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MiRNA-214 promotes the pyroptosis and inhibits the proliferation of cervical cancer cells via regulating the expression of NLRP3

机译:MiRNA-214促进糊酶通过调节NLRP3的表达来抑制宫颈癌细胞的增殖

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Inflammasome mediates the maturation of interleukin-1 beta (IL-1 beta) and IL-18, triggers the pyroptosis and associates with multiple autoimmune diseases. In light of this, we hope to investigate the regulatory role of miRNA-214 in the inflammasome of cervical cancer. With the samples collected from 50 cervical cancer patients and 50 age-matched healthy subjects, real-time PCR and Western blotting were employed to detect the mRNA and/or protein expression profiles of the NOD-like receptor protein family, including NLRP1, NLRP3, NLRC4, Caspase-1, IL-1 beta, IL-18 and miR-214. Corresponding plasmids were used to transfect the Hela, HCC94, Siha or HUCEI, normal cell lines to upregulate or downregulate the expression of targeted genes and to construct the cervical cancer models on rats. In addition, RT-PCR and Western blot were also considered to detect the expression of miR-214 and pyroptosis-related genes, while the pyroptosis of cells was evaluated by using the caspase-1 activity detection kit. Downregulation of miR-214 was found in the cervical cancer patients and the cervical cancer cell lines (** P <0.01), while overexpression of miR-214 could induce the pyroptosis of cervical cancer cell by targeting NLRP3. In cervical cancer patients, miR-214 and NLRP3 are downregulated, while upregulation of miR-214, by enhancing the expression of NLRP3, can advance the pyroptosis of cervical cancer cells. In addition, we, for the first time, clarify the correlation of cervical cancer with the miR-214 and NLRP3.
机译:炎症小体介导白细胞介素-1β(IL-1β)和IL-18的成熟,触发上睑下垂并与多种自身免疫疾病相关。有鉴于此,我们希望研究miRNA-214在宫颈癌炎症中的调节作用。从50名宫颈癌患者和50名年龄匹配的健康受试者中采集样本,采用实时PCR和Western blotting检测NOD样受体蛋白家族的mRNA和/或蛋白质表达谱,包括NLRP1、NLRP3、NLRC4、Caspase-1、IL-1β、IL-18和miR-214。用相应的质粒转染Hela、HCC94、Siha或HUCEI等正常细胞系,上调或下调靶基因的表达,构建大鼠宫颈癌模型。此外,RT-PCR和Western blot也被用于检测miR-214和热下垂相关基因的表达,同时使用caspase-1活性检测试剂盒评估细胞的热下垂。在宫颈癌患者和宫颈癌细胞系(**P<0.01)中发现miR-214的下调,而miR-214的过度表达可通过靶向NLRP3诱导宫颈癌细胞的热下垂。在宫颈癌患者中,miR-214和NLRP3表达下调,而miR-214的上调通过增强NLRP3的表达,可以促进宫颈癌细胞的热下垂。此外,我们首次阐明了宫颈癌与miR-214和NLRP3的相关性。

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