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肥大细胞促进非霍奇金淋巴瘤中的血管生成。一项基于与微血管密度关系的免疫组织化学研究。

Mast cells contribute to the angiogenesis in non-Hodgkin lymphoma. An immunohistochemical study based on the relationship with microvessel density.

作者信息

Duşe Adina Octavia, Ceauşu Raluca Amalia, Mezei T, Cîmpean Anca Maria, Gaje Puşa, Ioniţă Hortensia, Jung I

机构信息

Department of Histology, Victor Babeş University of Medicine and Pharmacy, Timisoara, Romania.

出版信息

Rom J Morphol Embryol. 2011;52(3 Suppl):1091-6.

Abstract

Only few data are available in the literature concerning angiogenesis in hematological malignancies. Non-Hodgkin lymphoma classified on the base of molecular profile is frequently characterized by unpredictable behavior that seems to be related to tumor cells and also to the tumor microenvironment. The tumor microenvironment contains blood vessels and a large variety of cells that can play an important role to the progression of angiogenesis and tumor growth. From these, mast cells have been shown to be a source of angiogenic factors. The aim of this work was to investigated the relationships between mast cells and blood vessels in non-Hodgkin lymphoma and reactive lymphoid tissue from three different anatomical sites. Using double immunostaining method CD34/mast cell tryptase we noticed that mast cell density was significantly lower in the follicular lymphoma than in diffuse type lymphoma. The morphology of vessels, the presence of pillars and splitting suggested that intussusceptions is the main mechanism of angiogenesis. In the cases with primary lymphoma of the spleen, we found few mast cells and a high number of blood vessels. Our data suggest that lymphoma-associated angiogenesis is driven in part by the tumor microenvironment, and particularly, by mast cells. On the other hand, our results support the organ-specific tumor-associated angiogenesis in malignant non-Hodgkin lymphoma.

摘要

关于血液系统恶性肿瘤中血管生成的文献资料很少。基于分子特征分类的非霍奇金淋巴瘤通常具有不可预测的行为,这似乎与肿瘤细胞以及肿瘤微环境有关。肿瘤微环境包含血管和多种细胞,这些细胞对血管生成和肿瘤生长的进展可能起着重要作用。其中,肥大细胞已被证明是血管生成因子的来源。这项工作的目的是研究非霍奇金淋巴瘤以及来自三个不同解剖部位的反应性淋巴组织中肥大细胞与血管之间的关系。使用双重免疫染色方法(CD34/肥大细胞类胰蛋白酶),我们注意到滤泡性淋巴瘤中的肥大细胞密度明显低于弥漫型淋巴瘤。血管的形态、柱的存在和分支表明套叠是血管生成的主要机制。在脾原发性淋巴瘤的病例中,我们发现肥大细胞数量少而血管数量多。我们的数据表明,淋巴瘤相关的血管生成部分是由肿瘤微环境驱动的,特别是由肥大细胞驱动。另一方面,我们的结果支持恶性非霍奇金淋巴瘤中器官特异性的肿瘤相关血管生成。

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