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作 者:于玢玢 朱雪琴[1] 池政兵[1] 汪俊[1] YU Bin-bin;ZHU Xue-qin;CHI Zheng-bing;WANG Jun(Department of Pediatric Dentistry,Shanghai Ninth People’s Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai 200011,China)
机构地区:[1]上海交通大学医学院附属第九人民医院儿童口腔科,上海交通大学口腔医学院,国家口腔医学中心,国家口腔疾病临床医学研究中心,上海市口腔医学重点实验室,上海市口腔医学研究所,200011
出 处:《北京口腔医学》2023年第3期159-162,共4页Beijing Journal of Stomatology
基 金:国家自然科学基金(82103074);上海市青年科技英才扬帆计划(21YF1424500)。
摘 要:目的 观察凝血因子2凝血酶受体(coagulation factor 2 thrombin receptor,F2R)抗体对小鼠口腔鳞癌细胞移植瘤生长抑制及对肿瘤、脾脏组织中髓源性抑制细胞(myeloid-derived suppressor cells,MDSCs)的影响。方法 通过皮下注射小鼠SCC-7细胞构建小鼠皮下移植瘤模型,实验组给予抗F2R抗体治疗,对照组注射与治疗组相同体积生理盐水。通过流式细胞仪分析移植瘤和脾脏组织中CD11b+Gr-1+MDSCs细胞比例。结果 抗F2R抗体治疗后,小鼠皮下移植瘤体积和重量明显降低,抑瘤率达66.7%(P<0.0001)。在小鼠皮下移植瘤抗F2R抗体组中,MDSCs细胞比例较对照组显著降低,分别为(0.876±0.259)%和(3.814±1.525)%(P<0.01)。而在小鼠脾脏组织抗F2R抗体组中,MDSCs细胞比例较对照组无显著差异。结论 抗F2R抗体治疗能抑制小鼠口腔鳞癌移植瘤模型肿瘤的进展,降低移植瘤组织中CD11b+Gr-1+MDSCs的比例。Objective To investigate the influence of coagulation factor 2 thrombin receptor(F2R)on the inhibition of tumor and the percentage of myeloid-derived suppressor cells(MDSCs)of tumor and spleen tissues in mice bearing oral squamous cell carcinoma.Methods The C3H xenograft model was set up through subcutaneously injecting mouse with oral squamous cell carcinomas cells SCC-7.The experimental group was treated with antibody F2R,and the control group was injected with normal saline.Flow cytometry was used to analyze the proportion of CD11b+Gr-1+MDSCs cells in the tumor and spleens of the C3H xenograft model.Results After therapy of antibody F2R,the tumor volume and weight in xenograft mice model were reduced significantly,and the tumor inhibition rate reached to 66.7%(P<0.0001).The flow cytometry showed that in the xenograft mice model,the proportion of MDSCs cells of antibody F2R group was significantly lower than that of the control group in tumor tissues(P<0.01).However,in the spleen tissues,there was no significant difference between the antibody F2R treatment group and the control group.Conclusions Antibody F2R treatment could inhibit the tumor progression in the xenograft model and reduce the proportion of CD11b+Gr-1+MDSCs cells in tumor tissues.
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