Evidence map›Paper›PMID 30055028›Full record

ArticleJournal of cellular and molecular medicine2018

Variants in Notch signalling pathway genes, PSEN1 and MAML2, predict overall survival in Chinese patients with epithelial ovarian cancer.

Yuan Xu, Lei Cheng, Hongji Dai, Ruoxin Zhang, Mengyun Wang, Tingyan Shi, Menghong Sun, Xi Cheng, Qingyi Wei

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Effect ofFrontiers in genetics · 2022
    Article
  4. Article
  5. Identification of a Locus NearCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Correlation ofOncology letters · 2019
    Article
  10. 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 at 5 institutions in 2 countries.

Yuan XuCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Lei ChengCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Hongji DaiDepartment of Epidemiology and Biostatistics, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China.
Ruoxin ZhangCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Mengyun WangCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Tingyan ShiOvarian Cancer Program, Division of Gynecologic Oncology, Department of Gynecology and Obstetrics, Fudan University Zhongshan Hospital, Shanghai, China.
Menghong SunDepartment of Pathology, Tissue Bank, Fudan University Shanghai Cancer Center, Shanghai, China.
Xi ChengCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Qingyi WeiCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID 0000-0002-3845-9445
Shanghai Medical College of Fudan University · CNDuke University · USFudan University · CNFudan University Shanghai Cancer Center · CNTianjin Medical University Cancer Institute and Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To identify genetic variants in Notch signalling pathway genes that may predict survival of Han Chinese patients with epithelial ovarian cancer (EOC), we analysed a total of 1273 single nucleotide polymorphisms (SNPs) within 75 Notch genes in 480 patients from a published EOC genomewide association study (GWAS). We found that PSEN1 rs165934 and MAML2 rs76032516 were associated with overall survival (OS) of patients by multivariate Cox proportional hazards regression analysis. Specifically, the PSEN1 rs165934 AA genotype was associated with a poorer survival (adjusted hazards ratio [adjHR] = 1.41, 95% CI = 1.07-1.84, and P = .014), compared with the CC + CA genotype, while MAML2 rs76032516 AA + AC genotypes were associated with a poorer survival (adjHR = 1.58, 95% CI = 1.16-2.14, P = .004), compared with the CC genotype. The combined analysis of these two SNPs revealed that the death risk increased as the number of unfavourable genotypes increased in a dose-dependent manner (P

Indexed as

PrognosisAdultAgedAged, 80 and overCarcinoma, Ovarian EpithelialChinaDNA-Binding ProteinsDNA RepairFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansKaplan-Meier EstimateMiddle AgedDNA-Binding ProteinsMAML2 protein, humanNuclear ProteinsPresenilin-1PSEN1 protein, humanReceptors, NotchTrans-ActivatorsTranscription Factorsepithelial ovarian cancerMAML2Notch pathwayPSEN1single nucleotide polymorphisms

Identifiers

PMID30055028
PMCPMC6156353
OpenAlexW2884668920

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.