Key result
High LOXL1-AS1 levels linked to shorter overall survival and diagnose high-grade EOC with ~0.84 AUC.
Why the study?
The diagnostic and prognostic value of circulating LOXL1-AS1 in epithelial ovarian cancer patients was not well established.
Does circulating LOXL1-AS1 serve as a diagnostic and prognostic biomarker in patients with epithelial ovarian cancer?
Observational (n=228)
Does circulating LOXL1-AS1 serve as a diagnostic and prognostic biomarker in patients with epithelial ovarian cancer?
p-value: p=0.0006
Circulating LOXL1-AS1 may serve as a novel diagnostic biomarker and independent prognostic indicator for poor clinical outcomes in epithelial ovarian cancer.
May support LOXL1-AS1 as EOC biomarker; leaves open incremental value pending prospective validation.
BACKGROUND: The present study aimed to examine the levels of circulating LOXL1-AS1 in epithelial ovarian cancer (EOC) patients and to analyze its diagnostic and prognostic value. METHODS: The levels of LOXL1-AS1 in 185 EOC patients and 43 healthy volunteers were evaluated by a quantitative reverse transcriptase-polymerase chain reaction. The potential of LOXL1-AS1 as a biomarker for EOC diagnosis was determined by receiver-operating characteristic (ROC) curve assays. The associations between clinicopathological parameters and LOXL1-AS1 expression were analyzed using a chi-squared test. The influence of LOXL1-AS1 on overall survival was analyzed by the use of Kaplan-Meier. A Cox proportional hazards assays were conducted for the determination of the prognostic value of LOXL1-AS1. RESULTS: The expression of LOXL1-AS1 was dramatically higher in EOC patients compared to healthy controls (p < 0.01). LOXL1-AS1 yielded an area under the ROC curve of 0.843 with 65.3% sensitivity and 68.2% specificity in discriminating high-grade EOC from healthy controls. It was also shown that LOXL1-AS1 expression was associated with advanced FIGO stage (p = 0.004) and positively distant metastasis (p = 0.013). Kaplan-Meier assays revealed that patients with high LOXL1-AS1 expression had a shorter overall survival than those with low expression (p = 0.0006). By performing multivariate assays, LOXL1-AS1 was confirmed to be an independent prognostic factor for predicting the prognosis of EOC patients. CONCLUSIONS: We provide evidence indicating that LOXL1-AS1 expression is correlated with a poor clinical outcome in EOC patients and may act as an independent prognostic indicator, as well as a new diagnostic biomarker.
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Liu et al. (2020) conducted an observational in Epithelial ovarian cancer (n=228). High LOXL1-AS1 expression vs. Low LOXL1-AS1 expression / Healthy controls was evaluated on Overall survival (p=0.0006). High LOXL1-AS1 expression was associated with shorter overall survival in epithelial ovarian cancer patients (P=0.0006) and discriminated high-grade EOC from healthy controls (AUC 0.843).
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