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Pokemon Silencing Leads to Bim-Mediated Anoikis of Human Hepatoma Cell QGY7703

机译:宠物小精灵沉默导致Bim介导的人类肝癌细胞QGY7703的失语症。

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摘要

Pokemon is an important proto-oncogene that plays a critical role in cellular oncogenic transformation and tumorigenesis. Anoikis, which is regulated by Bim-mediated apoptosis, is critical to cancer cell invasion and metastasis. We investigated the role of Pokemon in anoikis, and our results show that Pokemon renders liver cells resistant to anoikis via suppression of Bim transcription. We knocked-down Pokemon in human hepatoma cells QGY7703 with small interfering RNAs (siRNA). Knockdown of Pokemon alone did not significantly affect the growth and survival of QGY7703 cells but notably enhanced their sensitivity to apoptotic stress due to the presence of chemical agents or cell detachment, thereby inducing anoikis, as evidenced by flow cytometry and caspase-3 activity assays. In contrast, ectopic expression of Pokemon in HL7702 cells led to resistance to anoikis. Dual-luciferase reporter and ChIP assays illustrated that Pokemon suppressed Bim transcription via direct binding to its promoter. Our results suggest that Pokemon prevents anoikis through the suppression of Bim expression, which facilitates tumor cell invasion and metastasis. This Pokemon-Bim pathway may be an effective target for therapeutic intervention for cancer.
机译:宠物小精灵是重要的原癌基因,在细胞致癌转化和肿瘤发生中起关键作用。受Bim介导的细胞凋亡调节的Anoikis对癌细胞的侵袭和转移至关重要。我们调查了口袋妖怪在阳极中的作用,我们的结果表明,口袋妖怪通过抑制Bim转录使肝细胞对阳极具有抗性。我们用小干扰RNA(siRNA)敲低了人类肝癌细胞QGY7703中的神奇宝贝。通过流式细胞仪和caspase-3活性测定可以证明,单独敲除Pokemon不会显着影响QGY7703细胞的生长和存活,但由于存在化学试剂或细胞分离,可显着提高其对凋亡压力的敏感性,从而诱导失神经。相比之下,口袋妖怪在HL7702细胞中的异位表达导致了对阳极的抗性。双重荧光素酶报告基因和ChIP分析表明,Pokemon通过直接与其启动子结合而抑制了Bim转录。我们的研究结果表明,口袋妖怪通过抑制Bim表达来预防神经过敏,从而促进肿瘤细胞的侵袭和转移。该口袋妖怪-Bim途径可能是癌症治疗干预的有效靶点。

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