Inamine M, Nagai Y, Hirakawa M, Mekaru K, Yagi C, Masamoto H, Aoki Y
Department of Obstetrics and Gynecology, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan.
J Obstet Gynaecol. 2008 Aug;28(6):634-7. doi: 10.1080/01443610802323542.
The human enzyme heparanase has been shown to function in tumour progression, metastatic spread and tumour angiogenesis. The aim of the present study was to assess heparanase expression assessed by immunohistochemical staining (IHC) in endometrial cancer in correlation with clinicopathological factors. A total of 52 endometrial cancers were obtained from previously untreated patients (median age, 56 years, range, 35-80 years). The expression of heparanase was evaluated by using IHC with anti-heparanase polyclonal antibody. This antibody was raised by immunising a rabbit with a peptide containing the amino acid residues from 238 to 250 of the heparanase. The IHC data were used to determine the relationship between heparanase expression, and clinicopathological parameters. IHC showed that the heparanase was expressed in 23 of 52 (44.2%) endometrial cancers. Heparanase was abundantly and equally expressed in both the cytoplasm and the cell membrane of the cells in endometrial cancer. Strong heparanase-positive staining was also seen at the invasive front of the tumour into myometrium. The expression was significantly related to lymph-vascular space involvement (p = 0.0028), depth of myometrial invasion (p = 0.0026), and histological tumour grade (p = 0.0135). In six tumours with positive lymph nodes, the heparanase expression was observed as being higher compared with tumours with negative lymph nodes, which was not significant (p = 0.2349). In terms of peritoneal cytology, ovarian metastasis, and cervical invasion, we observed no significant difference in the heparanase expression assessed by IHC. These results suggest that the expression of heparanase may promote tumour invasion into myometrium and lymph vascular space in endometrial cancer.
人源酶类乙酰肝素酶已被证明在肿瘤进展、转移扩散和肿瘤血管生成中发挥作用。本研究旨在评估通过免疫组织化学染色(IHC)检测的乙酰肝素酶在子宫内膜癌中的表达,并将其与临床病理因素相关联。总共从先前未经治疗的患者中获取了52例子宫内膜癌样本(中位年龄56岁,范围35 - 80岁)。使用抗乙酰肝素酶多克隆抗体通过IHC评估乙酰肝素酶的表达。该抗体是通过用包含乙酰肝素酶第238至250位氨基酸残基的肽免疫兔子制备而成。IHC数据用于确定乙酰肝素酶表达与临床病理参数之间的关系。IHC显示,52例子宫内膜癌中有23例(44.2%)表达乙酰肝素酶。在子宫内膜癌细胞的细胞质和细胞膜中,乙酰肝素酶均大量且均匀表达。在肿瘤侵入肌层的浸润前沿也可见强烈的乙酰肝素酶阳性染色。该表达与淋巴血管间隙受累(p = 0.0028)、肌层浸润深度(p = 0.0026)和组织学肿瘤分级(p = 0.0135)显著相关。在6例淋巴结阳性的肿瘤中,观察到乙酰肝素酶表达高于淋巴结阴性的肿瘤,但差异无统计学意义(p = 0.2349)。在腹膜细胞学、卵巢转移和宫颈浸润方面,我们观察到通过IHC评估的乙酰肝素酶表达无显著差异。这些结果表明,乙酰肝素酶的表达可能促进子宫内膜癌向肌层和淋巴血管间隙的侵袭。