Evidence map›Paper›PMID 24092331›Full record

ReviewCellular & molecular biology letters2013

Regulation of the unfolded protein response by microRNAs.

Sylwia Bartoszewska, Kinga Kochan, Piotr Madanecki, Arkadiusz Piotrowski, Renata Ochocka, James F Collawn, Rafal Bartoszewski

Open access · goldAbstract readReview
In one paragraph

Review in Cellular & molecular biology letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Dual RNase activity of IRE1 as a target for anticancer therapies.Journal of cell communication and signaling · 2023
    Review
  5. Review
  6. Endoplasmic Reticulum Stress Signaling and Neuronal Cell Death.International journal of molecular sciences · 2022
    Review
  7. 1, 25-(OH)Genes & genomics · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. SARS-CoV-2 may regulate cellular responses through depletion of specific host miRNAs.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  14. Article
  15. Review
  16. FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  17. Article
  18. Review
  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 at 2 institutions in 2 countries.

Sylwia Bartoszewska *Department of Inorganic Chemistry, Medical University of Gdansk, Gdansk, Poland.
Kinga Kochan *Department of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Piotr MadaneckiDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Arkadiusz PiotrowskiDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Renata OchockaDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
James F CollawnDepartment of Cell, Developmental and IntegrativeBiology, University of Alabama at Birmingham, Birmingham, USA.
Rafal BartoszewskiDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Gdańsk Medical University · PLUniversity of Alabama at Birmingham · US

Funding

Cell Biology of CFTR in Polarized EpitheliaR01DK060065 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI COLLAWN, JAMES F. · 2003 to 2013
$3.1M
NIDDK NIH HHS 1 R01-DK060065NIDDK NIH HHS R01 DK060065
6 · The paper itself

Abstract

The unfolded protein response (UPR) is an adaptive response to the stress that is caused by an accumulation of misfolded proteins in the lumen of the endoplasmic reticulum (ER). It is an important component of cellular homeostasis. During ER stress, the UPR increases the protein-folding capacity of the endoplasmic reticulum to relieve the stress. Failure to recover leads to apoptosis. Specific cellular mechanisms are required for the cellular recovery phase after UPR activation. Using bioinformatics tools, we identified a number of microRNAs that are predicted to decrease the mRNA expression levels for a number of critical components of the UPR. In this review, we discuss the potential role of microRNAs as key regulators of this pathway and describe how microRNAs may play an essential role in turning off the UPR after the stress has subsided.

Indexed as

Unfolded Protein ResponseAnimalsEndoplasmic ReticulumEndoplasmic Reticulum StressGene Expression RegulationHumansMicroRNAsMicroRNAs

Identifiers

PMID24092331
PMCPMC3877167
OpenAlexW2145807448

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.