Article in Molecular cancer research : MCR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
0numbers the graph read from it
0cells of the map it votes in
4citing 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.
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
18 authors.
Joseph E IppolitoDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-1913-5573
Jordan P HartigDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.ORCID 0009-0000-2569-3585
Kaitlyn BejarDepartment of Cell Systems and Anatomy, University of Texas Health at San Antonio, San Antonio, Texas.ORCID 0000-0002-3911-9290
Hani NakhoulDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0002-8045-2175
Jennifer K SehnDepartment of Pathology, Saint Louis University School of Medicine, St. Louis, Missouri.ORCID 0000-0002-7858-7425
Cody WeimholtDepartment of Pathology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-2926-343X
Grace GrimsleyDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.ORCID 0009-0001-0639-3672
Elena NunezDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-4911-8176
Nikolaos A TrikalinosSiteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0001-8611-2182
Deyali ChatterjeeDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0002-3322-1163
Anand S MehtaDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0002-9846-9389
Peggi M AngelDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0002-4436-555X
Dean A TroyerDepartment of Microbiology, Eastern Virginia Medical School, San Antonio, Texas.ORCID 0000-0002-0337-5890
Robin J LeachDepartment of Cell Systems and Anatomy, University of Texas Health at San Antonio, San Antonio, Texas.ORCID 0000-0002-3201-5579
Eva CoreyDepartment of Urology, University of Washington, Seattle, Washington.ORCID 0000-0002-9244-3807
Jennifer D WuDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.ORCID 0000-0002-8925-268X
Richard R DrakeDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0002-6285-6440
Funding
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI EVA COREY · 2013 to 2026
$25.0M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Tumor immune and glycan biomarkers for progressive prostate cancerR01CA212409 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., DRAKE, RICHARD R. · 2018 to 2022
$2.7M
Diffusion Histology Imaging: A Clinical Tool to Non-Invasively Diagnose and Manage Prostate CancerR01CA258690 · NCI · WASHINGTON UNIVERSITY · PI Joseph Edward Ippolito, Michael Hiroshi Johnson · 2022 to 2026
$2.7M
Identifying lethal prostate cancer at diagnosis with advanced proteoglycomic, radiomic, and genomic approachesR01CA282022 · NCI · WASHINGTON UNIVERSITY · PI Joseph Edward Ippolito, Eric H Kim · 2023 to 2026
$2.4M
Training OPportunities in Translational Imaging Education and Research (TOP-TIER)T32EB021955 · NIBIB · WASHINGTON UNIVERSITY · PI Hongyu An, Joseph Edward Ippolito · 2017 to 2026
$2.4M
CTSA Predoctoral T32 at The University of Texas Health Science Center at San AntonioT32TR004545 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Yong-Hee Patricia Chun, Christopher R. Frei · 2023 to 2026
$1.1M
Identifying gut bacterial molecules and mechanisms that promote an anti-tumor response to immunotherapyK22CA258960 · NCI · HARVARD MEDICAL SCHOOL · PI GAZZANIGA, FRANCESCA SMYLIE · 2022 to 2024
$559k
Alvin J. Siteman Cancer Center (SCC)American Cancer Society (ACS) TLC-23-1180705-01-TLCFoundation for Barnes-Jewish Hospital (FBJH)National Cancer Institute (NCI) P50CA97186National Cancer Institute (NCI) R01CA282022NCATS NIH HHS T32 TR004545NCI NIH HHS K22 CA258960NCI NIH HHS P01 CA163227NCI NIH HHS P50 CA097186NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA212409NCI NIH HHS R01 CA258690NCI NIH HHS R01 CA282022NIBIB NIH HHS T32 EB021955Prostate Cancer Foundation (PCF)U.S. Department of Defense (DOD) W81XWH-19-1-0795
6 · The paper itself
Abstract
Prostate cancer is a heterogeneous disease with a spectrum of pathology and outcomes ranging from indolent to lethal. Although there have been recent advancements in prognostic tissue biomarkers, limitations still exist. We leveraged matrix-assisted laser desorption/ionization imaging of formalin-fixed, paraffin embedded prostate cancer specimens to determine if N-linked glycans expressed in the extracellular matrix of lethal neuroendocrine prostate cancer were also expressed in conventional prostate adenocarcinomas that were associated with poor outcomes. We found that N-glycan fucosylation was abundant in neuroendocrine prostate cancer as well as adenocarcinomas at the time of prostatectomy that eventually developed recurrent metastatic disease. Analysis of patient-derived xenografts revealed that this fucosylation signature was enriched differently across metastatic disease organ sites, with the highest abundance in liver metastases. These data suggest that N-linked fucosylated glycans could be an early tissue biomarker for poor prostate cancer outcomes. Implications: These studies identify that hyper-fucosylated N-linked glycans are enriched in neuroendocrine prostate cancer and conventional prostate adenocarcinomas that progress to metastatic disease, thus advancing biomarker discovery and providing insights into mechanisms underlying metastatic disease.
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.
N-Linked Fucosylated Glycans Are Biomarkers for Prostate Cancer with a Neuroendocrine and Metastatic Phenotype. · full record | OpenQuestion