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肝素酶在尤文肉瘤中的临床前和临床意义。

Pre-clinical and clinical significance of heparanase in Ewing's sarcoma.

机构信息

Cancer and Vascular Biology Research Center, The Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.

出版信息

J Cell Mol Med. 2011 Sep;15(9):1857-64. doi: 10.1111/j.1582-4934.2010.01190.x.

Abstract

Heparanase is an endoglycosidase that specifically cleaves heparan sulphate side chains of heparan sulphate proteoglycans, activity that is strongly implicated in cell migration and invasion associated with tumour metastasis, angiogenesis and inflammation. Heparanase up-regulation was documented in an increasing number of human carcinomas, correlating with reduced post-operative survival rate and enhanced tumour angiogenesis. Expression and significance of heparanase in human sarcomas has not been so far reported. Here, we applied the Ewing's sarcoma cell line TC71 and demonstrated a potent inhibition of cell invasion in vitro and tumour xenograft growth in vivo upon treatment with a specific inhibitor of heparanase enzymatic activity (compound SST0001, non-anticoagulant N-acetylated, glycol split heparin). Next, we examined heparanase expression and cellular localization by immunostaining of a cohort of 69 patients diagnosed with Ewing's sarcoma. Heparanase staining was noted in all patients. Notably, heparanase staining intensity correlated with increased tumour size (P = 0.04) and with patients' age (P = 0.03), two prognostic factors associated with a worse outcome. Our study indicates that heparanase expression is induced in Ewing's sarcoma and associates with poor prognosis. Moreover, it encourages the inclusion of heparanase inhibitors (i.e. SST0001) in newly developed therapeutic modalities directed against Ewing's sarcoma and likely other malignancies.

摘要

乙酰肝素酶是一种内切糖苷酶,可特异性切割乙酰肝素硫酸侧链的硫酸乙酰肝素蛋白聚糖,其活性强烈参与细胞迁移和侵袭,与肿瘤转移、血管生成和炎症有关。越来越多的人类癌中已证实乙酰肝素酶上调,与术后生存率降低和肿瘤血管生成增强相关。迄今为止,尚未有关于乙酰肝素酶在人类肉瘤中的表达和意义的报道。在这里,我们应用尤因氏肉瘤细胞系 TC71 并证实了一种特定的乙酰肝素酶酶活性抑制剂(化合物 SST0001,非抗凝 N-乙酰化,糖分裂肝素)在体外抑制细胞侵袭和体内肿瘤异种移植生长的强大作用。接下来,我们通过对 69 名诊断为尤因氏肉瘤的患者进行免疫染色检查了乙酰肝素酶的表达和细胞定位。在所有患者中均观察到乙酰肝素酶染色。值得注意的是,乙酰肝素酶染色强度与肿瘤大小增加(P=0.04)和患者年龄(P=0.03)相关,这两个预后因素与预后不良相关。我们的研究表明,乙酰肝素酶在尤因氏肉瘤中表达上调,并与不良预后相关。此外,它鼓励将乙酰肝素酶抑制剂(例如 SST0001)纳入针对尤因氏肉瘤和可能其他恶性肿瘤的新开发的治疗模式中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700c/3918042/db2be638cf00/jcmm0015-1857-f1.jpg

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