首页> 美国卫生研究院文献>Acta Histochemica et Cytochemica >Inhibitory Effects of Anti-VEGF Antibody on the Growth and Angiogenesis of Estrogen-induced Pituitary Prolactinoma in Fischer 344 Rats: Animal Model of VEGF-targeted Therapy for Human Endocrine Tumors
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Inhibitory Effects of Anti-VEGF Antibody on the Growth and Angiogenesis of Estrogen-induced Pituitary Prolactinoma in Fischer 344 Rats: Animal Model of VEGF-targeted Therapy for Human Endocrine Tumors

机译:抗VEGF抗体对Fischer 344大鼠雌激素诱导的垂体泌乳素瘤的生长和血管生成的抑制作用:针对人内分泌肿瘤的VEGF靶向治疗动物模型

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摘要

Estrogen-induced pituitary prolactin-producing tumors (PRLoma) in F344 rats express a high level of vascular endothelial growth factor (VEGF) associated with marked angiogenesis and angiectasis. To investigate whether tumor development in E2-induced PRLoma is inhibited by anti-VEGF monoclonal antibody (G6-31), we evaluated tumor growth and observed the vascular structures. With simultaneous treatment with G6-31 for the latter three weeks of the 13-week period of E2 stimulation (E2+G6-31 group), the following inhibitory effects on the PRLoma were observed in the E2+G6-31 group as compared with the E2-only group. In the E2+G6-31 group, a tendency to reduction in pituitary weight was observed and significant differences were observed as (1) reductions in the Ki-67-positive anterior cells, (2) increases in TUNEL-positive anterior cells, and (3) repair of the microvessel count by CD34-immunohistochemistry. The characteristic “blood lakes” in PRLomas were improved and replaced by repaired microvascular structures on 3D observation using confocal laser scanning microscope. These inhibitory effects due to anti-VEGF antibody might be related to the autocrine/paracrine action of VEGF on the tumor cells, because VEGF and its receptor are co-expressed on the tumor cells. Thus, our results demonstrate that anti-VEGF antibody exerted inhibitory effects on pituitary tumorigenesis in well-established E2 induced PRLomas.
机译:F344大鼠的雌激素诱导的垂体催乳激素产生肿瘤(PRLoma)表达高水平的血管内皮生长因子(VEGF),与明显的血管生成和血管扩张有关。为了研究E2诱导的PRLoma中的肿瘤发展是否受到抗VEGF单克隆抗体(G6-31)的抑制,我们评估了肿瘤的生长并观察了血管结构。在E2刺激的13周周期的后三周,同时用G6-31治疗(E2 + G6-31组),与E2 + G6-31组相比,对PRLoma有以下抑制作用仅E2组。在E2 + G6-31组中,观察到垂体重量减少的趋势,并且观察到了显着差异:(1)Ki-67阳性前细胞减少,(2)TUNEL阳性前细胞增加,以及(3)通过CD34-免疫组织化学修复微血管计数。使用共聚焦激光扫描显微镜进行3D观察后,PRLomas中特征性的“血湖”得到了改善并被修复的微血管结构所取代。由于抗VEGF抗体的这些抑制作用可能与VEGF对肿瘤细胞的自分泌/旁分泌作用有关,因为VEGF及其受体在肿瘤细胞上共表达。因此,我们的结果证明,抗VEGF抗体在成熟的E2诱导的PRLomas中对垂体肿瘤发生具有抑制作用。

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