| Literature DB >> 31814902 |
Liyang Dong1, Chao Ding1, Tingting Zheng1, Yanan Pu2, Jiameng Liu1, Wenzhe Zhang3, Fei Xue3, Ping Kang1, Yongbin Ma4, Xuefeng Wang1,3, Chaoming Mao1.
Abstract
Recent evidence has shown that long noncoding RNAs (lncRNAs) play major roles in tumorigenesis and cancer progression. The cancer genome atlas program (TCGA) database was used to screen colon adenocarcinoma (COAD)-related differentially expressed lncRNAs, which revealed that lncRNA ELFN1-AS1 was highly expressed in COAD. This study aimed to explore the regulatory role of ELFN1-AS1 in COAD and construct a gene delivery system based on extracellular vesicles (EVs). We found that ELFN1-AS1 levels were obviously increased in COAD patients and COAD tumor cells. Knockdown of ELFN1-AS1 expression by siRNA inhibited COAD cell proliferation and migration. Moreover, silencing ELFN1-AS1 significantly reduced the activation of extracellular signal-regulated protein kinase (Erk), up-regulated the protein expression of E-cadherin and down-regulated vimentin. In addition, we treated human umbilical cord mesenchymal stem cells (hUCMSCs) with siRNA-ELFN1-AS1 and found that EVs from siRNA-ELFN1-AS1-treated hUCMSCs could inhibit COAD cell proliferation and migration in vitro. These findings suggested that ELFN1-AS1 could promote the progression of COAD and that hUCMSC-EVs might be an attractive vehicle for the clinical administration of lncRNA-specific siRNAs in patients with COAD. AJTREntities:
Keywords: ELFN1-AS1; colon adenocarcinoma; extracellular vesicles; human umbilical cord mesenchymal stem cells
Year: 2019 PMID: 31814902 PMCID: PMC6895508
Source DB: PubMed Journal: Am J Transl Res ISSN: 1943-8141 Impact factor: 4.060