Hatse Sigrid, Brouwers Barbara, Dalmasso Bruna, Laenen Annouschka, Kenis Cindy, Schöffski Patrick, Wildiers Hans
Laboratory of Experimental Oncology (LEO), Department of Oncology, KU Leuven, and Department of General Medical Oncology, University Hospitals Leuven, Leuven Cancer Institute, Leuven, Belgium.
Laboratory of Experimental Oncology (LEO), Department of Oncology, KU Leuven, and Department of General Medical Oncology, University Hospitals Leuven, Leuven Cancer Institute, Leuven, Belgium; Department of Internal Medicine, Istituto di Ricerca a Carattere Clinico e Scientifico (IRCCS), Azienda Ospedaliera Universitaria (AOU) San Martino Istituto Nazionale Tumori (IST), Genoa, Italy.
PLoS One. 2014 Oct 21;9(10):e110644. doi: 10.1371/journal.pone.0110644. eCollection 2014.
Circulating microRNAs (miRNAs) hold great promise as easily accessible biomarkers for diverse (patho)physiological processes, including aging. We have compared miRNA expression profiles in cell-free blood from older versus young breast cancer patients, in order to identify "aging miRNAs" that can be used in the future to monitor the impact of chemotherapy on the patient's biological age. First, we assessed 175 miRNAs that may possibly be present in serum/plasma in an exploratory screening in 10 young and 10 older patients. The top-15 ranking miRNAs showing differential expression between young and older subjects were further investigated in an independent cohort consisting of another 10 young and 20 older subjects. Plasma levels of miR-20a-3p, miR-30b-5p, miR106b, miR191 and miR-301a were confirmed to show significant age-related decreases (all p≤0.004). The remaining miRNAs included in the validation study (miR-21, miR-210, miR-320b, miR-378, miR-423-5p, let-7d, miR-140-5p, miR-200c, miR-374a, miR376a) all showed similar trends as observed in the exploratory screening but these differences did not reach statistical significance. Interestingly, the age-associated miRNAs did not show differential expression between fit/healthy and non-fit/frail subjects within the older breast cancer cohort of the validation study and thus merit further investigation as true aging markers that not merely reflect frailty.
循环微RNA(miRNA)作为多种(病理)生理过程(包括衰老)易于获取的生物标志物,具有巨大的潜力。我们比较了老年与年轻乳腺癌患者无细胞血液中的miRNA表达谱,以鉴定“衰老miRNA”,这些miRNA未来可用于监测化疗对患者生物学年龄的影响。首先,我们在10名年轻患者和10名老年患者的探索性筛查中评估了175种可能存在于血清/血浆中的miRNA。在由另外10名年轻患者和20名老年患者组成的独立队列中,进一步研究了在年轻和老年受试者之间显示差异表达的前15名miRNA。miR-20a-3p、miR-30b-5p、miR106b、miR191和miR-301a的血浆水平被证实显示出与年龄相关的显著下降(所有p≤0.004)。验证研究中包括的其余miRNA(miR-21、miR-210、miR-320b、miR-378、miR-423-5p、let-7d、miR-140-5p、miR-200c、miR-374a、miR376a)均显示出与探索性筛查中观察到的相似趋势,但这些差异未达到统计学显著性。有趣的是,在验证研究的老年乳腺癌队列中,与年龄相关的miRNA在健康/健康和不健康/虚弱的受试者之间未显示出差异表达,因此作为真正的衰老标志物值得进一步研究,而不仅仅反映虚弱。