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Chromobox homolog 8 is a predictor of muscle invasive bladder cancer and promotes cell proliferation by repressing the p53 pathway

机译:Chromobox homolog 8是肌肉浸润性膀胱癌的预测因子并通过抑制p53途径促进细胞增殖

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摘要

Chromobox homolog 8 (CBX8), also known as human polycomb 8, is a repressor that maintains the transcriptionally repressive state in various cellular genes, and has been reported to promote tumorigenesis. In the present study, we examined CBX8 expression in eight pairs of muscle invasive bladder cancer tissues and adjacent non‐tumor tissues, and found that CBX8 was frequently upregulated in muscle invasive bladder cancer tissues when compared to adjacent non‐tumor tissues. Analysis showed that high expression of CBX8 in 152 muscle invasive bladder cancer specimens was associated with progression of the T, N, and M stages (P = 0.004, 0.005, <0.001, respectively). Furthermore, Kaplan–Meier survival analysis and log–rank test showed that muscle invasive bladder cancer patients with high CBX8 expression had a poor rate of overall survival (P < 0.001) and 5‐year recurrence‐free survival (P < 0.001) compared to patients with low CBX8 expression. High CBX8 expression predicted poor overall survival and 5‐year recurrence‐free survival in T and N stages of muscle invasive bladder cancer patients. Moreover, knockdown of CBX8 inhibited cell proliferation of urothelial carcinoma of the bladder both in vitro and in vivo. In addition, CBX8 depletion resulted in cell cycle delay of urothelial carcinoma cells of the bladder at the G2/M phase by the p53 pathway. The data suggest that high expression of CBX8 plays a critical oncogenic role in aggressiveness of urothelial carcinoma cells of the bladder through promoting cancer cell proliferation by repressing the p53 pathway, and CBX8 could be used as a novel predictor for muscle invasive bladder cancer patients.
机译:Chromobox homolog 8(CBX8),也称为人polycomb 8,是一种阻遏物,可在多种细胞基因中维持转录抑制状态,据报道可促进肿瘤发生。在本研究中,我们检查了八对肌肉浸润性膀胱癌组织和邻近的非肿瘤组织中的CBX8表达,发现与邻近的非肿瘤组织相比,CBX8在肌肉浸润性膀胱癌组织中经常被上调。分析表明,CBX8在152个浸润性膀胱癌标本中的高表达与T,N和M期的进展有关(分别为P = 0.004、0.005和<0.001)。此外,Kaplan–Meier生存分析和对数秩检验表明,与CBX8高表达的肌肉浸润性膀胱癌患者相比,其总生存率(P <0.001)和5年无复发生存率(P <0.001) CBX8表达低的患者。 CBX8高表达预测肌肉浸润性膀胱癌患者在T和N期的总生存期和5年无复发生存期。而且,在体外和体内,敲低CBX8均抑制膀胱尿路上皮癌的细胞增殖。此外,CBX8耗竭通过p53途径导致了G2 / M期膀胱尿路上皮癌细胞的细胞周期延迟。数据表明,CBX8的高表达通过抑制p53途径促进癌细胞的增殖,从而在膀胱尿路上皮癌细胞的侵袭中起着关键的致癌作用,并且CBX8可以用作肌肉浸润性膀胱癌患者的新型预测因子。

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