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膀胱癌中的肿瘤血管生成活性和血管存活能力。

Tumour angiogenic activity and vascular survival ability in bladder carcinoma.

作者信息

Papadopoulos I, Giatromanolaki A, Koukourakis M I, Sivridis E

机构信息

Department of Urology, Democritus University of Thrace, Alexandroupolis 68100, Greece.

出版信息

J Clin Pathol. 2004 Mar;57(3):250-5. doi: 10.1136/jcp.2003.012005.

Abstract

BACKGROUND

Tumour angiogenic activity (TAA) is an important prognostic factor in many human tumours, including transitional cell carcinomas of the urinary bladder. The new tumour vessels are formed in the invading tumour front. This peripheral tumour area is internalised as soon as the growing tumour forms a new front.

AIMS

To investigate and compare TAA with the ability of the tumour vasculature to survive (VSA) in inner tumour areas.

METHODS

Fifty one cystectomy specimens with transitional cell carcinoma of the urinary bladder were studied. Sections were stained immunohistochemically for endothelial cells and proliferation activity, using the monoclonal antibodies CD31 and MIB-1, respectively. TAA was studied at the invading tumour edge-designated as the mean number of blood vessels in three "hot spots" at this site. VSA was assessed by comparing the vascular density in peripheral and inner tumour areas.

RESULTS

High TAA at the invading tumour edge significantly correlated with lymph node involvement, but not with patient survival. Extensive lymphocytic infiltration was more frequent in tumours with high TAA. VSA was significantly higher in tumours of high proliferation index, high histological grade, advanced T stage, and poor prognosis. However, there was no association with metastasis to regional lymph nodes.

CONCLUSION

VSA and TAA provide a more complete profile of the tumour vasculature and are associated with aggressive tumour behaviour in transitional cell carcinomas of the urinary bladder. The qualitative information provided by VSA may be important for the identification of angiogenic tumours with differential responses to various antiangiogenic treatments.

摘要

背景

肿瘤血管生成活性(TAA)是许多人类肿瘤(包括膀胱移行细胞癌)的一个重要预后因素。新的肿瘤血管在侵袭性肿瘤前沿形成。一旦生长中的肿瘤形成新的前沿,这个周边肿瘤区域就会被内化。

目的

研究并比较TAA与肿瘤内部区域肿瘤血管生存能力(VSA)。

方法

对51例膀胱移行细胞癌膀胱切除术标本进行研究。分别使用单克隆抗体CD31和MIB-1对切片进行免疫组织化学染色,以检测内皮细胞和增殖活性。在侵袭性肿瘤边缘研究TAA,将其定义为该部位三个“热点”处血管的平均数量。通过比较周边和肿瘤内部区域的血管密度来评估VSA。

结果

侵袭性肿瘤边缘的高TAA与淋巴结受累显著相关,但与患者生存率无关。高TAA的肿瘤中广泛的淋巴细胞浸润更为常见。高增殖指数、高组织学分级、晚期T分期和预后不良的肿瘤中VSA显著更高。然而,与区域淋巴结转移无关。

结论

VSA和TAA能更全面地反映肿瘤血管系统,且与膀胱移行细胞癌的侵袭性肿瘤行为相关。VSA提供的定性信息对于识别对各种抗血管生成治疗有不同反应的血管生成性肿瘤可能很重要。

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