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VEGF-A和血管生成素在软骨肿瘤中的差异表达及白细胞介素-1β的调控作用

Differential expression of VEGF-A and angiopoietins in cartilage tumors and regulation by interleukin-1beta.

作者信息

Kalinski Thomas, Krueger Sabine, Sel Saadettin, Werner Kerstin, Ropke Martin, Roessner Albert

机构信息

Department of Pathology, Otto-von-Guericke-University, Magdeburg, Germany.

出版信息

Cancer. 2006 May 1;106(9):2028-38. doi: 10.1002/cncr.21848.

Abstract

BACKGROUND

Vascular endothelial growth factor (VEGF)-A and angiopoietin (Ang)-1 and Ang-2 are key factors in angiogenic signaling. In this study the expression of these factors was identified in cartilage tumors. As interleukin (IL)-1beta has been found to be an indispensable factor in angiogenic signaling, we further analyzed the effect of IL-1beta on the expression of VEGF-A, Ang-1, and Ang-2 using a previously established cell culture model.

METHODS

Surgical specimens of enchondromas, conventional chondrosarcomas, and dedifferentiated chondrosarcomas were obtained from 72 patients. VEGF-A, Ang-1, and Ang-2 mRNA expression was detected by conventional and quantitative reverse transcription polymerase chain reaction (PCR). VEGF-A expression was also detected by immunohistochemistry or Western blot.

RESULTS

Differential expression of VEGF-A, Ang-1, and Ang-2 was clearly demonstrated in cartilage tumors. VEGF-A expression was positively correlated with the tumor type. Higher VEGF-A expression levels were detected in conventional chondrosarcomas Grades II and III (using a 3-tier grading system) than in dedifferentiated chondrosarcomas (P < .05). A typical pattern of VEGF-A isoforms was identified, including VEGF(121), VEGF(145), VEGF(165), and VEGF(189). Ang-1 presented as a low-level transcript with slightly elevated levels in chondrosarcomas (P < .05). Highly variable Ang-2 expression levels were detected in solitary cases of conventional chondrosarcomas. IL-1beta regulated VEGF-A and Ang-1 expressions in a dose-dependent manner. Whereas low IL-1beta concentrations increased VEGF-A and Ang-1 transcription, high IL-1beta concentrations had the opposite effect. IL-1beta did not activate Ang-2 expression.

CONCLUSIONS

Angiogenic signaling in cartilage tumors is variable and at least partly regulable by IL-1beta. The findings are of therapeutic relevance, either as a desired effect or a side effect in medical treatment.

摘要

背景

血管内皮生长因子(VEGF)-A、血管生成素(Ang)-1和Ang-2是血管生成信号传导中的关键因子。在本研究中,这些因子在软骨肿瘤中的表达得以确定。由于白细胞介素(IL)-1β已被发现是血管生成信号传导中不可或缺的因子,我们使用先前建立的细胞培养模型进一步分析了IL-1β对VEGF-A、Ang-1和Ang-2表达的影响。

方法

从72例患者获取内生软骨瘤、传统型软骨肉瘤和去分化型软骨肉瘤的手术标本。通过常规和定量逆转录聚合酶链反应(PCR)检测VEGF-A、Ang-1和Ang-2 mRNA表达。VEGF-A表达也通过免疫组织化学或蛋白质印迹法检测。

结果

在软骨肿瘤中明确显示了VEGF-A、Ang-1和Ang-2的差异表达。VEGF-A表达与肿瘤类型呈正相关。在传统型软骨肉瘤II级和III级(采用三级分级系统)中检测到的VEGF-A表达水平高于去分化型软骨肉瘤(P <.05)。确定了VEGF-A异构体的典型模式,包括VEGF(121)、VEGF(145)、VEGF(165)和VEGF(189)。Ang-1表现为低水平转录本,在软骨肉瘤中水平略有升高(P <.05)。在传统型软骨肉瘤的个别病例中检测到高度可变的Ang-2表达水平。IL-1β以剂量依赖性方式调节VEGF-A和Ang-1表达。低浓度IL-1β增加VEGF-A和Ang-1转录,而高浓度IL-1β则产生相反作用。IL-1β未激活Ang-2表达。

结论

软骨肿瘤中的血管生成信号传导是可变的,且至少部分可由IL-1β调节。这些发现具有治疗相关性,无论是作为医疗中的预期效果还是副作用。

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