Evidence map›Paper›PMID 25601159›Full record

ArticleCell research2015

Tyrosine 370 phosphorylation of ATM positively regulates DNA damage response.

Hong-Jen Lee, Li Lan, Guang Peng, Wei-Chao Chang, Ming-Chuan Hsu, Ying-Nai Wang, Chien-Chia Cheng, Leizhen Wei, Satoshi Nakajima, Shih-Shin Chang and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

16 authors at 4 institutions in 4 countries.

Hong-Jen Lee1] Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA [2] The University of Texas Graduate School of Biomedical Science at Houston, Houston, TX 77030, USA.
Li Lan1] Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15213, USA [2] Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.
Guang PengDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Wei-Chao Chang1] Graduate Institute of Cancer Biology, Center for Molecular Medicine, China Medical University, Taichung 404 [2] The Genomics Research Center, Academia Sinica, Taipei 115.
Ming-Chuan HsuDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Ying-Nai Wang1] Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA [2] Graduate Institute of Cancer Biology, Center for Molecular Medicine, China Medical University, Taichung 404.
Chien-Chia ChengDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Leizhen Wei1] Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15213, USA [2] Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.
Satoshi Nakajima1] Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15213, USA [2] Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.
Shih-Shin Chang1] Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA [2] The University of Texas Graduate School of Biomedical Science at Houston, Houston, TX 77030, USA.
Hsin-Wei Liao1] Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA [2] The University of Texas Graduate School of Biomedical Science at Houston, Houston, TX 77030, USA.
Chung-Hsuan ChenThe Genomics Research Center, Academia Sinica, Taipei 115.
Martin LavinUniversity of Queensland Centre for Clinical Research, Royal Brisbane Hospital Campus, Herston, Australia.
K Kian AngDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Shiaw-Yih LinDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Mien-Chie Hung1] Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA [2] The University of Texas Graduate School of Biomedical Science at Houston, Houston, TX 77030, USA [3] Graduate Institute of Cancer Biology, Center for Molecular Medicine, China Medical University, Taichung 404 [4] Department of Biotechnology, Asia University, Taichung 404.
The University of Texas MD Anderson Cancer Center · USUniversity of Pittsburgh · USGenomics Research Center, Academia Sinica · TWUniversity of Queensland · AU

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tyrosine Kinase-Dependant and - Independent Pathways of EGFR in Breast Cancer ProP01CA099031 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HUNG, MIEN-CHIE · 2003 to 2014
$11.6M
Tumor Progression of Nuclear EGFR in Breast CancerR01CA109311 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HUNG, MIEN-CHIE · 2004 to 2014
$3.0M
Oxidative DNA base damage and repair at telomeres and the relevance to cell senesR21AG045545 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAN, LI, OPRESKO, PATRICIA L · 2013 to 2014
$422k
NCI NIH HHS CA099031NCI NIH HHS CA109311NCI NIH HHS CA16672NCI NIH HHS P01 CA099031NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA109311NIA NIH HHS AG045545-01NIA NIH HHS R21 AG045545
6 · The paper itself

Abstract

Ataxia telangiectasia mutated (ATM) mediates DNA damage response by controling irradiation-induced foci formation, cell cycle checkpoint, and apoptosis. However, how upstream signaling regulates ATM is not completely understood. Here, we show that upon irradiation stimulation, ATM associates with and is phosphorylated by epidermal growth factor receptor (EGFR) at Tyr370 (Y370) at the site of DNA double-strand breaks. Depletion of endogenous EGFR impairs ATM-mediated foci formation, homologous recombination, and DNA repair. Moreover, pretreatment with an EGFR kinase inhibitor, gefitinib, blocks EGFR and ATM association, hinders CHK2 activation and subsequent foci formation, and increases radiosensitivity. Thus, we reveal a critical mechanism by which EGFR directly regulates ATM activation in DNA damage response, and our results suggest that the status of ATM Y370 phosphorylation has the potential to serve as a biomarker to stratify patients for either radiotherapy alone or in combination with EGFR inhibition.

Indexed as

DNA RepairAmino Acid SequenceAtaxia Telangiectasia Mutated ProteinsCell Line, TumorCheckpoint Kinase 2DNA Breaks, Double-StrandedErbB ReceptorsGefitinibHeLa CellsHumansPhosphorylationQuinazolinesRadiation, IonizingRNA InterferenceRNA, Small InterferingSignal TransductionAtaxia Telangiectasia Mutated ProteinsCheckpoint Kinase 2ErbB ReceptorsGefitinibQuinazolinesRNA, Small InterferingTyrosine

Identifiers

PMID25601159
PMCPMC4650576
OpenAlexW2100647031

What OpenQuestion holds

Textmetadata
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.