Evidence map›Paper›PMID 28587822›Full record

ArticleBioorganic & medicinal chemistry letters2017

Initial evaluation of Cu-64 labeled PARPi-DOTA PET imaging in mice with mesothelioma.

Tao Huang, Pengcheng Hu, Anna B Banizs, Jiang He

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Current status of radionuclide therapy targeting PARP in cancer: challenges and prospects.European journal of nuclear medicine and molecular imaging · 2026
    Review
  2. Development and evaluation of aEJNMMI radiopharmacy and chemistry · 2025
    Article
  3. Review
  4. Article
  5. [Journal of clinical medicine · 2024
    Review
  6. Article
  7. [Scientific reports · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. PET Imaging of PARP Expression UsingJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    Article
  14. 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

4 authors at 2 institutions in 2 countries.

Tao HuangDepartment of Radiology and Medical Imaging, University of Virginia, Charlottesville, VA 22908, United States.
Pengcheng HuDepartment of Radiology and Medical Imaging, University of Virginia, Charlottesville, VA 22908, United States; Department of Nuclear Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Anna B BanizsDepartment of Radiology and Medical Imaging, University of Virginia, Charlottesville, VA 22908, United States.
Jiang HeDepartment of Radiology and Medical Imaging, University of Virginia, Charlottesville, VA 22908, United States. Electronic address: jh6qv@virginia.edu.
University of Virginia · USSun Yat-sen University · CN

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Targeted liposomal radiotherapy of malignant mesotheliomaR01CA135358 · NCI · UNIVERSITY OF VIRGINIA · PI HE, JIANG · 2008 to 2011
$1.0M
NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA135358
6 · The paper itself

Abstract

Poly(ADP-ribose) polymerase (PARP) has emerged as an important molecular target for the treatment of several oncological diseases. A couple of molecular probes based on Olaparib scaffold have been developed by incorporation of F-18 or fluorophore for positron emission tomography (PET) or optical imaging in several types of tumor. PARP has been reported overexpressed in mesothelioma. We hereby synthesized an analogue of Olaparib containing DOTA moiety and radiolabeled it with Cu-64 to evaluate its utility of PET tracer for mesothelioma. The Cu-64 labeling was conveniently achieved at 90% yield with final compound at >99% radiochemistry purity. The biodistribution and PET imaging were performed at 0.5, 1, 2 and 18h to confirm the in vivo tumor targeting. The tumor uptake in study group was significant higher than that in control group (3.45±0.47% ID/g vs 2.26±0.30% ID/g) and tumor were clearly detected by PET imaging. These results suggest the feasibility to develop an Olaparib-based theranostic agent for mesothelioma.

Indexed as

AnimalsCopper RadioisotopesHeterocyclic Compounds, 1-RingMaleMesotheliomaMiceMice, NudePhthalazinesPiperazinesPoly(ADP-ribose) PolymerasesPositron-Emission TomographyTissue Distribution1,4,7,10-tetraazacyclododecane- 1,4,7,10-tetraacetic acidCopper RadioisotopesHeterocyclic Compounds, 1-RingolaparibPhthalazinesPiperazinesPoly(ADP-ribose) PolymerasesImagingMesotheliomaOlaparibPARP inhibitorPET

Identifiers

PMID28587822
PMCPMC5724367
OpenAlexW2618687951

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.