...
首页> 外文期刊>Oncology reports >Role of tumor-associated macrophages in the angiogenesis of well-differentiated hepatocellular carcinoma: Pathological-radiological correlation
【24h】

Role of tumor-associated macrophages in the angiogenesis of well-differentiated hepatocellular carcinoma: Pathological-radiological correlation

机译:肿瘤相关巨噬细胞在高分化肝细胞癌血管生成中的作用:病理-放射学相关性

获取原文
获取原文并翻译 | 示例
           

摘要

The role of tumor-associated macrophages (TAMs) in hepatocellular carcinoma (HCC) has not been fully investigated. The aim of the present study was to clarify whether TAMs are associated with the angiogenesis of HCC during its multistep development, especially at an early stage. Forty-three well-differentiated HCCs and 30 well- to moderately differentiated HCCs (nodule-in-nodule lesion) were used. We immunohistochemically assessed microvessel density (by CD34) and macrophage count (by CD68 or CD163). Computed tomography hepatic angiography (CTHA) was performed for 26 well-differentiated HCCs and all 30 well- to moderately differentiated HCCs. The pathological analysis of the 43 well-differentiated HCCs revealed a positive correlation between microvessel density and macrophage count (P=0.0026, r=0.4486). Based on the CTHA findings, 26 well-differentiated HCCs classified into a hyperattenuation group (n=14) and a hypo- or isoattenuation group (n=12). The microvessel density and macrophage count of the hyperattenuation group were significantly higher than those of the hypo- or isoattenuation group (P=0.0372 and P=0.0476). In the 30 well- to moderately differentiated HCCs, microvessel density of the moderately differentiated components was significantly higher than that of the well-differentiated components (P<0.0001). However, the macrophage count of the moderately differentiated component was significantly lower than that of the well-differentiated component (P<0.0001). All the moderately differentiated components showed marked hyperattenuation on CTHA. Tumor vascularity was correlated with macrophage count in the tumor when limited to well-differentiated HCCs. TAMs may have a role in promoting angiogenesis of HCC at an early stage during its multistep development.
机译:肿瘤相关巨噬细胞(TAM)在肝细胞癌(HCC)中的作用尚未得到充分研究。本研究的目的是弄清TAM是否与HCC的多步发育有关,尤其是在早期阶段。使用了43个高分化HCC和30个高分化至中分化HCC(结节内结节病灶)。我们通过免疫组化评估了微血管密度(通过CD34)和巨噬细胞计数(通过CD68或CD163)。对26例分化良好的HCC和所有30例中等至中等分化的HCC进行了计算机断层扫描肝血管造影(CTHA)。对43个分化良好的HCC的病理分析表明,微血管密度与巨噬细胞计数之间呈正相关(P = 0.0026,r = 0.4486)。根据CTHA的发现,将26个分化良好的HCC分为高衰减组(n = 14)和低衰减或等衰减组(n = 12)。高衰减组的微血管密度和巨噬细胞计数显着高于低衰减或等衰减组(P = 0.0372和P = 0.0476)。在30个高分化至中分化的肝癌中,中分化成分的微血管密度显着高于高分化成分的微血管密度(P <0.0001)。但是,中分化成分的巨噬细胞计数显着低于高分化成分(P <0.0001)。所有中分化成分在CTHA上均表现出明显的高度衰减。当局限于高度分化的肝癌时,肿瘤血管与肿瘤中的巨噬细胞计数相关。 TAM在其多步发展的早期阶段可能在促进HCC的血管生成中起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号