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恶性和良性前列腺基质组织中神经纤毛蛋白-1的差异表达。

Differential expression of neuropilin-1 in malignant and benign prostatic stromal tissue.

作者信息

Vanveldhuizen Peter J, Zulfiqar Muhammad, Banerjee Snigdha, Cherian Rachel, Saxena Neela K, Rabe Amy, Thrasher J Brantley, Banerjee Sushanta K

机构信息

Cancer Research Unit, V.A. Medical Center, Research Division, Kansas City, MO 64128, USA.

出版信息

Oncol Rep. 2003 Sep-Oct;10(5):1067-71.

Abstract

Neuropilin-1 (NRP-1), a co-receptor for VEGF165, is overexpressed in various prostate cancer cell lines and in advanced prostate tumors. However, distribution of the NRP-1 in prostate tumors has not yet been evaluated. Using immunohistochemical analysis, we evaluated 21 archival prostate tumors and 5 benign glands for the expression of NRP-1. In addition, we utilized a quantitative RT-PCR method to examine mRNA expression in 9 additional prostate tumors obtained from radical prostatectomy specimens and compared this expression to the adjacent normal tissue. The RT-PCR analyses demonstrated overexpression of NRP-1 mRNA in malignant tissue samples by 10.0-fold as compared to adjacent normal tissue. By immunohistochemistry, NRP-1 protein was undetected or minimally detected in the epithelial tumor cells. However, NRP-1 immuno-reaction was detected in the surrounding tumor stroma. Variable immuno-reaction for NRP-1 was also seen in the adjacent normal tumor stroma and the stroma of the benign prostate samples. These observations suggest that neuropilin-1 is expressed in the prostatic stromal cells, not epithelial tumor cells, and this expression is significantly increased in the malignant phenotype.

摘要

神经纤毛蛋白-1(NRP-1)是血管内皮生长因子165(VEGF165)的共受体,在多种前列腺癌细胞系及晚期前列腺肿瘤中过表达。然而,NRP-1在前列腺肿瘤中的分布情况尚未得到评估。我们采用免疫组织化学分析方法,评估了21例存档前列腺肿瘤及5例良性腺体中NRP-1的表达情况。此外,我们运用定量逆转录聚合酶链反应(RT-PCR)方法检测了另外9例取自根治性前列腺切除术标本的前列腺肿瘤中的mRNA表达,并将该表达与相邻正常组织进行比较。RT-PCR分析显示,与相邻正常组织相比,恶性组织样本中NRP-1 mRNA的表达高出10.0倍。通过免疫组织化学方法,在肿瘤上皮细胞中未检测到或仅微量检测到NRP-1蛋白。然而,在肿瘤周围基质中检测到了NRP-1免疫反应。在相邻正常肿瘤基质及良性前列腺样本的基质中也观察到了NRP-1的不同免疫反应。这些观察结果表明,神经纤毛蛋白-1在前列腺基质细胞而非肿瘤上皮细胞中表达,且这种表达在恶性表型中显著增加。

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