Miettinen Markku, Lasota Jerzy
Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
Appl Immunohistochem Mol Morphol. 2005 Sep;13(3):205-20. doi: 10.1097/01.pai.0000173054.83414.22.
CD117 (KIT) is a type III receptor tyrosine kinase operating in cell signal transduction in several cell types. Normally KIT is activated (phosphorylated) by binding of its ligand, the stem cell factor. This leads to a phosphorylation cascade ultimately activating various transcription factors in different cell types. Such activation regulates apoptosis, cell differentiation, proliferation, chemotaxis, and cell adhesion. KIT-dependent cell types include mast cells, some hematopoietic stem cells, germ cells, melanocytes, and Cajal cells of the gastrointestinal tract, and neoplasms of these cells are examples of KIT-positive tumors. Other KIT-positive normal cells include epithelial cells in skin adnexa, breast, and subsets of cerebellar neurons. KIT positivity has been variably reported in sarcomas such as angiosarcoma, Ewing sarcoma, synovial sarcoma, leiomyosarcoma, and MFH; results of the last three are controversial. The variations in published data may result from incomplete specificity of some polyclonal antibodies, possibly contributed by too high dilutions. Also, KIT is expressed in pulmonary and other small cell carcinomas, adenoid cystic carcinoma, renal chromophobe carcinoma, thymic, and some ovarian and few breast carcinomas. A good KIT antibody reacts with known KIT positive cells, and smooth muscle cells and fibroblasts are negative. KIT deficiency due to hereditary nonsense/missense mutations leads to disruption of KIT-dependent functions such as erythropoiesis, skin pigmentation, fertility, and gastrointestinal motility. Conversely, pathologic activation of KIT through gain-of-function mutations leads to neoplasia of KIT-dependent and KIT-positive cell types at least in three different systems: mast cells/myeloid cells--mastocytosis/acute myeloid leukemia, germ cells--seminoma, and Cajal cells--gastrointestinal stromal tumors (GISTs). KIT tyrosine kinase inhibitors such as imatinib mesylate are the generally accepted treatment of metastatic GISTs, and their availability has prompted an active search for other treatment targets among KIT-positive tumors such as myeloid leukemias and small cell carcinoma of the lung, with variable and often nonconvincing results.
CD117(KIT)是一种III型受体酪氨酸激酶,在多种细胞类型的细胞信号转导中发挥作用。正常情况下,KIT通过与其配体干细胞因子结合而被激活(磷酸化)。这会引发磷酸化级联反应,最终激活不同细胞类型中的各种转录因子。这种激活调节细胞凋亡、细胞分化、增殖、趋化性和细胞黏附。依赖KIT的细胞类型包括肥大细胞、一些造血干细胞、生殖细胞、黑素细胞以及胃肠道的Cajal细胞,这些细胞发生的肿瘤就是KIT阳性肿瘤的例子。其他KIT阳性正常细胞包括皮肤附属器、乳腺中的上皮细胞以及小脑神经元亚群。在诸如血管肉瘤、尤因肉瘤、滑膜肉瘤、平滑肌肉瘤和恶性纤维组织细胞瘤等肉瘤中,KIT阳性率的报道各不相同;后三种肉瘤的结果存在争议。已发表数据的差异可能源于一些多克隆抗体的特异性不完全,这可能是由于稀释度过高所致。此外,KIT在肺和其他小细胞癌、腺样囊性癌、肾嫌色细胞癌、胸腺癌以及一些卵巢癌和少数乳腺癌中也有表达。一种良好的KIT抗体能与已知的KIT阳性细胞发生反应,而平滑肌细胞和成纤维细胞则为阴性。由于遗传性无义/错义突变导致的KIT缺陷会破坏依赖KIT的功能,如红细胞生成、皮肤色素沉着、生育能力和胃肠蠕动。相反,通过功能获得性突变导致的KIT病理性激活至少在三个不同系统中会引发依赖KIT和KIT阳性细胞类型的肿瘤形成:肥大细胞/髓细胞——肥大细胞增多症/急性髓细胞白血病、生殖细胞——精原细胞瘤、Cajal细胞——胃肠道间质瘤(GIST)。KIT酪氨酸激酶抑制剂如甲磺酸伊马替尼是转移性GIST的普遍接受的治疗方法,它们的出现促使人们积极在KIT阳性肿瘤如髓系白血病和肺小细胞癌中寻找其他治疗靶点,但结果各不相同且往往缺乏说服力。