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作 者:曹颖[1] 金哲[2] 徐丁洁[1] 赵舒[1] 杜晨光[1] 董玉山[1]
机构地区:[1]河北联合大学中医学院,河北唐山063000 [2]北京中医药大学东方医院,北京100078
出 处:《时珍国医国药》2014年第8期1825-1827,共3页Lishizhen Medicine and Materia Medica Research
基 金:国家自然科学基金(No.30873278);河北联合大学博士科研启动项目(No.35755599)
摘 要:目的探讨中药清毒栓治疗宫颈高危型HPV感染的分子机制。方法以HPV18阳性的宫颈癌细胞系HeLa为细胞模型,清毒栓水提醇沉液、β-榄香烯、干扰素α-2b进行干预;分别采用Western blot及Real-time PCR检测MHC-Ⅰ抗原呈递通路相关内质网分子伴侣CNX、CRT、BIP的蛋白及基因表达差异。结果与对照组相比,3种药物均可不同程度的上调内质网分子伴侣CRT与CNX的蛋白表达,但对CRT与CNX的基因表达无影响(P>0.05);干扰素α-2b可上调BIP的蛋白表达(P<0.05),对BIP的基因表达无影响(P>0.05);清毒栓及β-榄香烯可上调BIP的基因表达,但对其蛋白表达无影响(P>0.05)。结论中药清毒栓及其有效成分之一β-榄香烯可通过上调内质网分子伴侣CNX及CRT的蛋白表达,促进宫颈癌细胞系HeLa的抗原呈递。Objective To explore the mechanism of Qingdu Suppository (QDS) in the treatment of high risk HPV infection. Methods Human cervical cancer cell line HeLa ( HPV 18 positive) was cutured in vitro and treated by the extract of QDS, β - elemene and IFNα - 2b. The protein and gene expression of MHC - I antigen presentation associated endoplasmic reticulum molecular chaperons including CNX, CRT and BIP were detected by Western blot and Real -time PCR independently. Result- s These three agents increased the protein expression of CNX and CRT in different degrees, whereas no significant difference was observed in gene expression of the two molecules( P〉0.05 ). IFNα- 2b up- regulated the protein expression of BIP( P〈0.05 ) but had no effect on its gene expression( P〉0.05 ). QDS and β-elemene increased the gene expression of BIP(P〈0.05 ) but had no effect on its protein expression(P〉0.05). Conclusion QDS and β-elemene as one of effective constituents in QDS both promote antigen presentation through up - regulating the protein expression of CNX and CRT function as molecular chaperones. This should be the key site in mechanism of action.
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