Small extracellular vesicle non-coding RNAs in pancreatic cancer: molecular mechanisms and clinical implications

被引:44
|
作者
Reese, Moritz [1 ]
Dhayat, Sameer A. [1 ]
机构
[1] Univ Hosp Muenster, Dept Gen Visceral & Transplant Surg, Albert Schweitzer Campus 1 W1, D-48149 Munster, Germany
关键词
Pancreatic cancer; Pancreatic ductal adenocarcinoma; Exosome; Small extracellular vesicle; Non-coding RNA; MicroRNA; Long non-coding RNA; Circular RNA; TUMOR-ASSOCIATED MACROPHAGE; REGULATORY T-CELLS; PHASE-III TRIAL; DENDRITIC CELLS; IN-VIVO; EXOSOMAL MICRORNA-21; POTENTIAL BIOMARKER; ANTITUMOR-ACTIVITY; NORMAL FIBROBLASTS; DELIVERY PLATFORM;
D O I
10.1186/s13045-021-01149-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancer has the worst prognosis among common tumors which is attributed to its aggressive phenotype, diagnosis at advanced, inoperable stages, and resistance to systemic therapy. Non-coding RNAs (ncRNAs) such as microRNAs, long non-coding RNAs, and circular RNAs have been established as important regulators of gene expression and their deregulation has been implicated in multiple diseases and foremost cancer. In the tumor microenvironment, non-coding RNAs can be distributed among cancer cells, stromal cells, and immune cells via small extracellular vesicles (sEVs), thereby facilitating intercellular communication and influencing major cancer hallmarks such as angiogenesis, evasion of the immune system, and metastatic dissemination. Furthermore, sEV-ncRNAs have shown promising potential as liquid biopsies with diagnostic and prognostic significance. In this review, we summarize the role of sEVs as carriers of ncRNAs and underlying molecular mechanisms in pancreatic cancer. Moreover, we review the potential of sEV-ncRNAs as biomarkers and highlight the suitability of sEVs as delivery vehicles for ncRNA-based cancer therapy.
引用
收藏
页数:27
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