Evidence map›Paper›PMID 23572207›Full record

ReviewSeminars in immunopathology2013

Potential for therapeutic manipulation of the UPR in disease.

Sang Won Park, Umut Ozcan

Open access · hybridAbstract readReview
In one paragraph

Review in Seminars in immunopathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Review
  3. Dysregulation of N-glycosylation byInternational journal of biological sciences · 2025
    Article
  4. Article
  5. FicD sensitizes cellular response to glucose fluctuations in mouse embryonic fibroblasts.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Review
  8. Endoplasmic reticulum stress: a vital process and potential therapeutic target in chronic obstructive pulmonary disease.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  9. Review
  10. Article
  11. Mechanistic Research into the Effects of the Jianpi Xiaozhi Formula on Liver Injury in Diabetic Rats.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Emerging Roles of BRD7 in Pathophysiology.International journal of molecular sciences · 2020
    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

2 authors at 2 institutions in 1 country.

Sang Won ParkDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Umut Ozcan
Boston Children's Hospital · USHarvard University · US

Funding

The In Vivo Role of JNK-1 and IRS-1 Ser307 Phosphorylation In Development of InsuR01DK081009 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI OZCAN, UMUT · 2008 to 2012
$1.7M
The role of BRD7 in the regulation of endoplasmic reticulum and glucose homeostasK99DK093788 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI PARK, SANG WON · 2012 to 2013
$180k
NIDDK NIH HHS K99 DK093788NIDDK NIH HHS K99DK093788NIDDK NIH HHS R01 DK081009NIDDK NIH HHS R01DK081009
6 · The paper itself

Abstract

Increased endoplasmic reticulum (ER) stress and the activated unfolded protein response (UPR) signaling associated with it play key roles in physiological processes as well as under pathological conditions. The UPR normally protects cells and re-establishes cellular homeostasis, but prolonged UPR activation can lead to the development of various pathologies. These features make the UPR signaling pathway an attractive target for the treatment of diseases whose pathogenesis is characterized by chronic activation of this pathway. Here, we focus on the molecular signaling pathways of the UPR and suggest possible ways to target this response for therapeutic purposes.

Indexed as

Unfolded Protein ResponseAnimalsDrug TherapyEndoplasmic ReticulumEndoplasmic Reticulum StressHumansMolecular ChaperonesMolecular Chaperones

Identifiers

PMID23572207
PMCPMC3641308
OpenAlexW2151574490

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.