Evidence map›Paper›PMID 36438061›Full record

ReviewFrontiers in medicine2022

Poly (ADP-ribose) polymerases as PET imaging targets for central nervous system diseases.

Jie Tong, Baosheng Chen, Peng Wen Tan, Stephen Kurpiewski, Zhengxin Cai

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Imaging poly(ADP-ribose) polymerase-1 (PARP1)Acta pharmaceutica Sinica. B · 2025
    Article
  3. 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

5 authors at 1 institution in 1 country.

Jie TongYale PET Center, Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States.
Baosheng ChenYale PET Center, Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States.
Peng Wen TanYale PET Center, Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States.
Stephen KurpiewskiYale PET Center, Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States.
Zhengxin CaiYale PET Center, Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States.
Yale Cancer Center · US

Funding

Development of novel CXCR5 PET Imaging probe for Angioimmunoblastic T-cell LymphomaR21CA252587 · NCI · YALE UNIVERSITY · PI CAI, ZHENGXIN · 2020 to 2020
$431k
Brain Penetrant PARP Targeted PET Imaging ProbesR03CA249569 · NCI · YALE UNIVERSITY · PI CAI, ZHENGXIN · 2020 to 2021
$250k
NCI NIH HHS R03 CA249569NCI NIH HHS R21 CA252587
6 · The paper itself

Abstract

Poly (ADP-ribose) polymerases (PARPs) constitute of 17 members that are associated with divergent cellular processes and play a crucial role in DNA repair, chromatin organization, genome integrity, apoptosis, and inflammation. Multiple lines of evidence have shown that activated PARP1 is associated with intense DNA damage and irritating inflammatory responses, which are in turn related to etiologies of various neurological disorders. PARP1/2 as plausible therapeutic targets have attracted considerable interests, and multitudes of PARP1/2 inhibitors have emerged for treating cancer, metabolic, inflammatory, and neurological disorders. Furthermore, PARP1/2 as imaging targets have been shown to detect, delineate, and predict therapeutic responses in many diseases by locating and quantifying the expression levels of PARP1/2. PARP1/2-directed noninvasive positron emission tomography (PET) has potential in diagnosing and prognosing neurological diseases. However, quantitative PARP PET imaging in the central nervous system (CNS) has evaded us due to the challenges of developing blood-brain barrier (BBB) penetrable PARP radioligands. Here, we review PARP1/2's relevance in CNS diseases, summarize the recent progress on PARP PET and discuss the possibilities of developing novel PARP radiotracers for CNS diseases.

Indexed as

BBBneurodegenerative diseasePARP1positron emission tomographyradiotracers

Identifiers

PMID36438061
PMCPMC9685622
OpenAlexW4308869051

What OpenQuestion holds

Textmetadata
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.