Narasimhan Ashok, Ghosh Sunita, Stretch Cynthia, Greiner Russell, Bathe Oliver F, Baracos Vickie, Damaraju Sambasivarao
Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
Department of Oncology, University of Alberta, Edmonton, Alberta, Canada.
J Cachexia Sarcopenia Muscle. 2017 Jun;8(3):405-416. doi: 10.1002/jcsm.12168. Epub 2017 Jan 6.
MicroRNAs (miRs) are small non-coding RNAs that regulate gene (mRNA) expression. Although the pathological role of miRs have been studied in muscle wasting conditions such as myotonic and muscular dystrophy, their roles in cancer cachexia (CC) are still emerging.
The objectives are (i) to profile human skeletal muscle expressed miRs; (ii) to identify differentially expressed (DE) miRs between cachectic and non-cachectic cancer patients; (iii) to identify mRNA targets for the DE miRs to gain mechanistic insights; and (iv) to investigate if miRs show potential prognostic and predictive value.
Study subjects were classified based on the international consensus diagnostic criteria for CC. Forty-two cancer patients were included, of which 22 were cachectic cases and 20 were non-cachectic cancer controls. Total RNA isolated from muscle biopsies were subjected to next-generation sequencing.
A total of 777 miRs were profiled, and 82 miRs with read counts of ≥5 in 80% of samples were retained for analysis. We identified eight DE miRs (up-regulated, fold change of ≥1.4 at P < 0.05). A total of 191 potential mRNA targets were identified for the DE miRs using previously described human skeletal muscle mRNA expression data (n = 90), and a majority of them were also confirmed in an independent mRNA transcriptome dataset. Ingenuity pathway analysis identified pathways related to myogenesis and inflammation. qRT-PCR analysis of representative miRs showed similar direction of effect (P < 0.05), as observed in next-generation sequencing. The identified miRs also showed prognostic and predictive value.
In all, we identified eight novel miRs associated with CC.
微小RNA(miR)是调节基因(mRNA)表达的小型非编码RNA。尽管miR在诸如强直性肌营养不良和肌肉萎缩症等肌肉萎缩病症中的病理作用已得到研究,但其在癌症恶病质(CC)中的作用仍在不断显现。
目标是(i)分析人类骨骼肌中表达的miR;(ii)鉴定恶病质和非恶病质癌症患者之间差异表达(DE)的miR;(iii)鉴定DE miR的mRNA靶标以获得机制性见解;以及(iv)研究miR是否具有潜在的预后和预测价值。
根据CC的国际共识诊断标准对研究对象进行分类。纳入了42例癌症患者,其中22例为恶病质病例,20例为非恶病质癌症对照。从肌肉活检中分离的总RNA进行下一代测序。
共分析了777个miR,保留了80%样本中读数计数≥5的82个miR用于分析。我们鉴定出8个DE miR(上调,在P<0.05时倍数变化≥1.4)。使用先前描述的人类骨骼肌mRNA表达数据(n = 90)为DE miR鉴定了总共191个潜在的mRNA靶标,其中大多数也在独立的mRNA转录组数据集中得到证实。 Ingenuity通路分析确定了与肌生成和炎症相关的通路。代表性miR的qRT-PCR分析显示出与下一代测序中观察到的相似的效应方向(P<0.05)。鉴定出的miR还显示出预后和预测价值。
总之,我们鉴定出8个与CC相关的新型miR。