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血管生成因子中期因子在神经纤维瘤病1型(NF1)缺陷的施万细胞中异常表达,并且是神经纤维瘤来源细胞的促分裂原。

The angiogenic factor midkine is aberrantly expressed in NF1-deficient Schwann cells and is a mitogen for neurofibroma-derived cells.

作者信息

Mashour G A, Ratner N, Khan G A, Wang H L, Martuza R L, Kurtz A

机构信息

Vincent T Lombardi Cancer Center, Department of Neurosurgery, Georgetown University School of Medicine, 3970 Reservoir Road NW, Washington DC 20007, USA.

出版信息

Oncogene. 2001 Jan 4;20(1):97-105. doi: 10.1038/sj.onc.1204026.

Abstract

Loss of the tumor suppressor gene NF1 in neurofibromatosis type 1 (NF1) contributes to the development of a variety of tumors, including malignant peripheral nerve sheath tumors (MPNST) and benign neurofibromas. Of the different cell types found in neurofibromas, Schwann cells usually provide between 40 and 80%, and are thought to be critical for tumor growth. Here we describe the identification of growth factors that are upregulated in NF1-/- mouse Schwann cells and are potential regulators of angiogenesis and cell growth. Basic fibroblast growth factor (FGF-2), platelet-derived growth factor (PDGF) and midkine (MK) were found to be induced by loss of neurofibromin and MK was further characterized. MK was induced in human neurofibromas, schwannomas, and various nervous system tumors associated with NF1 or NF2; midkine showed an expression pattern overlapping but distinct from its homolog pleiotrophin (PTN). Immunohistochemistry revealed expression of MK in S-100 positive Schwann cells of dermal and plexiform neurofibromas, and in endothelial cells of tumor blood vessels, but not in normal blood vessels. Furthermore, MK demonstrated potent mitogenic activity for human systemic and brain endothelial cells in vitro and stimulated proliferation and soft agar colony formation of human MPNST derived S100 positive cells and fibroblastoid cells derived from an NF1 neurofibroma. The data support a possible central role for MK as a mediator of angiogenesis and neurofibroma growth in NF1. Oncogene (2001) 20, 97 - 105.

摘要

1型神经纤维瘤病(NF1)中肿瘤抑制基因NF1的缺失会促使包括恶性外周神经鞘瘤(MPNST)和良性神经纤维瘤在内的多种肿瘤发生。在神经纤维瘤中发现的不同细胞类型中,施万细胞通常占40%至80%,并且被认为对肿瘤生长至关重要。在此,我们描述了在NF1基因敲除小鼠施万细胞中上调且可能是血管生成和细胞生长调节因子的生长因子的鉴定。发现碱性成纤维细胞生长因子(FGF-2)、血小板衍生生长因子(PDGF)和中期因子(MK)是由神经纤维瘤蛋白缺失诱导产生的,并对MK进行了进一步的特性分析。MK在人类神经纤维瘤、神经鞘瘤以及与NF1或NF2相关的各种神经系统肿瘤中被诱导产生;中期因子显示出一种与其同源物多效生长因子(PTN)重叠但不同的表达模式。免疫组织化学显示,MK在皮肤和丛状神经纤维瘤的S-100阳性施万细胞以及肿瘤血管的内皮细胞中表达,但在正常血管中不表达。此外,MK在体外对人全身和脑内皮细胞表现出强大的促有丝分裂活性,并刺激源自人MPNST的S100阳性细胞和源自NF1神经纤维瘤的成纤维样细胞的增殖和软琼脂集落形成。这些数据支持MK作为NF1中血管生成和神经纤维瘤生长的介质可能发挥核心作用。《癌基因》(2001年)第20卷,第97 - 105页

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