Kim Anthony W, Xu Xiulong, Hollinger Edward F, Gattuso Paolo, Godellas Constantine V, Prinz Richard A
Department of General Surgery, Rush Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
J Gastrointest Surg. 2002 Mar-Apr;6(2):167-72. doi: 10.1016/s1091-255x(01)00087-7.
Extracellular matrix degradation is an essential step that allows tumor cells to penetrate a tissue barrier and become metastatic. Heparanase-1 (HPR1) is an endoglycosidase that specifically degrades heparan sulfate proteoglycans, a chief component of the extracellular matrix. HPR1 is not expressed in normal epithelial cells but can be detected in a variety of malignancies. In the present study, we examined HPR1 expression in pancreatic cancer by using in situ hybridization and tested whether HPR1 expression correlated with any clinicopathlogic parameters. HPR1 was not detected in the ductal cells of normal pancreas samples obtained from 10 patients at autopsy. However, HPR1 was detected in 77 (78%) of 99 pancreatic adenocarcinomas. Among them, 69 (78%) of 89 primary pancreatic adenocarcinomas and 8 (80%) of the 10 metastases were HPR1 positive. Age, sex, tumor stage, and lymph node status were not predictive of HPR1 expression. Log-rank test of the Kaplan-Meier survival curves revealed that HPR1 expression in early-stage tumors was associated with decreased survival. HPR1 expression was frequent in pancreatic adenocarcinomas and was associated with decreased survival in early-stage tumors. This suggests that HPR1 may contribute to the highly invasive and early metastatic behavior of pancreatic cancer.
细胞外基质降解是肿瘤细胞穿透组织屏障并发生转移的关键步骤。乙酰肝素酶-1(HPR1)是一种内切糖苷酶,可特异性降解细胞外基质的主要成分硫酸乙酰肝素蛋白聚糖。HPR1在正常上皮细胞中不表达,但在多种恶性肿瘤中均可检测到。在本研究中,我们采用原位杂交技术检测胰腺癌中HPR1的表达,并测试HPR1表达是否与任何临床病理参数相关。在10例尸检获得的正常胰腺样本的导管细胞中未检测到HPR1。然而,在99例胰腺腺癌中有77例(78%)检测到HPR1。其中,89例原发性胰腺腺癌中有69例(78%),10例转移瘤中有8例(80%)HPR1呈阳性。年龄、性别、肿瘤分期和淋巴结状态均不能预测HPR1的表达。对Kaplan-Meier生存曲线进行对数秩检验显示,早期肿瘤中HPR1的表达与生存率降低相关。HPR1在胰腺腺癌中表达频繁,且与早期肿瘤的生存率降低相关。这表明HPR1可能促成了胰腺癌的高度侵袭性和早期转移行为。