MicroRNA95 May Be Involved in Oligometastatic Prostate Cancer

C. F. Albiach, E. Aranda, Alfonso Gomez Iturriaga-Piña, Amalia Ruiz, F. L. Campos, M. P. Martínez, R. Gómez, M. A. López, V. Fernandez, A. J. C. Moreno, Susana Ors, E. Flores, F. G. Piñón
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Abstract

The oligometastatic status in the prostate is a new entity of metastatic patients in which their treatment allows to improve survival over standard treatments. There are several theories about their biological origin, one of them being alterations in the expression of miRNas This. was a retrospective multicentre study undertaken in patients with oligometastatic prostate cancer who were diagnosed and treated at one of 7 different Spanish healthcare centres. METHODS: The study included 22 patients; healthy and primary tumour biopsy tissue was analysed in 7+2 of them in order to determine if they had a characteristic microRNA expression profile. We quantified the expression of the following miRNAs: mir‑200a, mir‑200b, mir‑200c, mir‑210, mir‑95, mir‑96, mir‑654‑3p, mir‑543‑3p, mir‑21, mir‑16‑5p, mir‑191‑5p, and mir‑93‑5p, with the latter three being endogenous‑expression controls. RESULTS: Our results show that miRNA95, and to a lesser extent, miRNA654‑3p, were significantly underexpressed (or their expression was suppressed) in tumour tissue samples compared to normal perilesional tissue in all our patients; miRNA95 was underexpressed in 67% of the patients in our sample However, we detected no relationship between miRNA95 expression and the Gleason scores obtained for our patients. CONCLUSIONS: The simple size in our series are limited, but they do allow us to infer that there could be a specific miRNA expression signature in oligometastatic patients with prostate cancer, which may be of great interest in the development of future clinical trials and subsequent studies.
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MicroRNA95可能与少转移性前列腺癌有关
前列腺的低转移状态是转移性患者的一个新的实体,在这种情况下,他们的治疗可以比标准治疗提高生存率。关于它们的生物学起源有几种理论,其中一种是mirna表达的改变。是一项多中心回顾性研究,研究对象是在西班牙7个不同保健中心之一诊断和治疗的少转移性前列腺癌患者。方法:纳入22例患者;对其中7+2例患者的健康和原发肿瘤活检组织进行分析,以确定他们是否具有特征性的microRNA表达谱。我们量化了以下mirna的表达:mir‑200a、mir‑200b、mir‑200c、mir‑210、mir‑95、mir‑96、mir‑654‑3p、mir‑543‑3p、mir‑21、mir‑16‑5p、mir‑191‑5p和mir‑93‑5p,后三种mirna为内源性表达对照。结果:我们的研究结果显示,与所有患者的正常病变周围组织相比,miRNA95和较小程度上的miRNA654‑3p在肿瘤组织样本中显著低表达(或表达被抑制);在我们的样本中,67%的患者miRNA95表达不足。然而,我们没有发现miRNA95表达与我们的患者获得的Gleason评分之间的关系。结论:在我们的系列中,简单的大小是有限的,但它们确实使我们推断出在前列腺癌少转移患者中可能存在特定的miRNA表达特征,这可能对未来临床试验和后续研究的发展有很大的兴趣。
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