LncRNA PSMA3-AS1在前列腺癌中的预后价值及其潜在调控机制

IF 2.5 3区 生物学
Muyang Cao, Jin Li, Jianbin Zhang, Wenlong Lu
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引用次数: 0

摘要

目的:前列腺腺癌(PRAD)早期无症状,多数患者诊断为晚期,预后较差。因此,需要一种有效的预后标志物来改善PRAD的预后。方法:共纳入128例PRAD患者。RT-qPCR检测组织中PSMA3-AS1和miR-29a-3p的表达。然后用CCK-8和Transwell试验评估前列腺癌细胞系的增殖、迁移和侵袭能力。DLR分析证实了PSMA3-AS1与miR-29a-3p之间的结合关系。使用Kaplan-Meier绘图图曲线分析PRAD患者的5年预后。结果:PSMA3-AS1在PRAD组织中高表达,高表达患者5年生存率较差。相比之下,miR-29a-3p在PRAD组织中表达较低。PSMA3-AS1靶向结合miR-29a-3p,且水平呈负相关。敲低PSMA3-AS1可提高miR-29a-3p水平,减缓PRAD细胞系的增殖,抑制其迁移和侵袭能力。结论:高水平的PSMA3-AS1与患者的不良预后密切相关,有望作为PRAD的预后标志物。此外,PSMA3-AS1敲低可提高miR-29a-3p水平,降低癌细胞的生理活性。因此,调节PSMA3-AS1/miR-29a-3p轴的表达可能影响PRAD的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic value of LncRNA PSMA3-AS1 in prostate cancer and its potential regulatory mechanism.

Objective: Prostate adenocarcinoma (PRAD) is asymptomatic in the early stages and most patients are diagnosed at an advanced stage, which leads to a poor prognosis. Therefore, an effective prognostic marker is required to improve PRAD prognosis.

Methods: A total of 128 patients with PRAD were included in the study. PSMA3-AS1 and miR-29a-3p expression in tissues was detected using RT-qPCR. CCK-8 and Transwell assays were then used to evaluate the proliferative, migratory, and invasive capacities of prostate cancer cell lines. A DLR assay confirmed the binding relationship between PSMA3-AS1 and miR-29a-3p. The five-year prognosis of PRAD patients was analyzed using a Kaplan-Meier plotter curve.

Results: PSMA3-AS1 was highly expressed in PRAD tissues, and patients with high expression had poor 5-year survival. In contrast, miR-29a-3p was poorly expressed in PRAD tissues. PSMA3-AS1 bound to miR-29a-3p in a targeted manner and the levels showed a negative correlation. Knocking down PSMA3-AS1 could increase the level of miR-29a-3p and slow the proliferation of PRAD cell lines, as well as inhibiting their migration and invasion ability.

Conclusion: A high level of PSMA3-AS1 was strongly linked to a poor prognosis for patients and is expected to serve as a prognostic marker for PRAD. Furthermore, PSMA3-AS1 knockdown increased the level of miR-29a-3p and reduced the physiological activity of cancer cells. Therefore, regulating the expression of the PSMA3-AS1/miR-29a-3p axis could influence PRAD development.

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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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