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2017 ; 8
(14
): 23650-23663
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Identification of long non-coding RNAs GAS5, linc0597 and lnc-DC in plasma as
novel biomarkers for systemic lupus erythematosus
#MMPMID28423570
Wu GC
; Li J
; Leng RX
; Li XP
; Li XM
; Wang DG
; Pan HF
; Ye DQ
Oncotarget
2017[Apr]; 8
(14
): 23650-23663
PMID28423570
show ga
Despite increasing evidence that long non-coding RNAs (lncRNAs) widely take part
in human diseases, the role of lncRNAs in systemic lupus erythematosus (SLE) is
largely unknown. In this study, we performed a two-stage study to explore the
plasma levels of five lncRNAs (GAS5, linc0949, linc0597, HOTAIRM1 and lnc-DC) and
their potential as SLE biomarkers. Compared with healthy controls, plasma levels
of GAS5 and lnc-DC were significantly decreased (P < 0.001 and P = 0.002,
respectively) while linc0597 were overexpressed in SLE patients (P < 0.001). When
SLE patients were divided into SLE without nephritis and lupus nephritis (LN),
the levels of lnc-DC were significantly higher in LN compared with SLE without
nephritis (P = 0.018), but no significant difference in levels of GAS5 and
linc0597 were found between LN and SLE without nephritis; plasma linc0949 level
showed no significant difference in all comparisons. Further evaluation on
potential biomarkers showed that GAS5, linc0597 and lnc-DC may specifically
identify patients with SLE, the combination of GAS5 and linc0597 provided better
diagnostic accuracy; lnc-DC may discriminate LN from SLE without nephritis. In
summary, GAS5, linc0597 and lnc-DC in plasma could be potential biomarkers for
SLE.