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E2F transcription factor 2-activated DLEU2 contributes to prostate tumorigenesis by upregulating serum and glucocorticoid-induced protein kinase 1.
- Source :
-
Cell death & disease [Cell Death Dis] 2022 Jan 24; Vol. 13 (1), pp. 77. Date of Electronic Publication: 2022 Jan 24. - Publication Year :
- 2022
-
Abstract
- Long noncoding RNAs (lncRNAs) participate in biological processes in multiple types of tumors. However, the regulatory patterns of lncRNAs in prostate cancer remain largely unclear. Here, we evaluated the expression and roles of the lncRNA DLEU2 in prostate cancer. Our results showed that DLEU2 was upregulated in advanced prostate cancer tissues. Patients with prostate cancer displaying high expression of DLEU2 had a poor prognosis. Moreover, we demonstrated that overexpression of DLEU2 facilitated the proliferation, migration, and invasion of prostate cancer in vitro. Mechanistically, DLEU2 promoted serum and glucocorticoid-induced protein kinase 1 (SGK1) expression by acting as an miR-582-5p sponge, and the transcription of DLEU2 was activated by the dysregulation of E2F transcription factor 2 (E2F2) expression in prostate cancer. Furthermore, knockdown of DLEU2 attenuated prostate cancer tumorigenesis in vivo. Notably, these findings suggested that E2F2-activated DLEU2 may function as a competing endogenous RNA to facilitate prostate cancer progression by targeting the miR-582-5p/SGK1 axis.<br /> (© 2022. The Author(s).)
- Subjects :
- Carcinogenesis genetics
Cell Line, Tumor
Cell Movement genetics
Cell Proliferation genetics
Cell Transformation, Neoplastic genetics
Gene Expression Regulation, Neoplastic
Humans
Immediate-Early Proteins metabolism
Male
MicroRNAs genetics
Prostate metabolism
Protein Serine-Threonine Kinases metabolism
E2F2 Transcription Factor genetics
Prostatic Neoplasms genetics
RNA, Long Noncoding genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2041-4889
- Volume :
- 13
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cell death & disease
- Publication Type :
- Academic Journal
- Accession number :
- 35075115
- Full Text :
- https://doi.org/10.1038/s41419-022-04525-1