Norel Salut, Yaser Gamallat, Sima Seyedi, Joema Felipe Lima, Sunita Ghosh, Tarek A Bismar
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Our data indicated low BAP1 nuclear expression in advanced and castrate-resistant disease (CRPCa). Furthermore, there was a significant difference between high and low BAP1 nuclear expression relative to the patient's clinical outcome. In the present cohort, decreased BAP1 intensity exhibited a significant association with unfavorable overall survival (OS) (HR 2.31, CI: 1.38-3.86, <i>p</i> = 0.001) and cause-specific survival (CSS) (HR 2.44, CI: 1.24-4.78, <i>p</i> = 0.01). Additionally, this association was more pronounced when low BAP1 expression (high risk) was combined with other common PCa genomic alterations such as phosphatase and tensin homolog (PTEN) loss or ETS-related gene (ERG)-positive cases, resulting in higher unfavorable OS and CSS. Conversely, high BAP1 nuclear expression (moderate and high intensity) combined with no ERG expression or PTEN (moderate or high expression), p53 (wild type), and androgen receptor (AR) (low/moderate intensity) showed better association with higher survival rates. All these data support the notion that BAP1 functions as a tumor suppressor. 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引用次数: 0
摘要
前列腺癌(PCa)在西方社会被列为影响男性的头号癌症之一。brca1相关蛋白1 (BAP1)在包括前列腺癌在内的多种癌症中表达具有显著意义。寻找能够更好地对前列腺癌患者进行风险分层和疾病进展预测的预后模型仍然是主要的临床需求。我们的数据显示,核BAP1表达与癌症临床结果和其他生物标志物最相关。数据证实BAP1核表达降低与肿瘤侵袭性和预后不良有关。我们评估了202例BAP1的表达,包括晚期和去势抵抗性PCa (CRPCa)。我们的数据表明,BAP1核表达在晚期和去势抵抗性疾病(CRPCa)中较低。此外,BAP1核高表达与低表达与患者临床预后有显著差异。在本队列中,BAP1强度降低与不利的总生存率(OS) (HR 2.31, CI: 1.38-3.86, p = 0.001)和病因特异性生存率(CSS) (HR 2.44, CI: 1.24-4.78, p = 0.01)显著相关。此外,当BAP1低表达(高风险)与其他常见PCa基因组改变(如磷酸酶和紧张素同源物(PTEN)缺失或ets相关基因(ERG)阳性)合并时,这种关联更为明显,导致更高的不利OS和CSS。相反,BAP1高核表达(中等和高强度)与ERG或PTEN(中等或高表达)、p53(野生型)和雄激素受体(AR)(低/中强度)无表达合并,与更高的生存率有更好的相关性。所有这些数据都支持BAP1作为肿瘤抑制因子的观点。将BAP1状态与其他基因组改变结合起来,可以更全面地了解疾病的侵袭性。
Unraveling the Prognostic Significance of BRCA1-Associated Protein 1 (BAP1) Expression in Advanced and Castrate-Resistant Prostate Cancer.
Prostate cancer (PCa) is ranked as one of the top cancers affecting men in Western societies. BRCA1-associated protein 1 (BAP1) expression significance has been observed in various cancers, including prostate cancer. The search for prognostic models allowing better risk stratification and prediction of disease progression in prostate cancer patients is still of major clinical need. Our data showed that nuclear BAP1 expression is the most associated with cancer clinical outcomes and other biomarkers. The data confirmed that decreased BAP1 nuclear expression is linked to aggressive tumors and poorer prognosis. We assessed BAP1 expression in 202 cases, including advanced and castrate-resistant PCa (CRPCa). Our data indicated low BAP1 nuclear expression in advanced and castrate-resistant disease (CRPCa). Furthermore, there was a significant difference between high and low BAP1 nuclear expression relative to the patient's clinical outcome. In the present cohort, decreased BAP1 intensity exhibited a significant association with unfavorable overall survival (OS) (HR 2.31, CI: 1.38-3.86, p = 0.001) and cause-specific survival (CSS) (HR 2.44, CI: 1.24-4.78, p = 0.01). Additionally, this association was more pronounced when low BAP1 expression (high risk) was combined with other common PCa genomic alterations such as phosphatase and tensin homolog (PTEN) loss or ETS-related gene (ERG)-positive cases, resulting in higher unfavorable OS and CSS. Conversely, high BAP1 nuclear expression (moderate and high intensity) combined with no ERG expression or PTEN (moderate or high expression), p53 (wild type), and androgen receptor (AR) (low/moderate intensity) showed better association with higher survival rates. All these data support the notion that BAP1 functions as a tumor suppressor. Integrating BAP1 status with other genomic alterations offers a more comprehensive understanding of disease aggressiveness.
期刊介绍:
Biology (ISSN 2079-7737) is an international, peer-reviewed, quick-refereeing open access journal of Biological Science published by MDPI online. It publishes reviews, research papers and communications in all areas of biology and at the interface of related disciplines. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.