Circ-LAMP1 promotes T-cell lymphoblastic lymphoma progression via acting as a ceRNA for miR-615-5p to regulate DDR2 expression

Circular RNAs (circRNAs) act as pivotal functions in tumor progression. Nevertheless, the functions and mechanism of circRNAs in T-cell lymphoblastic lymphoma (T-LBL) remain unclear. In this work, we first screened the differentially expressed circRNAs between T-LBL tissues and normal infantile thym...

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Veröffentlicht in:Gene 2019-06, Vol.701, p.146-151
Hauptverfasser: Deng, Liling, Liu, Guohua, Zheng, Chanjuan, Zhang, Liwen, Kang, Yang, Yang, Fei
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Sprache:eng
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Zusammenfassung:Circular RNAs (circRNAs) act as pivotal functions in tumor progression. Nevertheless, the functions and mechanism of circRNAs in T-cell lymphoblastic lymphoma (T-LBL) remain unclear. In this work, we first screened the differentially expressed circRNAs between T-LBL tissues and normal infantile thymus and circ-LAMP1 was identified the highest expressed circRNA in cancerous tissues. qRT-PCR further verified its upregulation in T-LBL tissues and cell lines. Cell counting kit-8 (CCK-8) experiment proved the cell proliferation-promoting role of circ-LAMP1. This effect is partially dependent on its inhibition on cell apoptosis proved by flow cytometric assay. Dual-luciferase reporter system further identified that miR-615-5p could be sponged by circ-LAMP1 and discoidin domain receptor tyrosine kinase 2 (DDR2) 3′-UTR is the direct target of miR-615-5p. Rescue assays demonstrated that the biological function of circ-LAMP1 is partly attributed to the modulation of miR-615-5p/DDR2 signaling. In summary, these findings documented that circ-LAMP1 might be an oncogene in T-LBL, which might be useful in developing promising therapies for T-LBL. •Circ-LAMP1 is overexpressed in T-LBL tissues and cell lines.•Circ-LAMP1 promotes cell proliferation by inhibiting cell apoptosis in T-LBL cells.•Circ-LAMP1 positively regulates DDR2, a target of miR-615-5p.•Circ-LAMP1 modulates cell growth and apoptosis by regulating miR-615-5p/DDR2 pathway in T-LBL.
ISSN:0378-1119
1879-0038
DOI:10.1016/j.gene.2019.03.052