Chen Qi, Lu Hong-sheng, Gan Mei-fu, Chen Lan-xi, He Kai, Fan Guang-min, Cao Xue-quan
Department of Clinical Laboratory, Taizhou Central Hospital, Taizhou, China E-mail :
Asian Pac J Cancer Prev. 2015;16(6):2495-9. doi: 10.7314/apjcp.2015.16.6.2495.
Mitogen-activated protein kinase/extracellular signal-regulated kinase kinase kinase 3 (MEKK3) is an important serine/threonine protein kinase and a member of the MAPK family. MEKK3 can effectively activate the MEK/ERK signaling pathway and promote an autocrine growth loop critical for tumor genesis, cell proliferation, terminal differentiation, apoptosis and survival. To explore the relationship between MEKK3 and cell apoptosis, clinicopathology and prognosis, we characterize the expression of MEKK3, pERK and FoxP3 in the renal clear cell carcinoma (RCCC). Protein expression was detected by tissue microarray and immunochemistry in 46 cases of RCCC and 28 control cases. Expression levels of CD3+ ,CD3+CD4+,CD3+CD8+,CD4+CD25+, CD4+CD25+ FoxP3+ were assessed by flow cytometry and analyzed for their association with pathological factors, correlation and prognosis in RCCC. Expression of MEKK3, pERK and FoxP3 was significantly up-regulated in RCCC as compared to control levels (p<0.01), associated with pathological grade (p<0.05)and clinical stage (p<0.05). CD4+CD25+ Foxp3+ Treg cells were also significantly increased in RCCC patients (p<0.05). Cox multivariate regression analysis showed that MEKK3, pERK expression and patholigical stage were independent prognostic factors in patients with RCCC (p<0.05). MEKK3 can be used as an important marker of early diagnosis and prognostic evaluation in RCCC. It may be associated with imbalance of anti-tumor immunity and overexpression of pERK. Expression of MEKK3 and pERK are significantly increased in RCCC, with protein expression and clinical stage acting as independent prognostic factors.
丝裂原活化蛋白激酶/细胞外信号调节激酶激酶激酶3(MEKK3)是一种重要的丝氨酸/苏氨酸蛋白激酶,属于丝裂原活化蛋白激酶(MAPK)家族。MEKK3能有效激活MEK/ERK信号通路,并促进对肿瘤发生、细胞增殖、终末分化、凋亡及存活至关重要的自分泌生长环。为探究MEKK3与细胞凋亡、临床病理及预后之间的关系,我们对肾透明细胞癌(RCCC)中MEKK3、pERK和FoxP3的表达进行了表征。采用组织芯片和免疫化学方法检测了46例RCCC病例和28例对照病例的蛋白表达情况。通过流式细胞术评估CD3+、CD3+CD4+、CD3+CD8+、CD4+CD25+、CD4+CD25+FoxP3+的表达水平,并分析其与RCCC病理因素、相关性及预后的关系。与对照水平相比,RCCC中MEKK3、pERK和FoxP3的表达显著上调(p<0.01),与病理分级(p<0.05)和临床分期(p<0.05)相关。RCCC患者中CD4+CD25+Foxp3+调节性T细胞也显著增加(p<0.05)。Cox多因素回归分析显示,MEKK3、pERK表达及病理分期是RCCC患者的独立预后因素(p<0.05)。MEKK3可作为RCCC早期诊断和预后评估的重要标志物。它可能与抗肿瘤免疫失衡及pERK过表达有关。RCCC中MEKKI和pERK的表达显著增加,蛋白表达和临床分期为独立预后因素。