Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Chalubinskiego 1, 50-368 Wroclaw, Poland.
Br J Dermatol. 2012 Feb;166(2):331-6. doi: 10.1111/j.1365-2133.2011.10669.x. Epub 2012 Jan 9.
MicroRNAs are small noncoding RNA molecules involved in the regulation of various physiological and pathological processes. Altered expression of different microRNAs has been observed in both solid tumours and haematological malignancies.
To investigate expression of several microRNAs in early and advanced mycosis fungoides (MF).
Biopsies were obtained from 43 patients with MF (18 early MF and 25 advanced MF) and 23 healthy volunteers. After microRNA isolation, reverse transcriptase reactions were performed, followed by cDNA amplification. The following microRNAs were analysed: miR-15a, miR-16, miR-155, let-7a, let-7d and let-7f. The relative amount of each microRNA was normalized according to the reference RNU48 level.
Among the microRNAs studied, only MiR-155 was found to be slightly overexpressed in MF compared with healthy controls. Early MF showed a higher level of all analysed microRNAs after normalization against RNU48 level. Furthermore, metastatic MF demonstrated lower concentrations of let-7a, let-7d and let-7f when compared with MF limited to the skin. The univariate survival analysis and multivariate Cox's regression model revealed that the level of let-7a expression was an independent prognostic indicator.
Altered expression of studied microRNAs and the differences between early and advanced MF may suggest that microRNAs play a significant role in MF pathogenesis. It seems that microRNAs could serve as potential therapeutic targets in the future.
MicroRNAs 是一种参与调控多种生理和病理过程的小非编码 RNA 分子。在实体瘤和血液恶性肿瘤中都观察到不同 MicroRNAs 的表达发生改变。
研究几种 MicroRNAs 在蕈样肉芽肿(MF)早期和晚期的表达情况。
从 43 例 MF 患者(18 例早期 MF 和 25 例晚期 MF)和 23 例健康志愿者中获取活检样本。MicroRNA 分离后,进行逆转录反应,随后进行 cDNA 扩增。分析以下 MicroRNAs:miR-15a、miR-16、miR-155、let-7a、let-7d 和 let-7f。每种 MicroRNA 的相对含量根据参照 RNU48 水平进行标准化。
在所研究的 MicroRNAs 中,只有 miR-155 在 MF 中与健康对照相比略有过表达。早期 MF 在标准化为 RNU48 水平后,所有分析的 MicroRNAs 水平更高。此外,转移性 MF 与皮肤局限的 MF 相比,let-7a、let-7d 和 let-7f 的浓度较低。单因素生存分析和多因素 Cox 回归模型显示,let-7a 表达水平是独立的预后指标。
研究的 MicroRNAs 的表达改变以及早期和晚期 MF 之间的差异表明 MicroRNAs 在 MF 的发病机制中发挥重要作用。MicroRNAs 似乎可以作为未来潜在的治疗靶点。