1.Diagnostic value of fibrinogen for the cause of pleural effusion
Chinese Journal of Primary Medicine and Pharmacy 2011;18(15):2061-2062
ObjectiveTo investigate the level of fibrinogen in pleural effusion in tuberculous and malignant pleural effusion in content and nature of the diagnostic value of pleural effusion. MethodsCoagulation in STAGOcompact automated analyzer was determined to detect 42 cases of tuberculous pleural effusion and 38 cases of malignant pleural effusion levels of fibrinogen in patients with pleural effusion. ResultsThe level of fibrinopen in Tuberculous pleural effusion in malignant group was lover than that of tubeeculous group. Fibrinogen concentration of pleural effusion groups was significantly different( P < 0.05). Thickenig in tuberculous group was greater than that in malignant pleural group(P < 0.05). ConclusionThe determination of fibrinogen in pleural effusion had a considerable diagnostic value in differentiating tuberculosis from malignant pleural effusion.
2.circ_0001821 regulates the proliferation, apoptosis, migration and invasion of cutaneous squamous cell carcinoma A431 cells by targeting miR-203
XIAO Chuanliu ; LIN Hongchang ; LUO Yang ; CUI Lixia
Chinese Journal of Cancer Biotherapy 2021;28(9):893-899
[摘 要] 目的: 探讨circ_0001821通过靶向miR-203调控皮肤鳞状细胞癌(cutaneous squamous cell carcinoma,CSCC)A431细胞增殖、凋亡、迁移及侵袭的分子机制。方法:选取2018年2月至2019年8月海南医学院第二附属医院收治的39例CSCC患者的癌及配对癌旁组织,以及人CSCC细胞系A431,用qPCR法检测CSCC癌和癌旁组织中circ_0001821的表达水平。利用脂质体转染技术,分别将si-circ_0001821、si-NC、miR-203 mimic、miR-NC、si-circ_0001821与anti-miR-NC、si-circ_0001821与anti-miR-203转染至A431细胞,用qPCR法检测转染细胞中circ_0001821和miR-203的表达水平,MTT法、流式细胞术和Transwell实验分别检测A431细胞的增殖、凋亡、迁移及侵袭能力,WB法检测细胞中增殖、凋亡、迁移及侵袭相关蛋白的表达水平。通过Circinteractome数据库预测circ_0001821与miR-203存在结合位点,双荧光素酶报告基因实验验证circ_0001821与miR-203的靶向关系。结果:CSCC组织中circ_0001821的表达水平显著高于癌旁组织(P<0.01)。转染si-circ_0001821可显著降低细胞中circ_0001821的表达水平(P<0.01),降低细胞增殖、迁移和侵袭能力(均P<0.01),提高细胞凋亡率(P<0.01)。双荧光素酶报告基因实验证实,circ_0001821可靶向结合miR-203。转染miR-203 mimic可显著降低A431细胞的增殖、迁移和侵袭能力(均P<0.01),提高细胞凋亡率(P<0.01)。共转染si-circ_0001821与anti-miR-203可明显逆转下调circ_0001821表达对A431细胞增殖、迁移、侵袭及凋亡的调控作用。结论:circ_0001821通过靶向miR-203调控CSCC细胞A431的增殖、迁移、侵袭能力及细胞凋亡。