Evidence map›Paper›PMID 30401887›Full record

ArticleScientific reports2018

PIWI proteins contribute to apoptosis during the UPR in human airway epithelial cells.

Magdalena Gebert, Sylwia Bartoszewska, Anna Janaszak-Jasiecka, Adrianna Moszyńska, Aleksandra Cabaj, Jarosław Króliczewski, Piotr Madanecki, Renata J Ochocka, David K Crossman, James F Collawn and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. SomaticiScience · 2025
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  6. Dual RNase activity of IRE1 as a target for anticancer therapies.Journal of cell communication and signaling · 2023
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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

11 authors at 3 institutions in 2 countries.

Magdalena GebertDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Sylwia BartoszewskaDepartment of Inorganic Chemistry, Medical University of Gdansk, Gdansk, Poland.
Anna Janaszak-JasieckaDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Adrianna MoszyńskaDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Aleksandra CabajLaboratory of Bioinformatics, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland.
Jarosław KróliczewskiDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Piotr MadaneckiDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
Renata J OchockaDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
David K CrossmanDepartment of Genetics, Heflin Center for Genomic Science, University of Alabama at Birmingham, Birmingham, USA.ORCID http://orcid.org/0000-0002-0981-169X
James F CollawnDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, USA.
Rafal BartoszewskiDepartment of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland. rafalbar@gumed.edu.pl.ORCID http://orcid.org/0000-0002-2864-6757
Gdańsk Medical University · PLUniversity of Alabama at Birmingham · USInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Brian R. Davis · 2007 to 2026
$23.0M
NIDDK NIH HHS P30 DK072482
6 · The paper itself

Abstract

Small noncoding microRNAs (miRNAs) post-transcriptionally regulate a large portion of the human transcriptome. miRNAs have been shown to play an important role in the unfolded protein response (UPR), a cellular adaptive mechanism that is important in alleviating endoplasmic reticulum (ER) stress and promoting cell recovery. Another class of small noncoding RNAs, the Piwi-interacting RNAs (piRNAs) together with PIWI proteins, was originally shown to play a role as repressors of germline transposable elements. More recent studies, however, indicate that P-element induced WImpy proteins (PIWI proteins) and piRNAs also regulate mRNA levels in somatic tissues. Using genome-wide small RNA next generation sequencing, cell viability assays, and caspase activity assays in human airway epithelial cells, we demonstrate that ER stress specifically up-regulates total piRNA expression profiles, and these changes correlate with UPR-induced apoptosis as shown by up-regulation of two pro-apoptotic factor mRNAs, CHOP and NOXA. Furthermore, siRNA knockdown of PIWIL2 and PIWIL4, two proteins involved in piRNA function, attenuates UPR-related cell death, inhibits piRNA expression, and inhibits the up-regulation of CHOP and NOXA mRNA expression. Hence, we provide evidence that PIWIL2 and PIWIL4 proteins, and potentially the up-regulated piRNAs, constitute a novel epigenetic mechanism that control cellular fate during the UPR.

Indexed as

ApoptosisEndoplasmic Reticulum StressUnfolded Protein ResponseArgonaute ProteinsBronchiCells, CulturedCell SurvivalEpithelial CellsHumansRNA InterferenceArgonaute ProteinsPIWIL1 protein, human

Identifiers

PMID30401887
PMCPMC6219583
OpenAlexW2898626030

What OpenQuestion holds

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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.