Tojo M, Mori T, Kiyosawa H, Honma Y, Tanno Y, Kanazawa K Y, Yokoya S, Kaneko F, Wanaka A
Department of Cell Science, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima City, Japan.
Pathol Int. 1999 Aug;49(8):687-94. doi: 10.1046/j.1440-1827.1999.00938.x.
In basal cell nevus syndrome (BCNS) patients, mutations of a gene, patched (ptc), which encodes a putative signal transducer of sonic hedgehog protein (SHH), were found and are thought to be one of the major causes of BCNS. The SHH signaling pathway is an important developmental pathway, and ptc protein (PTC) is a suppressive component serving as a receptor for the secreted SHH. Another transmembrane protein, smoothened (SMO), forms a complex with PTC and regulates this signaling pathway. Recent transgenic studies have strengthened the importance of the SHH signaling system in the etiology of basal cell carcinoma (BCC). In this study, we examined the expression patterns of mRNA for ptc and smo in two different BCC subtypes and normal skin. We found that the expressions of ptc and smo mRNA were enhanced in the tumor nests of the nodular BCC, especially at the advancing portions, but were under the detectable level in the superficial BCC cases examined, indicating that ptc and smo mRNA expressions might be associated with BCC tumor progression and divide the BCC histologic types into two subtypes, superficial and nodular types. In addition, no obvious signals for ptc and smo mRNA were detected in the normal human epidermis, appendages, or seborrheic keratosis, indicating that the abnormal proliferation of follicular epithelial cells caused by ptc, smo and/or other genetic changes, which also cause ptc and smo overexpressions, might result in BCC tumor formation.
在基底细胞痣综合征(BCNS)患者中,发现了一种名为patched(ptc)的基因突变,该基因编码一种假定的音猬因子蛋白(SHH)信号转导分子,被认为是BCNS的主要病因之一。SHH信号通路是一条重要的发育通路,ptc蛋白(PTC)是一种抑制性成分,作为分泌型SHH的受体。另一种跨膜蛋白smoothened(SMO)与PTC形成复合物并调节该信号通路。最近的转基因研究强化了SHH信号系统在基底细胞癌(BCC)病因学中的重要性。在本研究中,我们检测了ptc和smo的mRNA在两种不同BCC亚型及正常皮肤中的表达模式。我们发现,ptc和smo mRNA的表达在结节型BCC的肿瘤巢中增强,尤其是在进展部位,但在所检测的浅表型BCC病例中低于可检测水平,这表明ptc和smo mRNA的表达可能与BCC肿瘤进展相关,并可将BCC组织学类型分为浅表型和结节型两种亚型。此外,在正常人类表皮、附属器或脂溢性角化病中未检测到ptc和smo mRNA的明显信号,这表明由ptc、smo和/或其他基因变化导致的毛囊上皮细胞异常增殖,同时也导致ptc和smo过表达,可能会导致BCC肿瘤形成。