Evidence map›Paper›PMID 26802028›Full record

ArticleOncotarget2016

XIAP-associating factor 1, a transcriptional target of BRD7, contributes to endothelial cell senescence.

Jong-Ik Heo, Wonwoo Kim, Kyu Jin Choi, Sangwoo Bae, Jae-Hoon Jeong, Kwang Seok Kim

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Cardiovascular ramifications of therapy-induced endothelial cell senescence in cancer survivors.Biochimica et biophysica acta. Molecular basis of disease · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Emerging Roles of BRD7 in Pathophysiology.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. 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

6 authors at 1 institution in 1 country.

Jong-Ik HeoDivisions of Radiation Effects, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Wonwoo KimResearch Center for Radiotherapy, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Kyu Jin ChoiDivisions of Radiation Effects, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Sangwoo BaeDivisions of Radiation Effects, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Jae-Hoon JeongResearch Center for Radiotherapy, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Kwang Seok KimDivisions of Radiation Effects, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Korea Institute of Radiological and Medical Sciences · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked inhibitor of apoptosis (XIAP)-associated factor 1 (XAF1) is well known as an antagonist of XIAP-mediated caspase inhibition. Although XAF1 serves as a tumor-suppressor gene, the role of XAF1 in cellular senescence remains unclear. We found that XAF1 expression was increased by genotoxic agents, such as doxorubicin and ionizing radiation in pulmonary microvascular endothelial cells, consequently leading to premature senescence. Conversely, downregulation of XAF1 in premature senescent cells partially overcame endothelial cell senescence. p53 knockdown, but not p16 knockdown, abolished senescence phenotypes caused by XAF1 induction. XAF1 expression was transcriptionally regulated by Bromodomain 7 (BRD7). XAF1 induction with interferon-gamma (IFN-γ) treatment was abrogated by BRD7 knockdown, which resulted in blocking interferon-induced senescence. In lung cancer cells, XAF1 tumor suppressor activity was decreased by BRD7 knockdown, and inhibition of tumor growth by IFN-γ did not appear in BRD7-depleted xenograft tumors. These data suggest that XAF1 is involved in BRD7-associated senescence and plays an important role in the regulation of endothelial senescence through a p53-dependent pathway. Furthermore, regulation of the BRD7/XAF1 system might contribute to tissue or organismal aging and protection against cellular transformation.

Indexed as

Bromodomain Containing ProteinsCell Line, TumorCellular SenescenceChromosomal Proteins, Non-HistoneEndothelial CellsHumansNeoplasm ProteinsTransfectionX-Linked Inhibitor of Apoptosis ProteinBRD7 protein, humanBromodomain Containing ProteinsChromosomal Proteins, Non-HistoneNeoplasm ProteinsXIAP protein, humanX-Linked Inhibitor of Apoptosis ProteinBRD7cellular senescenceDNA damageGerotargetionizing radiationp53XAF1

Identifiers

PMID26802028
PMCPMC4868675
OpenAlexW2256659800

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.