Evidence map›Paper›PMID 19579069›Full record

ReviewInternational journal of radiation biology2009

Response of heterogeneous ribonuclear proteins (hnRNP) to ionising radiation and their involvement in DNA damage repair.

Benjamin Haley, Tatjana Paunesku, Miroslava Protić, Gayle E Woloschak

Open access · greenAbstract readReview
In one paragraph

Review in International journal of radiation biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

51 citing papers in PubMed, 77 citations in OpenAlex.

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  12. The role of Cold-Inducible RNA-binding protein in respiratory diseases.Journal of cellular and molecular medicine · 2022
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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

4 authors at 3 institutions in 1 country.

Benjamin HaleyDepartment of Radiation Oncology, Northwestern University, Chicago, Illinois, USA.
Tatjana Paunesku
Miroslava Protić
Gayle E Woloschak
Northwestern University · USArgonne National Laboratory · USRadiation Oncology Institute · US

Funding

TiO2 nanocomposites for Targeted Treatment and Imaging of Prostate cancerU54CA119341 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A. · 2005 to 2009
$19.9M
THEILER'S VIRUS NEUROTROPISM AND NEUROVIRULENCEP01NS021442 · NINDS · UNIVERSITY OF CHICAGO · PI ROOS, RAYMOND PHILIP · 1985 to 2002
$3.0M
Applications of TiO2-DNA nanocompositesR01EB002100 · NIBIB · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WOLOSCHAK, GAYLE E. · 2005 to 2013
$2.5M
PCNA PROMOTER DELETION IN RADIOSENSITIVE MICER01CA081375 · NCI · UNIVERSITY OF CHICAGO · PI WOLOSCHAK, GAYLE E · 2000 to 2003
$1.1M
Application of TiO2-DNA nanocomposites to Cancer CellsR01CA107467 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WOLOSCHAK, GAYLE E. · 2004 to 2006
$960k
VIRAL MOTOR NEURONAL TROPISM AND NEUROVIRULENCEP50NS021442 · NINDS · UNIVERSITY OF CHICAGO · PI ROOS, RAYMOND PHILIP · 1988 to 1997
–
NCI NIH HHS R01 CA081375NCI NIH HHS R01 CA107467NCI NIH HHS U54 CA119341NCI NIH HHS U54CA119341NIBIB NIH HHS EB002100NIBIB NIH HHS R01 EB002100NINDS NIH HHS NS21442-18NINDS NIH HHS P01 NS021442
6 · The paper itself

Abstract

purposeTo determine the relationship between heterogeneous nuclear ribonucleoproteins (hnRNP) and DNA repair, particularly in response to ionising radiation (IR). MATERIALS AND

methodsThe literature was examined for papers related to the topics of hnRNP, IR and DNA repair.

resultsHnRNP orchestrate the processing of mRNA to which they are bound in response to IR. HnRNP A18, B1, C1/C2 and K interact with important proteins from DNA Damage Response (DDR) pathways, binding DNA-dependent protein kinase (DNA-PK), the Ku antigen (Ku) and tumour suppressor protein 53 (p53) respectively. Notably, irregularities in the expression of hnRNP A18, B1, K, P2 and L have been linked to cancer and radiosensitivity. Sixteen different hnRNP proteins have been reported to show either mRNA transcript or protein quantity changes following IR. Various protein modifications of hnRNP in response to IR have also been noted: hnRNP A18, C1/C2 and K are phosphorylated; hnRNP C1/C2 is a target of apoptotic proteases; and hnRNP K degradation is controlled by murine double minute ubiquitin ligase (MDM2). Evidence points to a role for hnRNP A1, A18, A2/B1, C1/C2, K and P2 in regulating double-stranded break (DSB) repair pathways by promoting either homologous recombination (HR) or non-homologous end rejoining (NHEJ) repair pathways following IR.

conclusionsHnRNP proteins play a pivotal role in coordinating repair pathways following exposure to IR, through protein-protein interactions and transcript regulation of key repair and stress response mRNA. In particular, several hnRNP proteins are critical in coordinating the choice of HR or NHEJ to repair DSB caused by IR.

Indexed as

DNA RepairAnimalsDNADNA DamageHeterogeneous-Nuclear RibonucleoproteinsHumansRadiation, IonizingRecombination, GeneticDNAHeterogeneous-Nuclear Ribonucleoproteins

Identifiers

PMID19579069
PMCPMC2785495
OpenAlexW2130036151

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.