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首页> 外文期刊>Pathology Research and Practice >Expression of protease-activated receptor-2 (PAR-2) in patients with nasopharyngeal carcinoma: correlation with clinicopathological features and prognosis.
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Expression of protease-activated receptor-2 (PAR-2) in patients with nasopharyngeal carcinoma: correlation with clinicopathological features and prognosis.

机译:蛋白酶激活受体2(PAR-2)在鼻咽癌患者中的表达:与临床病理特征和预后的关系。

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摘要

We aimed at determining whether the expression of protease-activated receptor 2 (PAR-2) is involved in the progression of nasopharyngeal carcinoma (NPC) and correlated with latent membrane protein 1 (LMP-1), matrix metalloproteinases-9 (MMP9), and angiogenesis of tumor. PAR-2, LMP-1, and MMP9 expressions were detected in 57 biopsies of primary NPC by immunohistochemistry. The presence of Epstein-Barr virus (EBV) was determined using EBER in situ hybridization, and intratumoral microvessels were highlighted by staining endothelial cells for anti-CD34. The correlations with immunostainings and clinicopathological factors, as well as the follow-up data of patients, were analyzed statistically. Strong expression of PAR-2 in 61.4% (35/57) of the biopsies was correlated with extensive lymph node metastasis and advanced stage of NPC. The patients with PAR-2/LMP-1 or PAR-2/MMP9 dual high-expression tumors had a significant worse prognosis than those with single protein high expression and dual low or negative expression tumors (P=0.013 and 0.004, respectively). Angiogenesis in the tumor is related to overall survival of NPC patients (P=0.001), and exhibits strong PAR-2 expression or LMP-1 expression in tumors associated with increased intratumoral microvessel density (P=0.026 and 0.006, respectively). PAR-2 is a possible mediator cooperating with LMP-1 and MMP9 to influence the progression of NPC by inducing angiogenesis and promoting lymph node metastasis.
机译:我们旨在确定蛋白酶激活受体2(PAR-2)的表达是否参与鼻咽癌(NPC)的发展并与潜伏膜蛋白1(LMP-1),基质金属蛋白酶9(MMP9)相关,和肿瘤的血管生成。通过免疫组织化学法在57例原发性NPC活检中检测到PAR-2,LMP-1和MMP9表达。使用EBER原位杂交确定爱泼斯坦-巴尔病毒(EBV)的存在,并通过对内皮细胞进行抗CD34染色来突出显示瘤内微血管。统计分析与免疫染色和临床病理因素的相关性,以及患者的随访数据。 PAR-2在61.4%(35/57)的活检组织中的强表达与广泛的淋巴结转移和NPC的晚期相关。 PAR-2 / LMP-1或PAR-2 / MMP9双重高表达肿瘤患者的预后显着低于单一蛋白高表达和双重低或阴性表达肿瘤的患者(分别为P = 0.013和0.004)。肿瘤中的血管生成与NPC患者的整体生存有关(P = 0.001),并且在与肿瘤内微血管密度增加相关的肿瘤中表现出强的PAR-2表达或LMP-1表达(分别为P = 0.026和0.006)。 PAR-2是可能与LMP-1和MMP9协同作用的介质,通过诱导血管生成和促进淋巴结转移来影响NPC的进程。

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