Evidence map›Paper›PMID 41778247›Full record

ArticleCancer diagnosis & prognosis

Immunohistochemical Expression of Endoplasmic Reticulum Stress Markers and their Association With Clinicopathological Characteristics and Survival Outcomes in Endometrial Cancer.

Stefanos Flindris, Chrysoula Margioula-Siarkou, Chrysoula Gouta, Konstantinos Christopoulos, Georgia Margioula-Siarkou, Emmanouela-Aliki Almperi, Aristarchos Almperis, Alexandros Traianos, Michail Kalinderis, Eleni Sakellariou and 9 more

Abstract read
In one paragraph

Article in Cancer diagnosis & prognosis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Stefanos Flindris2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Chrysoula Margioula-Siarkou *2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Chrysoula Gouta *Department of Pathology, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Konstantinos ChristopoulosDepartment of Hygiene and Epidemiology, University of Ioannina, School of Medicine, Ioannina, Greece.
Georgia Margioula-Siarkou2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Emmanouela-Aliki Almperi2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Aristarchos Almperis2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Alexandros Traianos2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Michail Kalinderis2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Eleni SakellariouDepartment of Pathology, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Konstantinos FlindrisDepartment of Ophthalmology, General Hospital of Ioannina "G. Hatzikosta", Ioannina, Greece.
Charalampos Karachalios2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Effrosyni StyliaraDepartment of Radiology, University Hospital of Ioannina, University of Ioannina, Ioannina, Greece.
Stamatia AngelidouDepartment of Pathology, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Konstantinos Pantazis2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Iordanis NavrozoglouDepartment of Obstetrics and Gynecology, University Hospital of Ioannina, University of Ioannina, School of Medicine, Ioannina, Greece.
Konstantinos Dinas2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.
Georgios Markozannes *Department of Hygiene and Epidemiology, University of Ioannina, School of Medicine, Ioannina, Greece.
Stamatios Petousis *2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, School of Medicine, General Hospital of Thessaloniki "Ippokratio", Thessaloniki, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aim: This study aimed to examine the immunohistochemical expression of Inositol-Requiring Enzyme 1 Alpha (IRE1) and Protein Kinase R-like ER Kinase (PERK) immunoreactivity scores (IRS) as emerging biomarkers on key clinicopathologic features and survival outcomes in endometrial cancer (EC). Patients and Methods: Immunoreactive scores (IRS) for IRE1 and PERK were assessed in tumor samples from 73 EC survivors and compared with 20 benign endometrial controls. Associations between IRS values and clinicopathological variables were analyzed. Overall survival (OS) and disease-free survival (DFS) were evaluated using univariable and multivariable Cox proportional hazards models adjusted for age, FIGO stage, and tumor grade. Results: IRE1-IRS and PERK-IRS were significantly higher in EC survivors compared to controls ( Conclusion: IRE1 and PERK expression is up-regulated in endometrial cancer and correlates with selected clinicopathological features, particularly those linked to aggressive disease. However, neither marker demonstrated independent prognostic value for survival outcomes. Further studies are warranted to clarify the role of ER stress pathways in EC biology and their potential implications for risk stratification and targeted therapy.

Indexed as

Endometrial cancerER stressIRE1PERKsurvivalUPR

Identifiers

PMID41778247
PMCPMC12951383

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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.