Evidence map›Paper›PMID 21891782›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2011

p73 protein regulates DNA damage repair.

Elena Zaika, Jinxiong Wei, Dengping Yin, Claudia Andl, Ute Moll, Wael El-Rifai, Alexander I Zaika

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Article
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  8. Review
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  11. Article
  12. Review
  13. Review: immunoassays in DNA damage and instability detection.Cellular and molecular life sciences : CMLS · 2019
    Review
  14. Article
  15. Review
  16. Gastroesophageal Reflux Induces Protein Adducts in the Esophagus.Cellular and molecular gastroenterology and hepatology · 2019
    Article
  17. Review
  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

7 authors.

Elena ZaikaDepartment of Surgery, Vanderbilt University Medical Center, 1255 Light Hall, 2215 Garland Ave., Nashville, TN 37232, USA.
Jinxiong Wei
Dengping Yin
Claudia Andl
Ute Moll
Wael El-Rifai
Alexander I Zaika

Funding

Regulation of the Oncogenic Stress Response in Helicobacter pylori-infected cellsR01CA138833 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALEXANDER I. ZAIKA · 2010 to 2026
$4.3M
Molecular Pathobiology of Barrett's TumorigenesisR01CA106176 · NCI · VANDERBILT UNIVERSITY · PI EL-RIFAI, WAEL · 2003 to 2014
$3.3M
The Role of p73 in Upper Gastrointestinal CarcinomasR01CA108956 · NCI · VANDERBILT UNIVERSITY · PI ZAIKA, ALEXANDER I. · 2005 to 2010
$1.3M
E-cadherin regulates TGFb receptor type II biology and functionK01DK075379 · NIDDK · VANDERBILT UNIVERSITY · PI ANDL, CLAUDIA D · 2007 to 2011
$661k
Regulation of gastroesophageal reflux-associated tumorigenesisI01BX002115 · VA · VETERANS HEALTH ADMINISTRATION · PI ZAIKA, ALEXANDER I. · 2014 to 2024
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NCI NIH HHS R01 CA106176NCI NIH HHS R01CA106176NCI NIH HHS R01 CA108956NCI NIH HHS R01 CA138833NCI NIH HHS R01CA138833NIDDK NIH HHS K01 DK075379
6 · The paper itself

Abstract

Although the p53 tumor suppressor is relatively well characterized, much less is known about the functions of other members of the p53 family, p73 and p63. Here, we present evidence that in specific pathological conditions caused by exposure of normal cells to bile acids in acidic conditions, p73 protein plays the predominant role in the DNA damage response. These pathological conditions frequently occur during gastric reflux in the human esophagus and are associated with progression to esophageal adenocarcinoma. We found that despite strong DNA damage induced by bile acid exposure, only p73 (but not p53 and p63) is selectively activated in a c-Abl kinase-dependent manner. The activated p73 protein induces DNA damage repair. Using a human DNA repair PCR array, we identified multiple DNA repair genes affected by p73. Two glycosylases involved in base excision repair, SMUG1 and MUTYH, were characterized and found to be transcriptionally regulated by p73 in DNA damage conditions. Using a surgical procedure in mice, which recapitulates bile acid exposure, we found that p73 deficiency is associated with increased DNA damage. These findings were further investigated with organotypic and traditional cell cultures. Collectively our studies demonstrate that p73 plays an important role in the regulation of DNA damage repair.

Indexed as

DNA DamageAnimalsBase SequenceBile Acids and SaltsCells, CulturedDNA-Binding ProteinsDNA GlycosylasesDNA PrimersDNA RepairEsophageal NeoplasmsGastroesophageal RefluxHumansMiceModels, BiologicalNuclear ProteinsTumor Protein p73Bile Acids and SaltsDNA-Binding ProteinsDNA GlycosylasesDNA PrimersmutY adenine glycosylaseNuclear ProteinsSMUG1 protein, humanTP73 protein, humanTrp73 protein, mouseTumor Protein p73Tumor Suppressor ProteinsUracil-DNA Glycosidase

Identifiers

PMID21891782
PMCPMC3236618

What OpenQuestion holds

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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.