Evidence map›Paper›PMID 23976954›Full record

ArticlePloS one2013

Nimotuzumab enhances the radiosensitivity of cancer cells in vitro by inhibiting radiation-induced DNA damage repair.

Yuan-yuan Qu, Song-liu Hu, Xiang-ying Xu, Rui-zhi Wang, Hong-yang Yu, Jian-yu Xu, Lin Chen, Guang-lu Dong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-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

27 citing papers in PubMed, 47 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

8 authors at 4 institutions in 1 country.

Yuan-yuan QuDepartment of Radiation Oncology, the Third Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Song-liu Hu
Xiang-ying Xu
Rui-zhi Wang
Hong-yang Yu
Jian-yu Xu
Lin Chen
Guang-lu Dong
Third Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CNHeilongjiang Institute of Wood Science · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNimotuzumab is a humanized IgG1 monoclonal antibody specifically targeting EGFR. In this study, we aimed to investigate the molecular mechanisms of nimotuzumab in its effects of enhancing cancer cell radiosensitivity. PRINCIPAL FINDING: Lung cancer A549 cells and breast cancer MCF-7 cells were pretreated with or without nimotuzumab for 24 h before radiation to perform the clonogenic survival assay and to analyze the cell apoptosis by flow ctyometry. γ-H2AX foci were detected by confocal microscopy to assess the effect of nimotuzumab on radiation induced DNA repair. EGFR activation was examined and the levels of DNA damage repair related proteins in A549 cells at different time point and at varying doses exposure after nimotuzumab and radiation treatment were examined by Western blot. Pretreatment with nimotuzumab reduced clonogenic survival after radiation, inhibited radiation-induced EGFR activation and increased the radiation-induced apoptosis in both A549 cells and MCF-7 cells. The foci of γ-H2AX 24 h after radiation significantly increased in nimotuzumab pretreated cells with different doses. The phosphorylation of AKT and DNA-PKcs were remarkably inhibited in the combination group at each dose point as well as time point.

conclusionsOur results revealed that the possible mechanism of nimotuzumab enhancing the cancer radiosensitivity is that nimotuzumab inhibited the radiation-induced activation of DNA-PKcs through blocking the PI3K/AKT pathway, which ultimately affected the DNA DSBs repair.

Indexed as

Antibodies, Monoclonal, HumanizedApoptosisCell Line, TumorCell SurvivalDNA-Activated Protein KinaseDNA DamageDNA RepairDose-Response Relationship, DrugErbB ReceptorsGamma RaysGene Expression RegulationHistonesHumansNuclear ProteinsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsAntibodies, Monoclonal, HumanizedDNA-Activated Protein KinaseEGFR protein, humanErbB ReceptorsH2AX protein, humanHistonesnimotuzumabNuclear ProteinsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPRKDC protein, humanProto-Oncogene Proteins c-akt

Identifiers

PMID23976954
PMCPMC3745376
OpenAlexW1977015645

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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.