Evidence map›Paper›PMID 30413194›Full record

ArticleBMC urology2018

Epidermal growth factor expression as a predictor of chemotherapeutic resistance in muscle-invasive bladder cancer.

Ahmed M Mansour, Mona Abdelrahim, Mahmoud Laymon, Mamdouh Elsherbeeny, Mohammed Sultan, Ahmed Shokeir, Ahmed Mosbah, Hassan Abol-Enein, Amira Awadalla, Eunho Cho and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC urology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  9. International journal of pharmaceutics: X · 2022
    Article
  10. Review
  11. Role of tyrosine kinases in bladder cancer progression: an overview.Cell communication and signaling : CCS · 2020
    Review
  12. 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

14 authors at 4 institutions in 2 countries.

Ahmed M MansourUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Mona AbdelrahimUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Mahmoud LaymonUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Mamdouh ElsherbeenyUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Mohammed SultanUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Ahmed ShokeirUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Ahmed MosbahUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Hassan Abol-EneinUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Amira AwadallaUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Eunho ChoUniversity of California Los Angeles, Los Angeles, CA, USA.
Vikram SairamUniversity of California Los Angeles, Los Angeles, CA, USA.
Taeeun D ParkUniversity of California, Berkerly, CA, USA.
Muhammad ShahidDepartments of Surgery and Biomedical Sciences, Samuel Oschin Comprehensive Cancer Institute, Cedars Sinai Medical Center, 8700 Beverly Blvd, Los Angeles, CA, 90048, USA.
Jayoung KimUniversity of California Los Angeles, Los Angeles, CA, USA. Jayoung.kim@csmc.edu.
Mansoura University · EGCedars-Sinai Medical Center · USUniversity of California, Los Angeles · USThe University of Texas Health Science Center at San Antonio · US

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
West Coast Central Comprehensive Metabolomics Resource Core (WC3MRC)U24DK097154 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI FIEHN, OLIVER · 2012 to 2017
$9.9M
Microbiome and Proteome As Predictive Biomarkers of UCPPSU01DK103260 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI ANGER, JENNIFER TASH, FREEMAN, MICHAEL R · 2014 to 2018
$1.2M
Urinary Metabolites in IC PBS DiagnosisR01DK100974 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI ANGER, JENNIFER TASH, KIM, JAYOUNG · 2013 to 2013
$416k
ACL HHS U01DP006079Centers for Disease Controls and Prevention 1U01DP006079NCATS NIH HHS UL1 TR000124NCCDPHP CDC HHS U01 DP006079NIDDK NIH HHS R01 DK100974NIDDK NIH HHS U01 DK103260NIDDK NIH HHS U24 DK097154NIH HHS 1R01DK100974NIH HHS 1U01DK103260U.S. Department of Defense W81XWH-15-1-0415
6 · The paper itself

Abstract

backgroundEpidermal growth factor receptor (EGFR) overexpression is believed to be associated with bladder cancer (BC) progression and poor clinical outcomes. In vivo studies have linked EGFR subcellular trafficking and chemo-resistance to cisplatin-based chemotherapies. This has not been studied in the clinical adjuvant setting. We aimed to investigate the prognostic significance of EGFR expression in patients receiving cisplatin-based adjuvant chemotherapy following radical cystectomy for advanced BC.

methodsThe database from the Urology and Nephrology Center at Mansoura University was reviewed. BC patients who were treated with radical cystectomy and adjuvant chemotherapy for adverse pathological features or node positive disease were identified. Patients who underwent palliative cystectomy, had histological diagnoses other than pure urothelial carcinoma, or received adjuvant radiotherapy were excluded from the study. Immunohistochemical staining for EGFR expression was performed on archived bladder specimens. The following in vitro functional analyses were performed to study the relationship of EGFR expression and chemoresponse.

resultsThe study included 58 patients, among which the mean age was 57 years old. Majority of patients had node positive disease (n = 53, 91%). Mean follow up was 26.61 months. EGFR was overexpressed in 25 cystectomy specimens (43%). Kaplan-Meier analysis revealed that EGFR over-expression significantly correlated with disease recurrence (p = 0.021). Cox proportional hazard modeling identified EGFR overexpression as an independent predictor for disease recurrence (p = 0.04). Furthermore, in vitro experiments demonstrated that inhibition of EGFR may sensitize cellular responses to cisplatin.

conclusionsOur findings suggest that EGFR overexpression is associated with disease recurrence following adjuvant chemotherapy for advanced BC. This may aid in patient prognostication and selection prior to chemotherapeutic treatment for BC.

Indexed as

Gene Expression Regulation, NeoplasticCells, CulturedCell SurvivalCisplatinDrug Resistance, NeoplasmEpidermal Growth FactorErbB ReceptorsFemaleFollow-Up StudiesHumansMaleMiddle AgedMuscle NeoplasmsNeoplasm InvasivenessPredictive Value of TestsUrinary Bladder NeoplasmsCisplatinEGFR protein, humanEpidermal Growth FactorErbB ReceptorsAdjuvant chemotherapyBladder cancerEGFRSurvival

Identifiers

PMID30413194
PMCPMC6234794
OpenAlexW2900312251

What OpenQuestion holds

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LicenceCC BY
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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.