Department of Pathology, University of Medicine and Pharmacy, 38 Ghe Marinescu Street, Targu Mures, 540139, Romania.
Recent Pat Anticancer Drug Discov. 2013 May;8(2):183-90.
The aim of our study was to correlate Maspin expression, a serine protease with possible antiangiogenic and antiproliferative effects, with angiogenesis and to realize a synthesis of the literature data regarding the novel patented compounds used in colorectal cancer (CRC).
In 110 cases with CRC, immunohistochemical stains were performed using Maspin, p53, VEGFA, CD31, and CD105. The results were correlated with the tumor stage and microsatellite status. A new scoring system for Maspin, based on the dual cytoplasmic-nuclear expression, with possible predictive value, was proposed.
The angiogenesis presented an oscillating pattern, the VEGF expression was more intense in Stage IV, but the endothelial area that quantified with both CD31 and CD105 was smaller than in those cases diagnosed in Stages II and III. Most of the p53 negative cases with Maspin nuclear predominance, which seems to respond to 5-Fluorouracil, were microsatellite instability (MSI) cases. In Stage II, Maspin nuclear positivity was more specific for pT4 tumors and aggressive cases with high p53 index. Thirty-three percent of CRC diagnosed in Stage II and 27% of those from Stage III presented Maspin expression in the endothelial cells. No cases from Stage IV had Maspin vascular positivity.
Maspin nuclear expression, associated with p53 ones, might be used either to select the high-risk microsatellite stable (MSS) colorectal carcinomas diagnosed in Stage II or those MSI cases which can respond to 5-Fluorouracil.
我们研究的目的是将丝氨酸蛋白酶 Maspin 的表达与血管生成相关联,并对用于结直肠癌 (CRC) 的新型专利化合物的文献数据进行综合分析。
在 110 例 CRC 病例中,使用 Maspin、p53、VEGFA、CD31 和 CD105 进行免疫组织化学染色。结果与肿瘤分期和微卫星状态相关联。提出了一种基于双细胞质-核表达的新型 Maspin 评分系统,具有潜在的预测价值。
血管生成呈波动模式,VEGF 表达在 IV 期更为强烈,但用 CD31 和 CD105 定量的内皮区域小于 II 期和 III 期诊断的病例。大多数 Maspin 核优势且 p53 阴性的病例似乎对 5-氟尿嘧啶有反应,这些病例都是微卫星不稳定 (MSI) 病例。在 II 期,Maspin 核阳性更特异于 pT4 肿瘤和具有高 p53 指数的侵袭性病例。在 II 期诊断的 CRC 中有 33%和 III 期的 27%病例的内皮细胞有 Maspin 表达。IV 期无病例的血管有 Maspin 阳性。
与 p53 相关的 Maspin 核表达,可能用于选择在 II 期诊断的高危微卫星稳定 (MSS) 结直肠癌,或那些对 5-氟尿嘧啶有反应的 MSI 病例。