Takahashi H, Iizuka H, Katagiri M
Department of Dermatology, Asahikawa Medical College, Japan.
Arch Dermatol Res. 1990;282(1):8-11. doi: 10.1007/BF00505638.
The ras oncogene product, ras p21, is structurally homologous to guanine nucleotide-binding proteins, which play an important role in transmembrane signaling systems. Recently, enhanced expression of ras p21 has been reported in the psoriatic hyperproliferative epidermis, in which various alterations in the transmembrane signaling systems are well established. Since ras-proto-oncogenes are known to be activated by a single point mutation that is restricted to the amino acid residues either at position 12, 61 or in their vicinity, we investigated whether the increased expression of ras p21 in psoriatic epidermis is accompanied by mutation of the ras gene at these sites. The results obtained using samples from five cases of psoriasis revealed no evidence for such mutation. Although the psoriatic epidermis may exhibit enhanced expression of ras p21, this is apparently not accompanied by ras mutation.
原癌基因ras的产物ras p21在结构上与鸟嘌呤核苷酸结合蛋白同源,后者在跨膜信号系统中起重要作用。最近,有报道称ras p21在银屑病过度增殖的表皮中表达增强,而跨膜信号系统在该表皮中有多种改变。由于已知原癌基因ras可通过单个点突变激活,该突变仅限于第12位、61位氨基酸残基或其附近,我们研究了银屑病表皮中ras p21表达增加是否伴有这些位点的ras基因突变。对5例银屑病患者样本的检测结果未发现此类突变的证据。虽然银屑病表皮可能表现出ras p21表达增强,但显然这并不伴有ras突变。