4.6 Article

Disregulations of PURPL and MiR-338-3p Could Serve As Prognosis Biomarkers for Epithelial Ovarian Cancer

Journal

JOURNAL OF CANCER
Volume 12, Issue 18, Pages 5674-5680

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/jca.61327

Keywords

biomedical database; epithelial ovarian cancer; PURPL; miR-338-3p; prognosis

Categories

Funding

  1. Scientific and technological projects of Henan Province [202102310392]
  2. Youth Innovation Fund Project of the First Affiliated Hospital of Zhengzhou University [201418]

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The study explored the expressions of lncRNA PURPL in different ovarian tissues and evaluated its significance in EOC. Results showed that upregulation of PURPL and downregulation of miR-338-3p were related to poor prognosis in ovarian cancer. High levels of PURPL and low levels of miR-338-3p expressions were associated with worse RFS and OS in patients.
Objective: The present study aimed to explore the expressions of long noncoding RNA (lncRNA) p53 upregulated regulator of p53 levels (PURPL) in different ovarian tissues, and to evaluate the significance of disregulations of PURPL and microRNA-338-3p (miR-338- 3p) in epithelial ovarian cancer (EOC). Methods: The expressions of PURPL in ovarian cancer, the relations between PURPL and the prognosis of ovarian cancer, and the relation between PURPL and miR-338-3p were queried in multiple biomedical databases. Real-time PCR was performed to detect the expressions of PURPL in different ovarian tissues. Logistic regression analysis was used to analyze the risk factors of recurrence and death. Kaplan-Meier analysis was implemented to evaluate the relations between PURPL and miR-338-3p expressions and the survival of ovarian cancer. Results: PURPL could target miR-338-3p, PURPL were upregulated in ovarian cancer tissues, upregulation of PURPL in ovarian cancer was negatively related with the recurrence free survival (RFS) and overall survival (OS), which were indicated by biomedical databases query. Our data showed upregulations of PURPL were noted in ovarian cancer tissues. Higher expressions of PURPL were associated with more advanced FIGO stage and developed lymph node metastasis in epithelial ovarian cancer. Upregulation of PURPL was related with the recurrence ( P=0.002, OR=21.482, 95%CI: 3.457 similar to 94.251) and death (P=0.004, OR=35.643, 95%CI: 2.453 similar to 84.359) of ovarian cancer patient. PURPL expressions were negatively correlated to miR-338-3p expressions in different ovarian tissues (r = -0.968, P<0.0001). Poor RFS (chi(2)=19.410, P=0.0002) and OS (chi(2)=17.600, P=0.0005) were found in patients with high level PURPL and low level miR-338-3p expressions. Conclusions: Upregulation of PURPL and downregulation of miR-338-3p were related with the poor RFS and OS of ovarian cancer, which indicated disregulations of PURPL and miR-338-3p could serve as prognosis biomarkers for epithelial ovarian cancer.

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