Center for Cancer Research, NCI, Bethesda, MD, 20892, USA.
Leidos Biomedical Research, Inc., Frederick, MD, 21702-1201, USA.
BMC Cancer. 2020 May 6;20(1):388. doi: 10.1186/s12885-020-06901-6.
Esophageal squamous cell carcinoma (ESCC) is a leading cause of cancer death worldwide and in China. We know miRNAs influence gene expression in tumorigenesis, but it is unclear how miRNAs affect gene expression or influence survival at the genome-wide level in ESCC.
We performed miRNA and mRNA expression arrays in 113 ESCC cases with tumor/normal matched tissues to identify dysregulated miRNAs, to correlate miRNA and mRNA expressions, and to relate miRNA and mRNA expression changes to survival and clinical characteristics.
Thirty-nine miRNAs were identified whose tumor/normal tissue expression ratios showed dysregulation (28 down- and 11 up-regulated by at least two-fold with P < 1.92E-04), including several not previously reported in ESCC (miR-885-5p, miR-140-3p, miR-708, miR-639, miR-596). Expressions of 16 miRNAs were highly correlated with expressions of 195 genes (P < 8.42E-09; absolute rho values 0.51-0.64). Increased expressions of miRNA in tumor tissue for both miR-30e* and miR-124 were associated with increased survival (P < 0.05). Similarly, nine probes in eight of 818 dysregulated genes had RNA expression levels that were nominally associated with survival, including NF1, ASXL1, HSPA4, TGOLN2, BAIAP2, EZH2, CHAF1A, SUPT7L.
Our characterization and integrated analysis of genome-wide miRNA and gene expression in ESCC provides insights into the expression of miRNAs and their relation to regulation of RNA targets in ESCC tumorigenesis, and suggest opportunities for the future development of miRs and mRNAs as biomarkers for early detection, diagnosis, and prognosis in ESCC.
食管鳞状细胞癌(ESCC)是全世界和中国癌症死亡的主要原因。我们知道 miRNA 会影响肿瘤发生中的基因表达,但尚不清楚 miRNA 如何在全基因组水平上影响基因表达或影响生存。
我们对 113 例肿瘤/正常配对组织的 ESCC 病例进行了 miRNA 和 mRNA 表达谱分析,以鉴定失调的 miRNA,相关 miRNA 和 mRNA 表达,并将 miRNA 和 mRNA 表达变化与生存和临床特征相关联。
确定了 39 个 miRNA,其肿瘤/正常组织表达比率显示失调(28 个下调,11 个上调至少两倍,P<1.92E-04),包括一些以前未在 ESCC 中报道的 miRNA(miR-885-5p、miR-140-3p、miR-708、miR-639、miR-596)。16 个 miRNA 的表达与 195 个基因的表达高度相关(P<8.42E-09;绝对 rho 值 0.51-0.64)。肿瘤组织中 miRNA-30e*和 miR-124 的表达增加与生存时间延长相关(P<0.05)。同样,在 818 个失调基因中有九个探针在 818 个失调基因中的八个基因中其 RNA 表达水平与生存呈名义相关,包括 NF1、ASXL1、HSPA4、TGOLN2、BAIAP2、EZH2、CHAF1A、SUPT7L。
我们对 ESCC 中全基因组 miRNA 和基因表达的特征描述和综合分析,深入了解了 miRNA 的表达及其与 ESCC 肿瘤发生中 RNA 靶标的调控关系,并为未来 miRNA 和 mRNA 作为 ESCC 早期检测、诊断和预后的生物标志物的开发提供了机会。