Evidence map›Paper›PMID 37774079›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

Clinicopathologic Impact of NANOG, ZEB1, and EpCAM Biomarkers on Prognosis of Serous Ovarian Carcinoma.

Hanaa M Ibrahim, Aziza E Abdelrahman, Eman Elsebai, Shimaa A Gharieb, Moamna M Fahmy, Mohamed S H Ramadan, Mohamed A Wasfy, Asmaa Abdullatif

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

8 authors at 1 institution in 1 country.

Hanaa M IbrahimDepartment of Pathology, Faculty of Medicine, Zagazig University, Egypt.
Aziza E AbdelrahmanDepartment of Pathology, Faculty of Medicine, Zagazig University, Egypt.
Eman ElsebaiDepartment of Clinical Oncology, Faculty of Medicine, Zagazig University, Egypt.
Shimaa A GhariebDepartment of Clinical Oncology, Faculty of Medicine, Zagazig University, Egypt.
Moamna M FahmyDepartment of Clinical Oncology, Faculty of Medicine, Zagazig University, Egypt.
Mohamed S H RamadanDepartment of Gynecology and Obstetrics, Faculty of Medicine, Zagazig University, Egypt.
Mohamed A WasfyDepartment of Gynecology and Obstetrics, Faculty of Medicine, Zagazig University, Egypt.
Asmaa AbdullatifDepartment of Pathology, Faculty of Medicine, Zagazig University, Egypt.
Zagazig University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSerous ovarian carcinoma (SOC) is a biologically heterogeneous with different genomic and molecular profiles, beside clinical response to the chemotherapy with subsequent in obstacles in starting unified, acceptable treatments and so we assess immunoexpression of Nanog, ZEB1, and EpCAM in SOC.

methodsIn this study, the immunoexpression of Nanog, ZEB1, and EpCAM was studied in 60 cases of SOC. Overall survival (OS), disease-free survival (DFS) data and response to chemotherapy were  analyzed.

resultsNANOG was immunostained in 65% of the cases with a significant association with tumor grade, lymph node metastasis, and FIGO stage (p < 0.001 for each). ZEB1 showed moderate- high expression in 58.3% of the cases with significant up-regulation of ZEB1 expression with SOC grade, nodal metastasis, and SOC FIGO stage (p<0.001). EpCAM revealed high expression in 60% of the cases with significant association with higher grade, nodal metastasis, and advanced stage (p < 0.001 for each). Up-regulation of Nanog was significantly associated with response to chemotherapy, relapse, shorter OS and DFS (p < 0.001 for each). ZEB1 overexpression exhibited a significant association with response to chemotherapy (p= 0.012), relapse, shorter OS and DFS (p<0.001 for each). Moreover, the high EpCAM had a significant association with response to chemotherapy (p= 0.043), relapse (p < 0.001) shorter OS (p=0.006) and DFS (p< 0.001).

conclusionsUp-regulation of Nanog and ZEB-1 and EpCAM perhaps promote an aggressive SOC with a high risk of relapse and unfavorable response to standard chemotherapy regimen.

Indexed as

Cystadenocarcinoma, SerousOvarian NeoplasmsBiomarkers, TumorCarcinoma, Ovarian EpithelialEpithelial Cell Adhesion MoleculeFemaleHumansNanog Homeobox ProteinNeoplasm Recurrence, LocalNeoplasm StagingPrognosisZinc Finger E-box-Binding Homeobox 1Biomarkers, TumorEPCAM protein, humanEpithelial Cell Adhesion MoleculeNanog Homeobox ProteinNANOG protein, humanZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1EpCAMNanogPrognosisSerous ovarian carcinomaZEB-1

Identifiers

PMID37774079
PMCPMC10762767
OpenAlexW4387164478

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.