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Depletion of anti-CD47mAb in plasma by genetically modified cells for pre-transfusion testing
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作者 Fei Wang Wenting Wang +7 位作者 Xiaoshuang Wu Zhixin Liu Yafen Wang Rong Zhang Shunli Gu qunxing an Yaozhen Chen Xingbin Hu 《Genes & Diseases》 SCIE CSCD 2024年第5期102-104,共3页
Allogeneic red blood cell(RBC)transfusion is commonly performed in medical practice because of its efficacy and low-risk level.However,pre-transfusion tests are susceptible to monoclonal antibody(mAb)interference.1 Cu... Allogeneic red blood cell(RBC)transfusion is commonly performed in medical practice because of its efficacy and low-risk level.However,pre-transfusion tests are susceptible to monoclonal antibody(mAb)interference.1 Currently,mAb therapies are being developed to treat many diseases,such as cancer.However,certain mAbs,such as anti-CD38mAb and anti-CD47mAb,can bind to RBC membranes;this binding interferes with pre-transfusion tests.2 CD47 has gained considerable attention in recent years because of its potential as a therapeutic target for hematologic malignancies and solid tumors.3 The binding of anti-CD47mAb to RBCs may lead to false-positive results in pan-agglutination tests and cause delays and risks in establishing compatible RBCs for transfusion. 展开更多
关键词 CD47 TRANSFUSION DISEASES
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Apogossypolone对人前列腺癌LNCaP移植瘤的生长抑制作用(英文)
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作者 Yaozhen Chen Haishan Chen +6 位作者 Chen Chen Xiaofeng Huang Shijie Mu Mengyao Zhang Xingbin Hu qunxing an Xianqing Zhang 《The Chinese-German Journal of Clinical Oncology》 CAS 2012年第1期33-36,共4页
Objective:The aim of this study was to investigate the inhibitory effect of apogossypolone (ApoG2) on subcutaneous implants of human LNCaP prostatic carcinoma cells, and explore its mechanism. Methods:To establish hum... Objective:The aim of this study was to investigate the inhibitory effect of apogossypolone (ApoG2) on subcutaneous implants of human LNCaP prostatic carcinoma cells, and explore its mechanism. Methods:To establish human LNCaP prostatic carcinoma cell line subcutaneous xenograft models and observe the inhibitory effect of ApoG2 on the tumor model. Immunohistochemistry was employed to observe the expression of Bcl-2, PCNA, CD31, caspase-3 and-8 in tumor tissues. The microvessel density was calculated. Results:ApoG2 could obviously inhibit the growth of subcutaneous prostatic carcinoma implant. ApoG2 decreased the expression of PCNA and CD31, and increased the expression of caspases-3,-8 in tumor tissues. Conclusion:ApoG2 has an inhibitory effect on prostatic carcinoma implants. 展开更多
关键词 前列腺癌细胞 抑制作用 植入 人类 caspase-3 免疫组织化学方法 半胱天冬酶-3 上皮
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