%0 Journal Article %T Toll样受体4在淋巴瘤细胞株中的表达及其对细胞增殖和耐药的影响 %A 克晓燕 %A 张巍 %A 王晶 %A 闫新星 %J 肿瘤防治研究 %D 2016 %R 10.3971/j.issn.1000-8578.2016.06.001 %X 摘要 目的 探讨Toll样受体4(Toll-like receptor 4,TLR4)在人淋巴瘤细胞株中的表达及其对细胞增殖和耐药的影响。方法 采用RT-PCR、qPCR和Western blot检测8株淋巴瘤细胞株中TLR4 mRNA及蛋白的表达情况并筛选出TLR4高表达株,对高表达株进行基因测序以排除MyD88 L265P基因突变。将TLR4高标达细胞株分为空白对照组、TAK-242组、细菌脂多糖(lipopolysaccharides, LPS)组和LPS+TAK-242组,分别进行细胞增殖和阿霉素耐药实验。采用CCK-8试剂盒检测其增殖活性和细胞杀伤率,用Western blot法检测增殖细胞核抗原(proliferating cell nuclear antigen, PCNA)和P-糖蛋白(P-glycoprotein, P-gp)的变化。结果 8株淋巴瘤细胞株中TLR4 mRNA和蛋白广泛表达,其中Burkitt淋巴瘤细胞株Raji的表达水平最高。Raji细胞MyD88基因为野生型。与空白对照组相比,TAK-242和LPS+TAK-242组Raji细胞的增殖活性无明显改变(P=2.19, P=1.85),LPS组Raji细胞的增殖活性明显升高(P=0.016), LPS组PCNA蛋白表达明显升高(P=0.009)。阿霉素在半数抑制浓度下各组杀伤率分别为:空白对照组(49.23±2.03)%、TAK-242组(51.41±1.12)%、LPS组(24.65±3.17)%、LPS+TAK-242组(41.17±2.69)%,可见LPS组细胞杀伤率明显降低(P=0.002)。P-gp蛋白表达明显升高(P=0.001)。结论 TLR4分子在淋巴瘤细胞株中广泛表达,尤以Burkitt淋巴瘤细胞株Raji最高,激活TLR4可以促使肿瘤细胞增殖和耐药,其机制可能与PCNA和P-gp的表达上调有关 %K A Case Report %K Effect of Cisplatin Combined with Buzhong Yiqi Decoction on survivin Expression in Transplantation Tumor of Nude Mice with A549/DDP Cells %K Current Research Status of NF-kappa B Related Molecular Pathway in Diffuse Large B Cell Lymphoma %K Effects of FEN1 Overexpression on Biological Behaviors of Hepatocellular Carcinoma Cells and Prognosis of Patients %K UGCG is Involved in Oxaliplatin Resistance Mechanism of Human Colon Cancer Through Regulating MDR1/P-gp Expression %K Predictive Factors for Customizing Chemotherapy on Advanced Lung Adenocarcinoma %K Bioinformatics Analysis of Genes Related to Multidrug Resistance in Ovarian Cancer %K Knockdown of PKD1 Decreased Sensitivity of Human Salivary Gland Adenoid Cystic Carcinoma Cell Line ACC2 to Paclitaxel %K Impact of miRNA-200c on Methotrexate Resistance of Non-small Cell Lung Cancer Cells A549 %K Clinical Characteristics and Prognosis of 123 Patients with Diffuse Large B-cell Lymphoma of Waldeyer’s Ring %K Mechanism of Jinlong Capsule Reversing Paclitaxel Resistance of A549 Cells Investigated by System Biology Technology %K miR-143/145 Cluster Regulate Multi-drug Resistance of Small Cell Lung Cancer %U http://www.zlfzyj.com/CN/abstract/abstract8763.shtml