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Different significance between intratumoral and peritumoral lymphatic vessel density in gastric cancer: a retrospective study of 123 cases

机译:胃癌肿瘤内和肿瘤周围淋巴管密度的不同意义:123例回顾性研究

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Background Patients with gastric cancer in China have worse outcome and poorer prognosis. Tumor-induced lymphangiogenesis plays a crucial role in metastasis and tumor progression. The intratumoral and peritumoral lymphatics were supposed to have different biological effects. Three major growth factors, vascular endothelial growth factor- (VEGF)-A, VEGF-C and VEGF-D, are involved in the activation process via their receptors (VEGFRs). The purpose of current study is to investigate the significant difference between intratumoral and peritumoral lymphatic vessel density (LVD) in gastric cancer and their correlations with lymphangiogenetic growth factors. Methods Intratumoral LVD (I-LVD) and peritumoral LVD (P-LVD) of 123 patients with primary gastric cancer were assessed after staining with D2-40, and confirmed by double staining with D2-40/CD34. Proliferative activity of lymphatics endothelium was evaluated by double staining with D2-40/Ki-67. The associations were analyzed between I-LVD/P-LVD and the expression level of VEGF-A, VEGF-C, VEGF-D and the receptor VEGFR-3, which was measured by immunohistochemistry (IHC). The correlations of I-LVD and P-LVD with patient prognosis were also valued. Results (1) The peritumoral lymphatics (PTLs) were relatively enlarged with dilated lumen compared with the intratumoral lymphatics (ITLs). Increased P-LVD was significantly higher than I-LVD ( P 0.05). (3) Proliferative activity of lymphatics endothelium was observed in PTLs, in spite of ITLs. (4) Increased P-LVD, but not I-LVD, was indicated to be an independent risk factor for lymph node metastasis by multivariate logistic regression analysis, and was related to worse disease-free survival and overall survival. Conclusions PTLs play roles in gastric cancer progression. Increased P-LVD, but not I-LVD, was significantly associated with VEGF-C/-D/VEGFR-3 system, and could be an independent risk factor for lymph node metastasis and a prognostic factor in gastric cancer.
机译:背景中国的胃癌患者预后较差,预后较差。肿瘤诱导的淋巴管生成在转移和肿瘤进展中起关键作用。肿瘤内和肿瘤周围淋巴管被认为具有不同的生物学效应。三种主要的生长因子,血管内皮生长因子-(VEGF)-A,VEGF-C和VEGF-D,通过其受体(VEGFR)参与激活过程。本研究的目的是研究胃癌的肿瘤内和肿瘤周围淋巴管密度(LVD)之间的显着差异及其与淋巴管生成生长因子的相关性。方法对123例原发性胃癌患者的瘤内LVD(I-LVD)和瘤周LVD(P-LVD)进行D2-40染色后评价,并经D2-40 / CD34双重染色证实。通过D2-40 / Ki-67双重染色评估淋巴管内皮细胞的增殖活性。分析了I-LVD / P-LVD与VEGF-A,VEGF-C,VEGF-D和受体VEGFR-3的表达水平之间的相关性,这是通过免疫组织化学(IHC)测定的。 I-LVD和P-LVD与患者预后的相关性也得到重视。结果(1)与瘤内淋巴管(ITL)相比,瘤腔周围淋巴管(PTL)相对增大,管腔扩张。 P-LVD增加明显高于I-LVD(P 0.05)。 (3)尽管有ITL,但在PTL中观察到了淋巴管内皮的增殖活性。 (4)多因素logistic回归分析表明,P-LVD升高而不是I-LVD是淋巴结转移的独立危险因素,并且与无病生存期和总生存期较差有关。结论PTLs在胃癌的进展中起作用。 P-LVD升高但I-LVD升高与VEGF-C / -D / VEGFR-3系统显着相关,并且可能是胃癌淋巴结转移的独立危险因素和预后因素。

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