Non-coding RNAs in GI cancers: from cancer hallmarks to clinical utility

被引:164
|
作者
Dragomir, Mihnea Paul [1 ]
Kopetz, Scott [2 ]
Ajani, Jaffer A. [2 ]
Calin, George Adrian [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Expt Therapeut, Houston, TX 77054 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
COLORECTAL-CANCER; HEPATOCELLULAR-CARCINOMA; POTENTIAL BIOMARKER; CIRCULATING LNCRNAS; GENOMIC STABILITY; MISMATCH REPAIR; MICRORNAS; PLASMA; SERUM; INSTABILITY;
D O I
10.1136/gutjnl-2019-318279
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
One of the most unexpected discoveries in molecular oncology, in the last decades, was the identification of a new layer of protein coding gene regulation by transcripts that do not codify for proteins, the non-coding RNAs. These represent a heterogeneous category of transcripts that interact with many types of genetic elements, including regulatory DNAs, coding and other non-coding transcripts and directly to proteins. The final outcome, in the malignant context, is the regulation of any of the cancer hallmarks. Non-coding RNAs represent the most abundant type of hormones that contribute significantly to cell-to cell communication, revealing a complex interplay between tumour cells, tumour microenvironment cells and immune cells. Consequently, profiling their abundance in bodily fluids became a mainstream of biomarker identification. Therapeutic targeting of non-coding RNAs represents a new option for clinicians that is currently under development. This review will present the biology and translational value of three of the most studied categories on non-coding RNAs, the microRNAs, the long non-coding RNAs and the circular RNAs. We will also focus on some aspirational concepts that can help in the development of clinical applications related to non-coding RNAs, including using pyknons to discover new non-coding RNAs, targeting human-specific transcripts which are expressed specifically in the tumour cell and using non-coding RNAs to increase the efficiency of immunotherapy.
引用
收藏
页码:748 / 763
页数:16
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