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Upregulation of the lncRNA SRLR in polycystic ovary syndrome regulates cell apoptosis and IL-6 expression.
- Source :
-
Cell biochemistry and function [Cell Biochem Funct] 2020 Oct; Vol. 38 (7), pp. 880-885. Date of Electronic Publication: 2020 Jan 30. - Publication Year :
- 2020
-
Abstract
- Increased levels of interleukin-6 (IL-6) contribute to the development of polycystic ovary syndrome (PCOS); in renal cell carcinoma, the long non-coding RNA (lncRNA) SRLR upregulates IL-6. In this study, we demonstrated that the levels of the lncRNA SRLR were upregulated in PCOS patients with high expression of plasma IL-6 compared with heathy females. The levels of the lncRNA SRLR in the plasma had a positive correlation with expression of IL-6 in patients with PCOS but not in healthy females. Upregulation of the lncRNA SRLR in plasma could distinguish PCOS patients from healthy females. Overexpression of the lncRNA SRLR led to upregulation of IL-6 and promoted apoptosis of human granulosa-like tumour cells (KGN). Therefore, the lncRNA SRLR participated in PCOS by regulating cell apoptosis and IL-6 expression. SIGNIFICANCE OF THE STUDY: The lncRNA SRLR mediates its effects on apoptosis and IL-6 expression in PCOS and could be used to distinguish PCOS patients from healthy controls. Plasma circulating levels of the lncRNA SRLR may be a potential target for the treatment of PCOS.<br /> (© 2020 The Authors. Cell Biochemistry and Function published by John Wiley & Sons Ltd.)
- Subjects :
- Adult
Area Under Curve
Case-Control Studies
Cells, Cultured
Female
Granulosa Cells cytology
Granulosa Cells metabolism
Humans
Interleukin-6 metabolism
Oxazolidinones pharmacology
Polycystic Ovary Syndrome genetics
RNA Interference
RNA, Long Noncoding antagonists & inhibitors
RNA, Long Noncoding blood
RNA, Long Noncoding genetics
RNA, Small Interfering metabolism
ROC Curve
Up-Regulation
Young Adult
Apoptosis drug effects
Interleukin-6 blood
Polycystic Ovary Syndrome diagnosis
RNA, Long Noncoding metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1099-0844
- Volume :
- 38
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Cell biochemistry and function
- Publication Type :
- Academic Journal
- Accession number :
- 31999854
- Full Text :
- https://doi.org/10.1002/cbf.3507