Evidence map›Paper›PMID 28201871›Full record

ArticleBioconjugate chemistry2017

Targeted Contrast Agent Specific to an Oncoprotein in Tumor Microenvironment with the Potential for Detection and Risk Stratification of Prostate Cancer with MRI.

Zheng Han, Yajuan Li, Sarah Roelle, Zhuxian Zhou, Yuchi Liu, Rob Sabatelle, Aidan DeSanto, Xin Yu, Hui Zhu, Cristina Magi-Galluzzi and 1 more

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  8. PET Imaging of Hepatocellular Carcinoma Using ZD2-(Journal of hepatocellular carcinoma · 2023
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  12. Review
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  17. Review
  18. Article
  19. Synthesis and assessment of ZD2-(American journal of nuclear medicine and molecular imaging · 2019
    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

11 authors at 4 institutions in 1 country.

Zheng HanCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Yajuan LiMolecular Theranostics, LLC , Beachwood, Ohio 44122, United States.
Sarah RoelleCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Zhuxian ZhouCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Yuchi LiuCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Rob SabatelleCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Aidan DeSantoCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Xin YuCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.
Hui Zhu
Cristina Magi-Galluzzi
Zheng-Rong LuCase Center for Biomolecular Engineering, Department of Biomedical Engineering, Case Western Reserve University , 10900 Euclid Avenue, Cleveland, Ohio 44106, United States.ORCID 0000-0001-8185-9519
Case Western Reserve University · USCase Comprehensive Cancer CenterCleveland Clinic · USMolecular Theranostics (United States) · US

Funding

Biodegradable Macromolecular Blood Pool Contrast AgentsR01EB000489 · NIBIB · UNIVERSITY OF UTAH · PI LU, ZHENG-RONG · 2003 to 2014
$3.3M
Targeted MRI contrast agents for differential diagnosis of prostate cancerR01CA211762 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI LU, ZHENG-RONG · 2017 to 2021
$2.1M
Commercialization of an MRI contrast agent for differential diagnosis of prostate cancer.R44CA199826 · NCI · MOLECULAR THERANOSTICS, LLC · PI LI, YAJUAN · 2017 to 2019
$2.1M
Monte Carlo Based Patient Radiation Dose from CTR01EB004898 · NIBIB · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCNITT-GRAY, MICHAEL F · 2005 to 2008
$1.5M
Commercialization of targeted MRI contrast agents for prostate cancer imaging.R43CA199826 · NCI · MOLECULAR THERANOSTICS, LLC · PI LI, YAJUAN · 2015 to 2015
$250k
NCI NIH HHS R01 CA211762NCI NIH HHS R43 CA199826NCI NIH HHS R44 CA199826NIBIB NIH HHS R01 EB000489NIBIB NIH HHS R01 EB004898
6 · The paper itself

Abstract

Accurate detection and risk stratification are paramount to the clinical management of prostate cancer. Current diagnostic methods, including prostate specific antigen (PSA) screening, are unable to differentiate high-risk tumors from low-risk tumors, resulting in overdiagnosis and overtreatment. A peptide targeted contrast agent, ZD2-Gd(HP-DO3A), specific to an oncoprotein in tumor microenvironment, EDB-FN, was synthesized for noninvasive detection and characterization of aggressive prostate cancer. EDB-FN, one of the subtypes of oncofetal fibronectin, is involved in tumor epithelial-to-mesenchymal transition (EMT), which is implicated in drug resistance and metastasis. The EDB-FN mRNA level in the metastatic PC3 cells was at least three times higher than that in non-metastatic LNCaP cells. In tumors, EDB-FN protein was highly expressed in PC3 tumor xenografts, but not in LNCaP tumors, as revealed by Western blot analysis. ZD2-Gd(HP-DO3A) produced over two times higher contrast-to-noise ratio in the PC3 tumors than in the LNCaP tumors in contrast-enhanced MRI during 30 min after injection. ZD2-Gd(HP-DO3A) possessed high chelate stability against transmetalation and minimal tissue accumulation. Our results demonstrate that molecular MRI of EDB-FN with ZD2-Gd(HP-DO3A) can potentially be used for noninvasive detection and risk stratification of human prostate cancer. Incorporation of this targeted contrast agent in the existing clinical contrast enhanced MRI procedures has the potential to improve diagnostic accuracy of prostate cancer.

Indexed as

Tumor MicroenvironmentCell Line, TumorContrast MediaHumansMagnetic Resonance ImagingMaleOncogene ProteinsProstatic NeoplasmsRisk AssessmentContrast MediaOncogene Proteins

Identifiers

PMID28201871
PMCPMC6075728
OpenAlexW2588684594

What OpenQuestion holds

Textmetadata
LicenceTDM
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.