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含溴结构域蛋白7在前列腺癌中的临床意义及其与肿瘤进展的关系。

Clinical significance of bromodomain-containing protein 7 and its association with tumor progression in prostate cancer.

作者信息

Liang Yong, Dong Baiping, Shen Jiangwei, Ma Caosheng, Ma Zhongping

机构信息

Department of Urology Surgery, Caoxian People's Hospital, Heze, Shandong 274400, P.R. China.

出版信息

Oncol Lett. 2019 Jan;17(1):849-856. doi: 10.3892/ol.2018.9665. Epub 2018 Nov 5.

Abstract

Prostate cancer (PCa) is a common malignancy in males. The current study assessed the clinical significance of bromodomain-containing protein 7 (BRD7) and its association with PCa tumor progression. Serum and tissue expression levels of BRD7 were analyzed by reverse transcription-quantitative polymerase chain reaction. Receiver operating characteristic (ROC) analysis was used to evaluate the diagnostic value of BRD7. Kaplan-Meier survival analysis and Cox regression analysis were performed to assess the prognostic performance of BRD7. The association of BRD7 with cell behavior was investigated by transfection with a pcDNA3.1-BRD7 vector. The results revealed that serum and tissue BRD7 expression levels were significantly decreased in PCa samples compared with normal controls (P<0.001). BRD7 expression was significantly associated with the pathological stage (P=0.037), lymph node metastasis (P=0.009) and TNM stage (P=0.010). An area under the ROC curve of 0.864 was obtained, with a sensitivity and specificity of 77.0 and 83.3%, respectively. Low BRD7 expression was significantly associated with a shorter survival time in both overall survival analysis (P=0.003) and cancer-specific survival analysis (P=0.029). Furthermore, BRD7 appeared to serve as an independent prognostic factor for PCa. The proliferation, migration and invasion of PCa cells were suppressed by BRD7 overexpression. In summary, downregulation of BRD7 in PCa may be involved in tumor progression and serve as an effective diagnostic and prognostic biomarker.

摘要

前列腺癌(PCa)是男性常见的恶性肿瘤。本研究评估了含溴结构域蛋白7(BRD7)的临床意义及其与PCa肿瘤进展的关系。通过逆转录定量聚合酶链反应分析BRD7的血清和组织表达水平。采用受试者工作特征(ROC)分析评估BRD7的诊断价值。进行Kaplan-Meier生存分析和Cox回归分析以评估BRD7的预后性能。通过用pcDNA3.1-BRD7载体转染研究BRD7与细胞行为的关系。结果显示,与正常对照相比,PCa样本中血清和组织BRD7表达水平显著降低(P<0.001)。BRD7表达与病理分期(P=0.037)、淋巴结转移(P=0.009)和TNM分期(P=0.010)显著相关。获得的ROC曲线下面积为0.864,敏感性和特异性分别为77.0%和83.3%。在总生存分析(P=0.003)和癌症特异性生存分析(P=0.029)中,低BRD7表达均与较短的生存时间显著相关。此外,BRD7似乎是PCa的独立预后因素。BRD7过表达抑制了PCa细胞的增殖、迁移和侵袭。总之,PCa中BRD7的下调可能参与肿瘤进展,并作为一种有效的诊断和预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e53/6313008/a1e35b3c7728/ol-17-01-0849-g00.jpg

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