Evidence map›Paper›PMID 30165429›Full record

Trial reportCarcinogenesis2018

Expression of IGF/insulin receptor in prostate cancer tissue and progression to lethal disease.

Thomas U Ahearn, Sam Peisch, Andreas Pettersson, Ericka M Ebot, Cindy Ke Zhou, Rebecca E Graff, Jennifer A Sinnott, Ladan Fazli, Gregory L Judson, Tarek A Bismar and 14 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Carcinogenesis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Increased ErbB2 Signaling Is an Early Adaptation to Androgen Signaling Inhibition and Persists in Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  5. International journal of molecular sciences · 2025
    Article
  6. Review
  7. Article
  8. Insulin-related traits and prostate cancer: A Mendelian randomization study.Computational and structural biotechnology journal · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Postdiagnostic Inflammatory, Hyperinsulinemic, and Insulin-Resistant Diets and Lifestyles and the Risk of Prostate Cancer Progression and Mortality.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  18. Article
  19. Article
  20. 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

24 authors at 9 institutions in 4 countries.

Thomas U AhearnDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Sam PeischDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Andreas PetterssonDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Ericka M EbotDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Cindy Ke ZhouDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Rebecca E GraffDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Jennifer A SinnottDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Ladan FazliVancouver Prostate Center, Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Gregory L JudsonDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Tarek A BismarDepartment of Pathology and Laboratory Medicine, University of Calgary and Calgary Laboratory Services, Calgary, Alberta, Canada.
Jennifer R RiderDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Travis GerkeDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
June M ChanDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, USA.
Michelangelo FiorentinoPathology Unit, Addarii Institute, S. Orsola-Malpighi Hospital, Bologna, Italy.
Richard FlavinDepartment of Histopathology Research, Trinity College, Dublin, Ireland.
Howard D SessoDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Stephen FinnDepartment of Histopathology Research, Trinity College, Dublin, Ireland.
Edward L GiovannucciDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Martin GleaveVancouver Prostate Center, Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Massimo LodaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Zhe LiDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Michael PollakCancer Prevention Research Unit, Departments of Medicine and Oncology, Lady Davis Research Institute of the Jewish General Hospital and McGill University, Montreal, Quebec, Canada.
Lorelei A MucciDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Transdisciplinary Prostate Cancer Partnership (ToPCaP)
Harvard University · USBrigham and Women's Hospital · USTrinity College Dublin · IEUniversity of British Columbia · CADana-Farber Cancer Institute · USKarolinska Institutet · SEMcGill University · CAUniversity of Calgary · CAUniversity of California, San Francisco · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI Irene M. Ghobrial · 1985 to 2026
$330.6M
Tumor and Circulating Markers as Links Between Obesity and Lethal Prostate CanceP50CA090381 · NCI · DANA-FARBER CANCER INSTITUTE · PI KANTOFF, PHILIP W · 2002 to 2017
$36.2M
Training Program in Cancer EpidemiologyT32CA009001 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI A. Heather Eliassen, Meir Stampfer · 1985 to 2026
$17.3M
Cancer Epidemiology Cohort in Male Health ProfessionalsU01CA167552 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Lorelei Mucci, Walter C. Willett · 2017 to 2026
$17.0M
Cancer Epidemiology Cohort in Male Health ProfessionalsUM1CA167552 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI WILLETT, WALTER C. · 2012 to 2016
$11.5M
Training in Molecular& Genetic Epidemiology of CancerR25CA112355 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTE, JOHN S. · 2005 to 2018
$6.5M
Growth Factors and Lethal Prostate Cancer SignatureR01CA141298 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI STAMPFER, MEIR · 2010 to 2013
$2.2M
Sex-Hormones and the TMPRSS2: ERG Fusion in Prostate Cancer ProgressionR01CA136578 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI MUCCI, LORELEI · 2009 to 2013
$1.7M
NCI NIH HHS P30 CA006516NCI NIH HHS P50 CA090381NCI NIH HHS R01 CA136578NCI NIH HHS R01 CA141298NCI NIH HHS R25 CA112355NCI NIH HHS T32 CA009001NCI NIH HHS U01 CA167552NCI NIH HHS UM1 CA167552
6 · The paper itself

Abstract

Circulating insulin-like growth factor-1 (IGF-1) is consistently associated with prostate cancer risk. IGF-1 binds to IGF-1 receptor (IGF1R) and insulin receptor (IR), activating cancer hallmark pathways. Experimental evidence suggests that TMPRSS2:ERG may interact with IGF/insulin signaling to influence progression. We investigated IGF1R and IR expression and its association with lethal prostate cancer among 769 men. Protein expression of IGF1R, IR and ERG (i.e. a surrogate of ERG fusion genes) were assayed by immunohistochemistry. Cox models estimated hazard ratios (HR) and 95% confidence intervals (CI) adjusted for clinical characteristics. Among patients, 29% had strong tumor IGF1R expression and 10% had strong IR expression. During a mean follow-up of 13.2 years through 2012, 80 men (11%) developed lethal disease. Tumors with strong IGF1R or IR expression showed increased cell proliferation, decreased apoptosis and a higher prevalence of ERG. In multivariable models, strong IGF1R was associated with a borderline increased risk of lethal prostate cancer (HR 1.7; 95% CI 0.9-3.1). The association appeared greater in ERG-positive tumors (HR 2.8; 95% CI 0.9-8.4) than in ERG-negative tumors (HR 1.3; 95% CI 0.6-3.0, p-heterogeneity 0.08). There was no association between IR and lethal prostate cancer (HR 0.8; 95% CI 0.4-1.9). These results suggest that tumor IGF1R expression may play a role in prostate cancer progression to a lethal phenotype and that ERG-positive tumors may be more sensitive to IGF signaling. These data may improve our understanding of IGF signaling in prostate cancer and suggest therapeutic options for disease subtypes.

Indexed as

AgedApoptosisBiomarkers, TumorCell ProliferationDisease ProgressionGene Expression Regulation, NeoplasticHumansInsulinInsulin-Like Growth Factor IMaleOncogene Proteins, FusionProstatic NeoplasmsReceptor, IGF Type 1Receptor, InsulinReceptors, SomatomedinSignal TransductionBiomarkers, TumorIGF1 protein, humanIGF1R protein, humanInsulinInsulin-Like Growth Factor IOncogene Proteins, FusionReceptor, IGF Type 1Receptor, InsulinReceptors, SomatomedinTranscriptional Regulator ERG

Identifiers

PMID30165429
PMCPMC6314328
OpenAlexW2888695891

What OpenQuestion holds

Textmetadata
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.