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潜伏膜蛋白1介导IL-2Rα上调促进NK/T细胞淋巴瘤的形成和化疗耐药 被引量:1
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作者 Liang Wang Xi-wen Bi +4 位作者 yu-jia zhu Ying-zhi He Qiu-yu Lai Zhong-jun Xia Qing-qing Cai 《癌症》 SCIE CAS CSCD 2019年第7期305-316,共12页
背景与目的 NK/T细胞淋巴瘤(natural killer/T-cell lymphoma,NKTCL)是一种高度侵袭性的非霍奇金淋巴瘤,经常发生化疗耐药。可溶性白细胞介素-2受体α(IL-2 receptorα,IL-2Rα)在NKTCL患者中血清水平升高,并与疗效和生存期显著相关。... 背景与目的 NK/T细胞淋巴瘤(natural killer/T-cell lymphoma,NKTCL)是一种高度侵袭性的非霍奇金淋巴瘤,经常发生化疗耐药。可溶性白细胞介素-2受体α(IL-2 receptorα,IL-2Rα)在NKTCL患者中血清水平升高,并与疗效和生存期显著相关。本研究旨在通过代表性细胞系中过表达IL-2Rα来探讨IL-2Rα的潜在作用。方法在人NK细胞系NK-92和NKTCL细胞系SNK-6中检测IL-2Rα的水平。使用慢病毒载体在NK-92细胞中表达潜伏膜蛋白1(latent membrane protein 1,LMP1),以及在NK-92和SNK-6细胞中表达IL-2Rα,分析这些基因在增殖、凋亡、细胞周期分布和化疗敏感性中的生物学功能。结果 IL-2Rα在SNK-6细胞中的表达水平显著高于NK-92细胞。在NK-92细胞中表达LMP1可以显著上调IL-2Rα水平,而MAPK/NF-κB途径相关蛋白的选择性抑制剂可以显著下调IL-2Rα。在SNK-6细胞中IL-2Rα的过表达通过改变细胞周期分布促进细胞增殖,并诱导产生对吉西他滨、多柔比星和门冬酰胺酶的耐药,这些效应可以被抗IL-2Rα抗体逆转。结论我们的研究显示,在NKTCL细胞中LMP1激活MAPK/NF-κB途径,从而上调IL-2Rα表达。IL-2Rα过表达促进NKTCL的生长和化疗耐药,表明该白细胞介素受体可作为潜在的治疗靶点。 展开更多
关键词 NK/T细胞淋巴瘤 潜伏膜蛋白1 Epstein–Barr病毒 白细胞介素-2受体α
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IL-2Rα up-regulation is mediated by latent membrane protein 1 and promotes lymphomagenesis and chemotherapy resistance in natural killer/T-cell lymphoma 被引量:4
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作者 Liang Wang Xi-wen Bi +4 位作者 yu-jia zhu Ying-zhi He Qiu-yu Lai Zhong-jun Xia Qing-qing Cai 《Cancer Communications》 SCIE 2018年第1期667-676,共10页
Background:Natural killer/T-cell lymphoma(NKTCL)is a highly aggressive non-Hodgkin lymphoma often resistant to chemotherapy.Serum level of soluble IL-2 receptorα(IL-2Rα)is elevated in NKTCL patients and correlates s... Background:Natural killer/T-cell lymphoma(NKTCL)is a highly aggressive non-Hodgkin lymphoma often resistant to chemotherapy.Serum level of soluble IL-2 receptorα(IL-2Rα)is elevated in NKTCL patients and correlates signifi-cantly with treatment response and survival.In the current study we examined the potential role of IL-2Rαby over-expressing IL-2Rαin representative cell lines.Methods:Levels of IL-2Rαwere evaluated in the human natural killer cell line NK-92 and the NKTCL cell line SNK-6.Lentiviral vectors were used to express latent membrane protein 1(LMP1)in NK-92 cells,and IL-2Rαin both NK-92 and SNK-6 cells.The biological effects of these genes on proliferation,apoptosis,cell cycle distribution,and chemosensitiv-ity were analyzed.Results:Expression of IL-2Rαwas significantly higher in SNK-6 cells than in NK-92 cells.Expressing LMP1 in NK-92 cells remarkably up-regulated IL-2Rαlevels,whereas selective inhibitorss of the proteins in the MAPK/NF-κB pathway significantly down-regulated IL-2Rα.IL-2Rαoverexpression in SNK-6 cells promoted cell proliferation by altering cell cycle distribution,and induced resistance to gemcitabine,doxorubicin,and asparaginase.These effects were reversed by an anti-IL-2Rαantibody.Conclusions:Our results suggest that LMP1 activates the MAPK/NF-κB pathway in NKTCL cells,up-regulating IL-2Rαexpression.IL-2Rαoverexpression promotes growth and chemoresistance in NKTCL,making this interleukin receptor a potential therapeutic target. 展开更多
关键词 Natural killer/T-cell lymphoma Latent membrane protein 1 Epstein-Barr virus Interleukin-2 receptor alpha
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