Evidence map›Paper›PMID 33194740›Full record

ArticleFrontiers in oncology2020

Magnetic Resonance Molecular Imaging of Extradomain B Fibronectin Improves Imaging of Pancreatic Cancer Tumor Xenografts.

Peter Qiao, Nadia R Ayat, Amita Vaidya, Songqi Gao, Wenyu Sun, Samuel Chou, Zheng Han, Hannah Gilmore, Jordan M Winter, Zheng-Rong Lu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Peter QiaoDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Nadia R AyatDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Amita VaidyaDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Songqi GaoDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Wenyu SunDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Samuel ChouDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Zheng HanDepartment of Radiology and Radiological Science, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, MD, United States.
Hannah GilmoreDepartment of Pathology, University Hospitals Cleveland Medical Center, Cleveland, OH, United States.
Jordan M WinterCase Comprehensive Cancer Center, Case Western Reserve School of Medicine, Case Western Reserve University, Cleveland, OH, United States.
Zheng-Rong LuDepartment of Biomedical Engineering, Case School of Engineering, Case Western Reserve University, Cleveland, OH, United States.
Case Western Reserve University · USJohns Hopkins University · USUniversity Hospitals of Cleveland · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
NRSA Training CoreTL1TR002549 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI HARDING, CLIFFORD V · 2018 to 2022
$2.9M
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
NCATS NIH HHS TL1 TR002549NCI NIH HHS R01 CA211762NCI NIH HHS R44 CA199826NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

The survival of pancreatic cancer patients can be greatly improved if their disease is detected at an early, potentially curable stage. Magnetic resonance molecular imaging (MRMI) of oncoproteins is a promising strategy for accurate, early detection of the disease. Here, we test the hypothesis that MRMI of extradomain-B fibronectin (EDB-FN), an abundant oncoprotein in the tumor extracellular matrix, can overcome the stromal barriers of pancreatic cancer to facilitate effective molecular imaging and detection of small tumors. Specimens of normal, premalignant, and malignant human pancreatic tissues were stained with a peptide-fluorophore conjugate (ZD2-Cy5.5) to assess EDB-FN binding and expression. MRMI with ZD2-N3-Gd(HP-DO3A) (MT218) specific to EDB-FN and MRI with Gd(HP-DO3A) were performed in three murine models bearing human pancreatic cancer xenografts, including a Capan-1 flank model, a BxPC3-GFP-Luc and a PANC-1-GFP-Luc intrapancreatic xenograft model. Tumor enhancement of the contrast agents was analyzed and compared. Staining of human tissue samples with ZD2-Cy5.5 revealed high EDB-FN expression in pancreatic tumors, moderate expression in premalignant tissue, and little expression in normal tissue. MRMI with MT218 generated robust intratumoral contrast, clearly detected and delineated small tumors (smallest average size: 6.1 mm

Indexed as

extradomain B fibronectinmolecular imagingMRIpancreatic cancertumor microenvironment

Identifiers

PMID33194740
PMCPMC7661967
OpenAlexW3096159917

What OpenQuestion holds

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LicenceCC BY
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.