Surgery Unit, University "Magna Graecia" Medical School, Viale Europa, Germaneto, 88100 Catanzaro, Italy.
Interventional Oncology Unit with Integrated Section of Translational Medical Oncology National Cancer Research Centre, Istituto Tumori "Giovanni Paolo II", viale Orazio Flacco 65, 70124 Bari, Italy.
Int J Mol Sci. 2018 Apr 12;19(4):1176. doi: 10.3390/ijms19041176.
Mast cells and macrophages can play a role in tumor angiogenesis by stimulating microvascular density (MVD). The density of mast cells positive to tryptase (MCDPT), tumor-associated macrophages (TAMs), and MVD were evaluated in a series of 86 gastric cancer (GC) tissue samples from patients who had undergone potential curative surgery. MCDPT, TAMs, and MVD were assessed in tumor tissue (TT) and in adjacent normal tissue (ANT) by immunohistochemistry and image analysis. Each of the above parameters was correlated with the others and, in particular for TT, with important clinico-pathological features. In TT, a significant correlation between MCDPT, TAMs, and MVD was found by Pearson -test analysis ( ranged from 0.01 to 0.02). No correlation to the clinico-pathological features was found. A significant difference in terms of mean MCDPT, TAMs, and MVD between TT and ANT was found ( ranged from 0.001 to 0.002). Obtained data suggest MCDPT, TAMs, and MVD increased from ANT to TT. Interestingly, MCDPT and TAMs are linked in the tumor microenvironment and they play a role in GC angiogenesis in a synergistic manner. The assessment of the combination of MCDPT and TAMs could represent a surrogate marker of angiogenesis and could be evaluated as a target of novel anti-angiogenic therapies in GC patients.
肥大细胞和巨噬细胞可以通过刺激微血管密度(MVD)在肿瘤血管生成中发挥作用。在一系列 86 例接受潜在根治性手术的胃癌(GC)患者的组织样本中,评估了对胰蛋白酶阳性的肥大细胞(MCDPT)、肿瘤相关巨噬细胞(TAMs)和 MVD 的密度。通过免疫组织化学和图像分析评估 MCDPT、TAMs 和 MVD 在肿瘤组织(TT)和相邻正常组织(ANT)中的表达。评估了上述每个参数与其他参数的相关性,特别是对于 TT,还评估了其与重要临床病理特征的相关性。在 TT 中,Pearson 检验分析发现 MCDPT、TAMs 和 MVD 之间存在显著相关性(范围为 0.01 至 0.02)。与临床病理特征无相关性。在 TT 和 ANT 之间,MCDPT、TAMs 和 MVD 的平均值存在显著差异(范围为 0.001 至 0.002)。研究数据表明,从 ANT 到 TT,MCDPT、TAMs 和 MVD 逐渐增加。有趣的是,MCDPT 和 TAMs 在肿瘤微环境中相互关联,并以协同方式发挥作用,促进 GC 血管生成。评估 MCDPT 和 TAMs 的组合可能代表血管生成的替代标志物,并可作为 GC 患者新型抗血管生成治疗的靶点进行评估。