The dual role of microRNA-9 in gastrointestinal cancers: oncomiR or tumor suppressor?

被引:11
|
作者
Bahrami, Afsane [1 ,2 ]
Jafari, Amirsajad [3 ]
Ferns, Gordon A. [4 ]
机构
[1] Mashhad Univ Med Sci, Clin Res Dev Unit, Fac Med, Akbar Hosp, Mashhad, Razavi Khorasan, Iran
[2] Mashhad Univ Med Sci, Imam Reza Hosp, Fac Med, Clin Res Dev Unit, Mashhad, Razavi Khorasan, Iran
[3] Shiraz Univ, Sch Vet Med, Dept Basic Sci, Shiraz, Iran
[4] Brighton & Sussex Med Sch, Div Med Educ, Brighton BN1 9PH, Sussex, England
关键词
Cyclin D1; CXCR-4; CDX2; Colorectal cancer; LncRNA; EPITHELIAL-MESENCHYMAL TRANSITION; LONG NONCODING RNA; COLORECTAL-CANCER; CELL-PROLIFERATION; GASTRIC-CANCER; NASOPHARYNGEAL CARCINOMA; DOWN-REGULATION; HEPATOCELLULAR-CARCINOMA; POTENTIAL BIOMARKER; MIR-9-3P SUPPRESSES;
D O I
10.1016/j.biopha.2021.112394
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
microRNA are noncoding endogenous RNAs of similar to 25-nucleotide, involved in RNA silencing and controlling of cell function. Recent evidence has highlighted the important role of various in the biology of human cancers. miR-9 is a highly conserved microRNA and abnormal regulation of miR-9 expression has various impacts on disease pathology. miR-9 may play a dual tumor-suppressive or oncomiR activity in several cancers. There have been conflicting reports concerning the role of miR-9 in gastrointestinal cancers. Several signaling pathways including PDK/AKT, Hippo, Wnt/beta-catenin and PDGFRB axes are affected by miR-9 in suppressing proliferation, invasion and metastasis of tumor cells. Oncogenic miR-9 triggers migration, metastasis and clinic-pathological characteristics of patients with gastrointestinal malignancy by targeting various enzymes and transcription factors such as E-cadherin, HK2, LMX1A, and CDX2. On the other hand, long non-coding RNAs and circular RNAs can modulate miR-9 expression in human cancers. In this review, we aimed to summarize recent findings about the potential value of miR-9 in gastrointestinal tumors, that include: screening, prognostic and treatment.
引用
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页数:9
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