Evidence map›Paper›PMID 30228208›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

A PET Imaging Strategy for Interrogating Target Engagement and Oncogene Status in Pancreatic Cancer.

Kelly E Henry, Megan M Dacek, Thomas R Dilling, Jonathan D Caen, Ian L Fox, Michael J Evans, Jason S Lewis

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. 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
1.8field-weighted citation impact, top 14% 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, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Exploiting the MUC5AC Antigen for Noninvasive Identification of Pancreatic Cancer.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  8. Pancreatic Ductal Adenocarcinoma: The Dawn of the Era of Nuclear Medicine?International journal of molecular sciences · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
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

7 authors at 2 institutions in 1 country.

Kelly E HenryDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Megan M DacekProgram of Molecular Pharmacology and Chemistry, Memorial Sloan Kettering Cancer Center, New York, New York.
Thomas R DillingDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jonathan D CaenDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ian L FoxDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Michael J EvansDepartments of Radiology and Biomedical Imaging, and Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California.ORCID 0000-0003-4947-1316
Jason S LewisDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York. lewisj2@mskcc.org.ORCID 0000-0001-7065-4534
Memorial Sloan Kettering Cancer Center · USUniversity of California, San Francisco · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Annotating Oncogene Status in Prostate Cancer with Zr-89-transferrin PETR01CA176671 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI EVANS, MICHAEL JOHN, LEWIS, JASON S. · 2013 to 2017
$3.1M
Biomarkers for predicting response to Hsp90 therapyR01CA172546 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHIOSIS, GABRIELA, DUNPHY, MARK P. · 2013 to 2017
$2.9M
Noninvasive measurement of oncogenic signaling pathways with 89Zr-transferrinR00CA172695 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EVANS, MICHAEL JOHN · 2014 to 2016
$728k
NCI NIH HHS P30 CA008748NCI NIH HHS R00 CA172695NCI NIH HHS R01 CA172546NCI NIH HHS R01 CA176671
6 · The paper itself

Abstract

purposePancreatic ductal adenocarcinoma (PDAC) is one of the most deadly cancers, with a 5-year survival rate of less than 10%. Physicians often rely on biopsy or CT to guide treatment decisions, but these techniques fail to reliably measure the actions of therapeutic agents in PDAC. KRAS mutations are present in >90% of PDAC and are connected to many signaling pathways through its oncogenic cascade, including extracellular regulated kinase (ERK) and MYC. A key downstream event of MYC is transferrin receptor (TfR), which has been identified as a biomarker for cancer therapeutics and imaging. EXPERIMENTAL

designIn this study, we aimed to test whether zirconium-89 transferrin ([

resultsMice bearing iKras*p53* tumors showed significantly higher (

conclusionsOur study demonstrates that [

Indexed as

Positron-Emission TomographyAdenocarcinomaAnimalsCarcinoma, Pancreatic DuctalCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHeterograftsHumansMiceMitogen-Activated Protein Kinase 3Molecular Targeted TherapyProto-Oncogene Proteins c-mycProto-Oncogene Proteins p21(ras)RadioisotopesSignal TransductionKRAS protein, humanMitogen-Activated Protein Kinase 3MYC protein, humanProto-Oncogene Proteins c-mycProto-Oncogene Proteins p21(ras)RadioisotopesTransferrinZirconiumZirconium-89

Identifiers

PMID30228208
PMCPMC6320277
OpenAlexW2889760268

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.