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[乳腺癌发生发展过程中血管生成的评估]

[Evaluation of angiogenesis in the tumorigenesis and progression of breast cancer].

作者信息

Li Ying-jia, Deng Yong-jian, Wen Ge, Zhang Xue-lin

机构信息

Department of Ultrasound Diagnosis, Nanfang Hospital, Nanfang Medical University, Guangzhou 510515, China.

出版信息

Zhonghua Wai Ke Za Zhi. 2009 Apr 1;47(7):519-22.

Abstract

OBJECTIVES

To investigate the expression of CD34, vascular endothelial growth factor (VEGF) and its receptor Flk-1/KDR in precancerous lesion, atypical hyperplasia (AH) and infiltrating carcinoma of breast cancer and to explore the correlation between angiogenesis abnormality and the tumor progression.

METHODS

One hundred and sixty cases of resected tissues from breast cancer patients were enrolled in the study and were divided into 5 groups: 30 cases as normal controls, 30 cases with simple hyperplasia, 30 cases with AH, 20 cases with intraductal carcinoma in situ and 50 cases with infiltrating ductal carcinoma. The expression of CD34, VEGF and its receptor, Flk-1/KDR in those tissues were determined with immunohistochemical techniques. The micro vascular density (MVD) in those tissues was determined with the expression of CD34.

RESULTS

The expression level of CD34, VEGF and Flk-1/KDR were different among the groups, with the highest expression in the infiltrating ductal carcinoma group. With the progression of breast cancer, the major indexes showed no significant changes in the early stage of progression, but the expression of VEGF and Flk-1/KDR increased significantly from AH stage. Meanwhile, the MVD increased in the same way. There was significant difference between AH and intraductal carcinoma group in the expression of VEGF and Flk-1/KDR (P<0.05), but not in the MVD (P>0.05).

CONCLUSIONS

Abnormality in angiogenesis may be an early event in the tumorigenesis of breast cancer. Abnormal expression of VEGF and Flk-1/KDR may be the initiating factor of angiogenesis in the process of breast hyperplasia-AH-breast cancer, it could be the molecular target of early diagnosis and treatment.

摘要

目的

研究CD34、血管内皮生长因子(VEGF)及其受体Flk-1/KDR在乳腺癌癌前病变、非典型增生(AH)及浸润性癌中的表达情况,探讨血管生成异常与肿瘤进展之间的相关性。

方法

选取160例乳腺癌患者的手术切除组织,分为5组:正常对照组30例,单纯增生组30例,AH组30例,导管原位癌组20例,浸润性导管癌组50例。采用免疫组化技术检测这些组织中CD34、VEGF及其受体Flk-1/KDR的表达。通过CD34的表达情况测定这些组织中的微血管密度(MVD)。

结果

各组中CD34、VEGF及Flk-1/KDR的表达水平不同,浸润性导管癌组表达最高。随着乳腺癌的进展,主要指标在进展早期无明显变化,但从AH期开始VEGF及Flk-1/KDR的表达显著增加。同时,MVD也以相同方式增加。AH组与导管原位癌组在VEGF及Flk-1/KDR的表达上有显著差异(P<0.05),但在MVD方面无显著差异(P>0.05)。

结论

血管生成异常可能是乳腺癌发生的早期事件。VEGF及Flk-1/KDR的异常表达可能是乳腺增生-AH-乳腺癌过程中血管生成的起始因素,可能成为早期诊断和治疗的分子靶点。

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