Lab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Key Lab of Molecular Cancer Biology, Yunnan Education Department, Kunming 650091, China.
Int J Mol Sci. 2018 Sep 17;19(9):2791. doi: 10.3390/ijms19092791.
Colorectal cancer (CRC) is responsible for one of the major cancer incidence and mortality worldwide. It is well known that MicroRNAs (miRNAs) play vital roles in maintaining the cell development and other physiological processes, as well as, the aberrant expression of numerous miRNAs involved in CRC progression. MiRNAs are a class of small, endogenous, non-coding, single-stranded RNAs that bind to the 3'-untranslated region (3'-UTR) complementary sequences of their target mRNA, resulting in mRNA degradation or inhibition of its translation as a post-transcriptional regulators. Moreover, miRNAs also can target the long non-coding RNA (lncRNA) to regulate the expression of its target genes involved in proliferation and metastasis of CRC. The functions of these dysregulated miRNAs appear to be context specific, with evidence of having a dual role in both oncogenes and tumor suppression depending on the cellular environment in which they are expressed. Therefore, the unique expression profiles of miRNAs relate to the diagnosis, prognosis, and therapeutic outcome in CRC. In this review, we focused on several oncogenic and tumor-suppressive miRNAs specific to CRC, and assess their functions to uncover the molecular mechanisms of tumor initiation and progression in CRC. These data promised that miRNAs can be used as early detection biomarkers and potential therapeutic target in CRC patients.
结直肠癌(CRC)是全球主要癌症发病率和死亡率的原因之一。众所周知,MicroRNAs(miRNAs)在维持细胞发育和其他生理过程中起着至关重要的作用,并且许多参与 CRC 进展的miRNAs 的表达异常。miRNAs 是一类小的、内源性、非编码、单链 RNA,可与靶 mRNA 的 3'非翻译区(3'-UTR)互补序列结合,导致 mRNA 降解或抑制其翻译,作为转录后调节因子。此外,miRNAs 还可以靶向长非编码 RNA(lncRNA)来调节其靶基因的表达,这些靶基因参与 CRC 的增殖和转移。这些失调的 miRNAs 的功能似乎是特定于上下文的,有证据表明它们在肿瘤抑制基因和癌基因中具有双重作用,这取决于它们表达的细胞环境。因此,miRNAs 的独特表达谱与 CRC 的诊断、预后和治疗结果有关。在这篇综述中,我们集中讨论了几种特定于 CRC 的致癌和肿瘤抑制 miRNAs,并评估了它们的功能,以揭示 CRC 中肿瘤起始和进展的分子机制。这些数据表明,miRNAs 可以作为 CRC 患者早期检测的生物标志物和潜在的治疗靶点。