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Dickkopf-3 as a new potential marker for neoangiogenesis in colorectal cancer: Expression in cancer tissue and adjacent non-cancerous tissue1

机译:Dickkopf-3作为结直肠癌新血管生成的新潜在标志物:在癌组织和邻近的非癌组织中的表达1

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Gene expression of Dickkopf-3 (Dkk-3) has been shown to be upregulated in tumor endothelium of colorectal cancer (CRC). For the first time, we analyzed Dkk-3 protein expression in CRC and its potential as a marker for neoangiogenesis. We used tissue microarrays (TMAs) to investigate Dkk-3 in microvessels of 403 CRC samples, 318 appropriate adjacent non-cancerous samples and 127 normal colorectal samples. Of cancer samples with CD31-positive microvessels, 67.7% were positive for Dkk-3. Dkk-3 staining was demonstrated in endothelial cells of all microvessels in nearly all cases. Dkk-3-positive samples showed a higher mean microvessel count than did Dkk-3-negative samples (P = 0.001). Dkk-3 expression increased with rising numbers of microvessels per sample (P < 0.0001). In adjacent samples with CD31-positive microvessels, 56% were Dkk-3-positive in all microvessels. Similar to cancer samples, Dkk-3-positive adjacent samples had a higher mean microvessel count than did Dkk-3-negative samples (P < 0.0001), and Dkk-3 expression also increased with rising numbers of microvessels (P < 0.0001). All microvessels in normal mucosa samples were negative for Dkk-3.Dkk-3 can be considered a putative pro-angiogenic protein in neovascularization and may possibly be a marker for neoangiogenesis in CRC. Further investigations will elucidate whether Dkk-3 is a target structure for novel therapies.
机译:已显示Dickkopf-3(Dkk-3)的基因表达在大肠癌(CRC)的肿瘤内皮中被上调。首次,我们分析了Dkk-3蛋白在CRC中的表达及其作为新生血管生成标记的潜力。我们使用组织微阵列(TMA)研究了403个CRC样本,318个合适的相邻非癌性样本和127个正常结直肠样本的微血管中的Dkk-3。在带有CD31阳性微血管的癌症样本中,Dkk-3阳性的率为67.7%。在几乎所有情况下,在所有微血管的内皮细胞中均证实了Dkk-3染色。 Dkk-3阳性样本的平均微血管计数高于Dkk-3阴性样本(P = 0.001)。 Dkk-3表达随每个样品中微血管数量的增加而增加(P <0.0001)。在具有CD31阳性微血管的相邻样本中,所有微血管中56%的Dkk-3阳性。与癌症样本相似,Dkk-3阳性邻近样本的平均微血管计数高于Dkk-3阴性样本(P <0.0001),并且随着微血管数目的增加Dkk-3表达也增加(P <0.0001)。正常黏膜样品中的所有微血管均对Dkk-3阴性。Dkk-3在新血管形成中被认为是推定的促血管生成蛋白,可能是CRC中新血管生成的标志物。进一步的研究将阐明Dkk-3是否是新型疗法的靶标结构。

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