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干细胞因子(SCF)的免疫组织化学定位及其受体原癌基因产物c-Kit(c-KIT)在黑素细胞肿瘤中的比较

Immunohistochemical localisation of stem cell factor (SCF) with comparison of its receptor c-Kit proto-oncogene product (c-KIT) in melanocytic tumours.

作者信息

Takahashi H, Saitoh K, Kishi H, Parsons P G

机构信息

Division of Dermatology, Sapporo-Kosei General Hospital, Japan.

出版信息

Virchows Arch. 1995;427(3):283-8. doi: 10.1007/BF00203396.

Abstract

In order to characterise the distribution and role of stem cell factor (SCF), a recently-reported growth factor for normal melanocytes, we carried out an immunohistochemical study on benign and malignant melanocytic tumours with a comparison with the presence of its receptor c-Kit proto-oncogene product (c-KIT). In normal skin, SCF was mainly observed in endothelial cells of blood vessels but not frequently in basal melanocytes, whereas c-KIT was predominantly localised in tissue mast cells. In benign neoplastic melanocytes (common melanocytic naevi), localisation of SCF and c-KIT was complementary: SCF was mostly found in dermal naevus cells while c-KIT was revealed in epidermal naevus cells, although the expression of the latter antigen was not frequent. Malignant melanoma cells showed less frequent expression of these antigens than those in benign lesions. Of five cultured melanoma cell lines, SCF was observed in only one, and c-KIT was not found in any melanoma cells. No quantitative or qualitative alterations assessed by Western blot analysis were induced in the presence of phenotypic modifiers (sodium butyrate and HMBA). Present data suggest that loss of SCF expression in neoplastic melanocytes is commonly associated with malignant transformation of pigment cells rather than loss of its receptor c-KIT.

摘要

为了描述干细胞因子(SCF)的分布和作用,SCF是一种最近报道的对正常黑素细胞起作用的生长因子,我们对良性和恶性黑素细胞肿瘤进行了免疫组织化学研究,并与它的受体c-Kit原癌基因产物(c-KIT)的存在情况进行了比较。在正常皮肤中,SCF主要在血管内皮细胞中观察到,而在基底黑素细胞中不常见,而c-KIT主要定位于组织肥大细胞中。在良性肿瘤性黑素细胞(普通黑素细胞痣)中,SCF和c-KIT的定位是互补的:SCF大多在真皮痣细胞中发现,而c-KIT在表皮痣细胞中显示,尽管后一种抗原的表达并不常见。恶性黑色素瘤细胞与良性病变中的细胞相比,这些抗原的表达频率较低。在五个培养的黑色素瘤细胞系中,仅在一个细胞系中观察到SCF,在任何黑色素瘤细胞中均未发现c-KIT。在存在表型修饰剂(丁酸钠和六亚甲基双乙酰胺)的情况下,通过蛋白质印迹分析评估未诱导出定量或定性改变。目前的数据表明,肿瘤性黑素细胞中SCF表达的丧失通常与色素细胞的恶性转化有关,而不是与其受体c-KIT的丧失有关。

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