MIS18BP1通过失活P53信号通路促进膀胱癌细胞的增殖和生长。

IF 2.8 4区 医学 Q2 ONCOLOGY
WenJing Cao, XueYing Tan, Xuze Li, YuLin Wang, YuQing Zhai, ZongLiang Zhang, JiangShui Yuan, WeiQing Song
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引用次数: 0

摘要

MIS18结合蛋白1 (MIS18BP1)是MIS18复合体的一个亚基,特异积累于晚期g1着丝粒,调控癌细胞的凋亡、增殖和迁移。MIS18BP1调控膀胱癌(BCa)细胞发育的机制此前并不为人所知。我们利用癌症基因组图谱(TCGA)、基因表达图谱(GEO)和通用蛋白数据库分析MIS18BP1在BCa中的差异表达。采用qRT-PCR检测MIS18BP1 mRNA的表达。western blot和免疫组化(IHC)染色检测MIS18BP1蛋白的表达。用LV -MIS18BP1 -RNAi载体转染T24细胞,降低MIS18BP1的表达。我们通过一系列的实验来检测T24的存活、增殖和迁移。流式细胞术检测细胞凋亡。western blot检测P53、BAX和Cleaved Casepase-3的表达。分析P53抑制剂治疗前后P53凋亡相关蛋白、细胞增殖和迁移情况。MIS18BP1在BCa组织中的表达高于对照组。其表达与临床分期、浸润深度及淋巴结转移有关。我们发现与MIS18BP1密切相关的基因在生物过程中主要与细胞周期、染色体分离和DNA修复相关。转染后,我们发现T24的增殖能力明显降低。跨井运移和划痕实验表明,运移减少。同时,下调MIS18BP1导致细胞凋亡增加。此外,在mis18bp1下调的T24中,P53、BAX和Cleaved Casepase-3增加,而BCL2蛋白减少。经聚氰菊酯-α处理后,细胞增殖抑制表型恢复。MIS18BP1过表达可能与BCa患者预后不良有关。MIS18BP1可能与BC细胞的凋亡和增殖有关。这一过程可能通过P53信号通路介导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MIS18BP1 promotes bladder cancer cell proliferation and growth via inactivating P53 signaling pathway.

MIS18 bonding protein 1 (MIS18BP1) is a subunit of MIS18 complex, accumulated specifically at telophase-G1 centromere and regulated apoptosis, proliferation and migration in cancer cells. The mechanisms about how MIS18BP1 regulate Bladder Cancer (BCa) cell development have not been previously unknown. We analyzed MIS18BP1 differential expression in BCa by The Cancer Genome Atlas (TCGA), Gene-Expression Omnibus (GEO) and Universal Protein database. The expression of MIS18BP1 mRNA was tested using qRT-PCR. The expression of MIS18BP1 protein was examined by western blot and immunohistochemistry (IHC) staining. T24 cells were transfected with an LV -MIS18BP1 -RNAi vector to decrease the MIS18BP1 expression. We used a series of experiments to detect the survival, proliferation and migration of T24. The apoptosis was analyzed by Flow cytometry assays. The expression of P53, BAX and Cleaved Casepase-3 was detected by western blot. P53 apoptosis-related proteins, proliferation and migration of cells were analyzed before and after treatment with P53 inhibitors. The expression of MIS18BP1 was higher in BCa tissues compared with control group. Its expression was in relation to clinical stage, depth of invasion and lymph node metastasis. We found that genes closely related to MIS18BP1 are mainly associated with cell cycle, chromosome separation and DNA repair in biological processes. After transfection, we found the proliferative capacity of T24 was significantly reduced. Transwell migration and scratch experiment demonstrated decreased migration. Meanwhile, downregulation of MIS18BP1 resulted in an increase in cell apoptosis. In addition, P53, BAX and Cleaved Casepase-3 were increased, whereas BCL2 protein was decreased in the MIS18BP1-downregulated T24. After treatment with Pifithrin-α, the phenotype of cell proliferation inhibition was restored. MIS18BP1 overexpression may be regulated to poor prognosis in BCa patients. MIS18BP1 may associated with cell apoptosis and proliferation in BC cells. This process may be mediated by P53 signal pathway.

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来源期刊
Medical Oncology
Medical Oncology 医学-肿瘤学
CiteScore
4.20
自引率
2.90%
发文量
259
审稿时长
1.4 months
期刊介绍: Medical Oncology (MO) communicates the results of clinical and experimental research in oncology and hematology, particularly experimental therapeutics within the fields of immunotherapy and chemotherapy. It also provides state-of-the-art reviews on clinical and experimental therapies. Topics covered include immunobiology, pathogenesis, and treatment of malignant tumors.
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