首页> 美国卫生研究院文献>Turkish Journal of Urology >The Combined Effect of Downregulated RB1 and Overexpressed lncRNA SSTRS-AS1 on Prediction Time to Castration-Resistant Prostate Cancer: Indonesian Cohort Studies
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The Combined Effect of Downregulated RB1 and Overexpressed lncRNA SSTRS-AS1 on Prediction Time to Castration-Resistant Prostate Cancer: Indonesian Cohort Studies

机译:下调 RB1 和过表达 lncRNA SSTRS-AS1 对去势抵抗性前列腺癌预测时间的综合影响:印度尼西亚队列研究

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摘要

Objective: Identifying the mechanism underlying the initiation and development of castration-resistant prostate cancer remains challenging. Time to castration-resistant prostate cancer is defined by prostate-­specific antigen progression and may represent a risk factor for developing immune alterations with a negative prognostic role in the overall survival of patients with prostate cancer. This study aimed to evaluate the combined effect of downregulated RB1 and overexpressed SSTR5-AS1 as biomarkers for predicting time to castration-resistant prostate cancer.Material and Methods: The clinical and pathological data of patients with prostate cancer were collected retrospectively. Between 2015 and 2019, a total of 36 patients who received castration were included. Expressions of mRNA of RB1 and SSTR5-AS1 from primary tumors were quantified using quantitative real-time polymerase chain reaction. Patients were divided into 2 groups: the first group consisted of patients with Rb1 expression lower than the median and expression of SSTRS5-AS1 higher than the median, and the second group consisted of all the other patients. This study was conducted in compliance with the latest Helsinki Declaration and registered on Elsevier International Standard Randomized Controlled trial number registry.Results: In this study, patients with both downregulated RB1 and overexpressed Long non-coding RNAs (lncRNA) SSTR5-AS1 showed shorter time to castration-resistant prostate cancer (mean 23.6 ± 3.3 months) compared to other groups (mean 38.3 ± 4.9 months) (log-rank test, P = .028).Conclusion: The combination of downregulation of RB1 and overexpression of SSTR5-AS1 is a strong predictor of shorter time to castration-resistant prostate cancer in the Indonesian population. Additionally, patients with International Society of Urological Pathology (ISUP) score >4 did not demonstrate this predictive value on time to castration-resistant prostate cancer.
机译:目的: 确定去势抵抗性前列腺癌发生和发展的潜在机制仍然具有挑战性。去势抵抗性前列腺癌的时间由前列腺特异性抗原进展定义,可能代表发生免疫改变的危险因素,对前列腺癌患者的总生存期具有负面预后作用。本研究旨在评估下调 RB1 和过表达 SSTR5-AS1 作为预测去势抵抗性前列腺癌时间的生物标志物的综合效应。材料和方法: 回顾性收集前列腺癌患者的临床和病理资料。2015 年至 2019 年期间,共纳入 36 例接受去势的患者。使用定量实时聚合酶链反应定量原发肿瘤 RB1 和 SSTR5-AS1 mRNA 的表达。将患者分为 2 组: 第一组由 Rb1 表达低于中位数且 SSTRS5-AS1 表达高于中位数的患者组成,第二组由所有其他患者组成。本研究是根据最新的赫尔辛基宣言进行的,并在爱思唯尔国际标准随机对照试验编号注册处注册。结果: 在这项研究中,RB1 下调和过表达长链非编码 RNA (lncRNA) SSTR5-AS1 的患者患去势抵抗性前列腺癌的时间更短 (平均 23.6 ± 3。3 个月)与其他组 (平均 38.3 ± 4.9 个月) 相比 (对数秩检验,P = .028)。结论: RB1 下调和 SSTR5-AS1 过表达的组合是印度尼西亚人群中去势抵抗性前列腺癌时间缩短的强预测因子。此外,国际泌尿外科病理学会 (ISUP) 评分为 >4 分的患者未证明对去势抵抗性前列腺癌时间的预测价值。

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