Mazurek A, Kuc P, Terlikowski S, Laudanski T
Department of Pathophysiology of Pregnancy, Medical University of Bialystok, 15-276 Bialystok, Poland.
Neoplasma. 2006;53(3):242-6.
The formation of new blood vessels in endometrial cancer tissue is a main process, which leads to tumor progression, and is connected with tumor expansion and invasiveness. The aim of the study was evaluation of thymidine phosphorylase protein (TP) expression in human endometrial cancer cells by immunohistochemistry and comparison obtained data with intensity of angiogenesis process and clinicopathological factors as FIGO stage of disease and histopathologic grade. Endometrial cancer specimens were obtained from 55 postmenopausal patients (aged 52 to 74 years) underwent total abdominal hysterectomy with bilateral salpingo-oophorectomy. None of patients received preoperative pelvic irradiation. Histopathological typing and grading of the endometrial tumors (G-1, G-2, G-3) as well as myometrial invasion (<1/2, >1/2) were assessed using standard criteria, on hematoxylin-eosin sections. At the surgery, FIGO clinical stage of disease was determined. Thymidine phosphorylase overexpression was observed in 23 of 55 (41.8%) cases of endometrial cancer. Although we found no statistically significant differences in TP expression between histopathologic grades, particular FIGO stages showed a significant trend of increase TP tumor overexpression. Thymidine phosphorylase overexpression cases demonstrate higher intensity of angiogenesis in comparison to negative samples and results are statistically significant for t-test (p<0.0001). The most intensive new blood vessel formation was observed in G-2 of tumor differentiation grade (p=0.013 for ANOVA test) Mean angiogenic points density (APD) values in cases of G-1 histopathologic grade reached 135.7; values of G-2 and G-3 grades reached 213.8 and 162.8, respectively. Mean intensity of angiogenesis in the first FIGO stage of disease reached 160.0 APD, in stage II 205.6 APD, and in the third 286.9, respectively. Angiogenesis was more intensive in cases of advanced tumors - analysis of variance (ANOVA) confirmed statistically significant differences in APD values between FIGO stage groups (p=0.0007). In conclusion, thymidine phosphorylase expression correlates with increased microvessel density in endometrial cancer. The intensity of angiogenesis process increases according to FIGO stage of disease, which is connected with progressing of cancer disease. Thymidine phosphorylase can play an important role in endometrial cancer progression and could offer additional information about advance of disease.
子宫内膜癌组织中新生血管的形成是一个主要过程,它导致肿瘤进展,并与肿瘤的扩展和侵袭性相关。本研究的目的是通过免疫组织化学评估人子宫内膜癌细胞中胸苷磷酸化酶蛋白(TP)的表达,并将所得数据与血管生成过程的强度以及临床病理因素(如疾病的FIGO分期和组织病理学分级)进行比较。从55例接受全腹子宫切除术及双侧输卵管卵巢切除术的绝经后患者(年龄52至74岁)中获取子宫内膜癌标本。所有患者均未接受术前盆腔放疗。使用苏木精-伊红切片,根据标准标准评估子宫内膜肿瘤的组织病理学类型和分级(G-1、G-2、G-3)以及肌层浸润情况(<1/2、>1/2)。在手术时确定疾病的FIGO临床分期。在55例子宫内膜癌病例中,有23例(41.8%)观察到胸苷磷酸化酶过表达。尽管我们发现组织病理学分级之间TP表达无统计学显著差异,但特定的FIGO分期显示出TP肿瘤过表达有显著增加趋势。与阴性样本相比,胸苷磷酸化酶过表达病例显示出更高的血管生成强度,t检验结果具有统计学意义(p<0.0001)。在肿瘤分化程度为G-2时观察到最强烈的新生血管形成(方差分析p=0.013)。组织病理学分级为G-1的病例中平均血管生成点密度(APD)值达到135.7;G-2和G-3分级的值分别达到213.8和162.8。疾病的FIGO第一期平均血管生成强度达到160.0 APD,第二期为205.6 APD,第三期为286.9 APD。晚期肿瘤病例中的血管生成更强烈——方差分析(ANOVA)证实FIGO分期组之间的APD值存在统计学显著差异(p=0.0007)。总之,胸苷磷酸化酶表达与子宫内膜癌中微血管密度增加相关。血管生成过程的强度根据疾病的FIGO分期增加,这与癌症疾病的进展相关。胸苷磷酸化酶可能在子宫内膜癌进展中起重要作用,并可为疾病进展提供额外信息。