Evidence map›Paper›PMID 37531469›Full record

ArticleBiochemistry2023

Slow Dissociation from the PARP1-HPF1 Complex Drives Inhibitor Potency.

Petra Stojanovic, Karolin Luger, Johannes Rudolph

Open access · hybridAbstract read
In one paragraph

Article in Biochemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

6 citing papers in PubMed, 16 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

3 authors at 2 institutions in 1 country.

Petra StojanovicDepartment of Biochemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
Karolin LugerDepartment of Biochemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
Johannes RudolphDepartment of Biochemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.ORCID 0000-0003-0230-3323
University of Colorado Boulder · USHoward Hughes Medical Institute · US

Funding

Structure and Mechanism of Chromatin-Bound PARP1R01CA218255 · NCI · UNIVERSITY OF COLORADO · PI Karolin Luger · 2017 to 2026
$4.5M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA218255
6 · The paper itself

Abstract

PARP1, upon binding to damaged DNA, is activated to perform poly ADP-ribosylation (PARylation) on itself and other proteins, which leads to relaxation of chromatin and recruitment of DNA repair factors. HPF1 was recently discovered as a protein cofactor of PARP1 that directs preferential PARylation of histones over other targets by contributing to and altering the PARP1 active site. Inhibitors of PARP1 (PARPi) are used in the treatment of BRCA-/- cancers, but the basis for their potency in cells, especially in the context of HPF1, is not fully understood. Here, we demonstrate the simple one-step association for eight different PARPi to PARP1 with measured rates of association (

Indexed as

DNA DamageHistonesDNA RepairPhthalazinesPoly (ADP-Ribose) Polymerase-1Poly ADP RibosylationfluzoparibHistonesPhthalazinesPoly (ADP-Ribose) Polymerase-1

Identifiers

PMID37531469
PMCPMC10433523
OpenAlexW4385480307

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.