Evidence map›Paper›PMID 31856408›Full record

ArticleCancer medicine2020

Bioinformatic profiling identifies a platinum-resistant-related risk signature for ovarian cancer.

Ce Wu, Linxiu He, Qian Wei, Qian Li, Longyang Jiang, Lan Zhao, Chunyan Wang, Jianping Li, Minjie Wei

Abstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ce WuDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.ORCID 0000-0002-3791-5912
Linxiu HeDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.
Qian WeiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.
Qian LiLiaoning Cancer Hospital and Institute, Cancer Hospital of China Medical University, Shenyang City, China.
Longyang JiangDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.
Lan ZhaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.
Chunyan WangLiaoning Cancer Hospital and Institute, Cancer Hospital of China Medical University, Shenyang City, China.
Jianping LiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.
Minjie WeiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, China.ORCID 0000-0002-0404-7098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most high-grade serous ovarian cancer (HGSOC) patients develop resistance to platinum-based chemotherapy and recur. Many biomarkers related to the survival and prognosis of drug-resistant patients have been delved by mining databases; however, the prediction effect of single-gene biomarker is not specific and sensitive enough. The present study aimed to develop a novel prognostic gene signature of platinum-based resistance for patients with HGSOC. The gene expression profiles were obtained from Gene Expression Omnibus and The Cancer Genome Atlas database. A total of 269 differentially expressed genes (DEGs) associated with platinum resistance were identified (P < .05, fold change >1.5). Functional analysis revealed that these DEGs were mainly involved in apoptosis process, PI3K-Akt pathway. Furthermore, we established a set of seven-gene signature that was significantly associated with overall survival (OS) in the test series. Compared with the low-risk score group, patients with a high-risk score suffered poorer OS (P < .001). The area under the curve (AUC) was found to be 0.710, which means the risk score had a certain accuracy on predicting OS in HGSOC (AUC > 0.7). Surprisingly, the risk score was identified as an independent prognostic indicator for HGSOC (P < .001). Subgroup analyses suggested that the risk score had a greater prognostic value for patients with grade 3-4, stage III-IV, venous invasion and objective response. In conclusion, we developed a seven-gene signature relating to platinum resistance, which can predict survival for HGSOC and provide novel insights into understanding of platinum resistance mechanisms and identification of HGSOC patients with poor prognosis.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorComputational BiologyCystadenocarcinoma, SerousDatasets as TopicDrug Resistance, NeoplasmFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansModels, GeneticOligonucleotide Array Sequence AnalysisOrganoplatinum CompoundsOvarian NeoplasmsPhosphatidylinositol 3-KinasesPrognosisBiomarkers, TumorOrganoplatinum CompoundsPhosphatidylinositol 3-KinasesRNA, Messengerbioinformaticshigh-grade serous ovarian cancerplatinum resistanceprognosis

Identifiers

PMID31856408
PMCPMC6997076

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.