摘要
目的:检测皮肤恶性黑色素瘤(CMM)组织中Runt相关转录因子3(Runx3)和Smad4蛋白的表达。方法:采用免疫组化SP法检测42例CMM、20例皮肤交界痣组织和20例正常皮肤组织中Runx3和Smad4蛋白的表达。结果:正常皮肤、皮肤交界痣及CMM组织中Runx3蛋白的阳性表达率分别为90.0%(18/20)、85.0%(17/20)和26.2%(11/42),3者相比,差异有统计学意义(χ2=31.371,P<0.001);正常皮肤、皮肤交界痣及CMM组织中Smad4蛋白的阳性表达率分别为85.0%(17/20)、85.0%(17/20)和42.9%(20/42),3者相比,差异有统计学意义(χ2=12.731,P=0.002)。CMM组织中Runx3和Smad4蛋白的表达存在关联性(rp=0.378,P=0.008)。结论:CMM组织中Runx3蛋白低表达或失表达,可能抑制了TGF-β/Smad4信号通路的激活,从而促进细胞的恶性转化和增殖。
Aim:To investigate the expressions of Runx3 and Smad4 protein in cutaneous malignant melanoma(CMM).Methods:The expressions of Runx3 and Smad4 protein were detected in 42 cases of CMM,20 cases of junctional nevus and 20 cases of normal skin specimens by SP immunohistochemical technique.Results: The positive expression rate of Runx3 protein in normal skin specimens, junctional nevus and CMM tissue was 90.0%(18/20),85.0%(17/20),and 26.2%(11/42),and there was significant difference(χ2=31.371,P0.001).The positive expression rate of Smad4 protein in normal skin specimens, junctional nevus and CMM tissue was 85.0%(17/20),85.0%(17/20), and 42.9%(20/42),and there was significant difference(χ2=12.731,P=0.002).The expression of Runx3 was positively associated with that of Smad4 in CMM tissue(rp=0.378,P=0.008).Conclusion:The low expression or deletion of Runx3 protein may effectively inhibit the over-activation of TGF-β/Smad4 signaling pathway, which might result in the malignant transformation and proliferation.
出处
《郑州大学学报(医学版)》
CAS
北大核心
2010年第6期980-983,共4页
Journal of Zhengzhou University(Medical Sciences)