4.7 Article

Identification of Novel Biomarkers and Candidate Drug in Ovarian Cancer

期刊

JOURNAL OF PERSONALIZED MEDICINE
卷 11, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/jpm11040316

关键词

ovarian cancer; bioinformatics; CREB1; drug perturbation

资金

  1. Ministry of Science Technology [MOST-109-2314-B-075B-014-MY2, MOST 109-2314-B-075B-002]
  2. Kaohsiung Veterans General Hospital [VGHKS109-103, 109-105, 109-106, 109-D07, 110-088, 110-143, 110-090, 110-D06]

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The study reveals higher expression of CREB1 gene in ovarian cancer tissue compared to normal tissue, and indicates that high expression of CREB1 gene may lead to poor prognosis. Targeting CREB1 could be a potential tool for the diagnosis and treatment of ovarian cancer.
This paper investigates the expression of the CREB1 gene in ovarian cancer (OV) by deeply excavating the gene information in the multiple databases and the mechanism thereof. In short, we found that the expression of the CREB1 gene in ovarian cancer tissue was significantly higher than that of normal ovarian tissue. Kaplan-Meier survival analysis showed that the overall survival was significantly shorter in patients with high expression of the CREB1 gene than those in patients with low expression of the CREB1 gene, and the prognosis of patients with low expression of the CREB1 gene was better. The CREB1 gene may play a role in the occurrence and development of ovarian cancer by regulating the process of protein. Based on differentially expressed genes, 20 small-molecule drugs that potentially target CREB1 with abnormal expression in OV were obtained from the CMap database. Among these compounds, we found that naloxone has the greatest therapeutic value for OV. The high expression of the CREB1 gene may be an indicator of poor prognosis in ovarian cancer patients. Targeting CREB1 may be a potential tool for the diagnosis and treatment of OV.

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