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PTPROt maintains T cell immunity in the microenvironment of hepatocellular carcinoma 被引量:2
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作者 Jiajie Hou Lei Deng +7 位作者 Han Zhuo Zhe Lin Yun Chen Runqiu Jiang Dianyu Chen Xudong Zhang Xingxu Huang Beicheng Sun 《Journal of Molecular Cell Biology》 SCIE CAS CSCD 2015年第4期338-350,共13页
Intratumoral T cells play a central role in anti-tumor immunity,and the balance between T effector cells(Teff)and regulatory T cells(Treg)affects the prognosis of cancer patients.However,educated by tumor microenviron... Intratumoral T cells play a central role in anti-tumor immunity,and the balance between T effector cells(Teff)and regulatory T cells(Treg)affects the prognosis of cancer patients.However,educated by tumor microenvironment,T cells frequently fail in their responsibility.In this study,we aimed to investigate the role of truncated isoform of protein tyrosine phosphatase receptor-typeO(PTPROt)in T cell-mediated anti-tumor immunity.We recruited 70 hepatocellular carcinoma(HCC)patients and 30 healthy volunteers for clinical investigation,and analyzed cellular tumor immunity by using ptpro^(-/-) C57BL/6 mice and NOD/SCID mice.PTPROt expression was significantly downregulated in human HCC-infiltrating T cells due to the hypoxia microenvironment;PTPROt expression highly correlated with the intratumoral Teff/Treg ratio and clinicopathologic characteristics.Moreover,PTPROt deficiency attenuated T cell-mediated anti-tumor immunity and remarkably promoted mouse HCC growth.Mechanistically,deletion of PTPROt decreased Teff quantity and quality through phosphorylation of lymphocyte-specific tyrosine kinase,but increased Treg differentiation through phosphorylation of signal transducer and activator of transcription 5.In support of the Teff/Treg homeostasis,PTPROt serves as an important tumor suppressor in HCC microenvironment. 展开更多
关键词 ptprot Teff TREG hepatocellular carcinoma
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硼替佐米联合阿糖胞苷诱导对K562细胞株PTPROt基因的影响 被引量:2
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作者 范丽霞 杨会彬 +4 位作者 化罗明 韩颖 薛华 季静 庞艳彬 《中国药业》 CAS 2014年第6期22-24,共3页
目的研究硼替佐米及阿糖胞苷序贯及联合用药对K562细胞的凋亡率的影响,同时观察硼替佐米是否经由PTPROt基因的表达上调促细胞凋亡。方法以慢性粒细胞白血病(CML)细胞的K562细胞为研究对象。不同用药组分别用药48 h,细胞选用噻唑蓝(MTT)... 目的研究硼替佐米及阿糖胞苷序贯及联合用药对K562细胞的凋亡率的影响,同时观察硼替佐米是否经由PTPROt基因的表达上调促细胞凋亡。方法以慢性粒细胞白血病(CML)细胞的K562细胞为研究对象。不同用药组分别用药48 h,细胞选用噻唑蓝(MTT)法检测细胞增殖抑制率,采用流式细胞术观察细胞抑制率与凋亡率情况,同时观察PTPROt基因表达情况。结果联合应用硼替佐米及阿糖胞苷组与分别应用硼替佐米及阿糖胞苷组两两相比差异有统计学意义(P<0.05)。联合用药使细胞凋亡率增加,序贯先应用阿糖胞苷后硼替佐米的细胞凋亡率最高,与单用硼替佐米及阿糖胞苷组两两相比差异有统计学意义(P<0.05)。应用硼替佐米后PTPROt基因表达明显上调。结论联合硼替佐米及阿糖胞苷,对白血病细胞株K562细胞有协同增强肿瘤细胞凋亡作用,其作用机制可能与上调PTPROt基因表达相关。 展开更多
关键词 硼替佐米 阿糖胞苷 K562细胞 ptprot基因 慢性粒细胞白血病
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