Evidence map›Paper›PMID 30551210›Full record

ArticleNucleic acids research2019

Structure of a (3+1) hybrid G-quadruplex in the PARP1 promoter.

Anjali Sengar, J Jeya Vandana, Vicki S Chambers, Marco Di Antonio, Fernaldo Richtia Winnerdy, Shankar Balasubramanian, Anh Tuân Phan

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  8. NMR Screen Reveals the Diverse Structural Landscape of a G-Quadruplex Library.Chemistry (Weinheim an der Bergstrasse, Germany) · 2024
    Article
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  20. G-quadruplex DNA: a novel target for drug design.Cellular and molecular life sciences : CMLS · 2021
    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 2 countries.

Anjali SengarSchool of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
J Jeya VandanaSchool of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
Vicki S ChambersDepartment of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.
Marco Di AntonioDepartment of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.
Fernaldo Richtia WinnerdySchool of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
Shankar BalasubramanianDepartment of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.
Anh Tuân PhanSchool of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
Nanyang Technological University · SGUniversity of Cambridge · GB

Funding

Cancer Research UK 18618
6 · The paper itself

Abstract

Poly (ADP-ribose) polymerase 1 (PARP1) has emerged as an attractive target for cancer therapy due to its key role in DNA repair processes. Inhibition of PARP1 in BRCA-mutated cancers has been observed to be clinically beneficial. Recent genome-mapping experiments have identified a non-canonical G-quadruplex-forming sequence containing bulges within the PARP1 promoter. Structural features, like bulges, provide opportunities for selective chemical targeting of the non-canonical G-quadruplex structure within the PARP1 promoter, which could serve as an alternative therapeutic approach for the regulation of PARP1 expression. Here we report the G-quadruplex structure formed by a 23-nucleotide G-rich sequence in the PARP1 promoter. Our study revealed a three-layered intramolecular (3+1) hybrid G-quadruplex scaffold, in which three strands are oriented in one direction and the fourth in the opposite direction. This structure exhibits unique structural features such as an adenine bulge and a G·G·T base triple capping structure formed between the central edgewise loop, propeller loop and 5' flanking terminal. Given the highly important role of PARP1 in DNA repair and cancer intervention, this structure presents an attractive opportunity to explore the therapeutic potential of PARP1 inhibition via G-quadruplex DNA targeting.

Indexed as

G-QuadruplexesNucleic Acid ConformationAdenineDNADNA RepairGuanineHumansNuclear Magnetic Resonance, BiomolecularPoly (ADP-Ribose) Polymerase-1Promoter Regions, GeneticAdenineDNAGuaninePoly (ADP-Ribose) Polymerase-1

Identifiers

PMID30551210
PMCPMC6379715
OpenAlexW2904555329

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.