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血管内皮生长因子/血管通透因子在小鼠腹水肿瘤中的显著表达。

Significant expression of vascular endothelial growth factor/vascular permeability factor in mouse ascites tumors.

作者信息

Luo J C, Yamaguchi S, Shinkai A, Shitara K, Shibuya M

机构信息

Department of Genetics, Institute of Medical Science, University of Tokyo, Japan.

出版信息

Cancer Res. 1998 Jun 15;58(12):2652-60.

PMID:9635593
Abstract

Vascular endothelial growth factor (VEGF), also known as vascular permeability factor, is believed to be a potent mediator of peritoneal fluid accumulation and angiogenesis and of tumor growth in ascites tumor. Such roles, however, have not been generally established because of insufficient quantitative and systemic analyses. To address this, we examined the expression of VEGF in 13 mouse ascites tumors (5 sarcomas, 3 carcinomas, 2 lymphomas, 1 leukemia, 1 mastocytoma, and 1 plasmacytoma). Using a newly developed sensitive and specific radioreceptor binding assay and functional assays, we found that active VEGF was significantly accumulated (6-850 ng/ml) in the ascites fluids of all 13 tumors. VEGF concentrations are higher in the tumors of sarcoma and carcinoma origin (430.4 +/- 234.2 ng/ml) than in those of lymphoma and hematological tumor origin (19.2 +/- 10.45 ng/ml). VEGF that accumulated in the peritoneal fluids or expressed in the ascites tumor cells was easily visualized with immunoprecipitation Western blot analysis with a rough correlation to the expression levels of VEGF gene in these tumor cells, suggesting that the tumor cells, at least in part, contributed to the production of the VEGF that accumulated in the ascites fluid. Most ascites tumors expressed VEGF; the 164-amino acid isoform was predominant, the 120-amino acid isoform was less abundant, and the 188-amino acid isoform was least abundant. Several representative ascites tumors expressed similar, if not higher, levels of VEGF when they were cultured at normoxic states, suggesting that they expressed VEGF at high levels in a constitutive manner. The microvessel densities in the peritoneal walls of tumor-bearing mice, which are significantly higher than those in normal mice, basically correlated to but did not parallel the VEGF concentrations in their respective ascites fluids. Thus, a complicated relationship may exist between the VEGF production and angiogenesis associated with ascites tumor in vivo. Taken together, our observations suggest that VEGF plays a fundamental role in ascites tumor formation; however, its importance may vary according to tumor origin.

摘要

血管内皮生长因子(VEGF),也被称为血管通透因子,被认为是腹水肿瘤中腹腔积液、血管生成以及肿瘤生长的强效介质。然而,由于缺乏充分的定量和系统分析,这些作用尚未得到普遍证实。为了解决这一问题,我们检测了13种小鼠腹水肿瘤(5种肉瘤、3种癌、2种淋巴瘤、1种白血病、1种肥大细胞瘤和1种浆细胞瘤)中VEGF的表达。使用新开发的灵敏且特异的放射受体结合测定法和功能测定法,我们发现活性VEGF在所有13种肿瘤的腹水中均有显著蓄积(6 - 850 ng/ml)。肉瘤和癌起源的肿瘤中VEGF浓度(430.4 +/- 234.2 ng/ml)高于淋巴瘤和血液肿瘤起源的肿瘤(19.2 +/- 10.45 ng/ml)。通过免疫沉淀Western印迹分析,很容易观察到蓄积在腹腔积液中或在腹水肿瘤细胞中表达的VEGF,且其与这些肿瘤细胞中VEGF基因的表达水平大致相关,这表明肿瘤细胞至少部分促成了蓄积在腹水液中的VEGF的产生。大多数腹水肿瘤表达VEGF;其中以164个氨基酸的异构体为主,120个氨基酸的异构体含量较少,188个氨基酸的异构体含量最少。几种具有代表性的腹水肿瘤在常氧状态下培养时表达的VEGF水平相似,甚至更高,表明它们以组成性方式高水平表达VEGF。荷瘤小鼠腹膜壁中的微血管密度显著高于正常小鼠,其与各自腹水液中的VEGF浓度基本相关,但并不平行。因此,体内腹水肿瘤的VEGF产生与血管生成之间可能存在复杂的关系。综上所述,我们的观察结果表明VEGF在腹水肿瘤形成中起重要作用;然而,其重要性可能因肿瘤起源而异。

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