Evidence map›Paper›PMID 41298424›Full record

ArticleNature communications2025

Defining the role of β-cell IRE1α/XBP1 pathway and its gene regulatory network components in non-obese diabetic mice.

Hugo Lee, Khagani Eynullazada, Qiaodan Ou, Junha Shin, Sushmita Roy, Feyza Engin

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Deletion of the T1D risk geneBiochemistry and biophysics reports · 2026
    Article
  2. Article
  3. Review
  4. 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

6 authors.

Hugo LeeDepartment of Biomolecular Chemistry, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, USA.
Khagani Eynullazada *Wisconsin Institute for Discovery, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, USA.
Qiaodan Ou *Department of Biomolecular Chemistry, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, USA.
Junha ShinWisconsin Institute for Discovery, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, USA.ORCID http://orcid.org/0000-0003-3175-3446
Sushmita RoyWisconsin Institute for Discovery, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, USA.ORCID http://orcid.org/0000-0002-3694-1705
Feyza EnginDepartment of Biomolecular Chemistry, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, USA. fengin@wisc.edu.ORCID http://orcid.org/0000-0002-7987-5381

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Lu Mao · 1985 to 2026
$142.6M
GRADUATE TRAINING IN MOLECULAR BIOSCIENCEST32GM007215 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HULL, CHRISTINA M · 1985 to 2018
$22.5M
The role of beta cell ATF6 in type 1 diabetesR01DK130919 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI Feyza Engin · 2021 to 2026
$2.7M
Defining gene regulatory networks controlling cell fateR01GM144708 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI ROY, SUSHMITA · 2022 to 2025
$1.3M
BD FACSymphony High Parameter Flow CytometerS10OD025225 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI PATANKAR, MANISH S · 2018 to 2018
$600k
Metabolic basis of beta cell stress adaptationR56DK128136 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI ENGIN, FEYZA · 2021 to 2021
$194k
JDRF 3-SRA-2023-1315-S-B and 3-SRA-2025-1654-S-B)NCI NIH HHS P30 CA014520NIDDK NIH HHS R01 DK130919NIDDK NIH HHS R56 DK128136NIGMS NIH HHS R01 GM144708NIGMS NIH HHS T32 GM007215NIH HHS S10 OD025225
6 · The paper itself

Abstract

The unfolded protein response sensor, IRE1α, acts through its regulated IRE1α-dependent decay (RIDD) activity or transcription factor XBP1 to determine cell fate and survival. While blunting RIDD activity prevents diabetes in type 1 diabetes preclinical model non-obese diabetic mice, β-cell-specific function of XBP1 at different stages of disease remains unknown. Here we show that deletion of Xbp1 in β-cells (Xbp1

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1EndoribonucleasesGene Regulatory NetworksInsulin-Secreting CellsProtein Serine-Threonine KinasesX-Box Binding Protein 1AnimalsApoptosisMaleMiceMice, Inbred C57BLMice, Inbred NODMice, KnockoutSignal TransductionUnfolded Protein ResponseEndoribonucleasesErn1 protein, mouseProtein Serine-Threonine KinasesX-Box Binding Protein 1Xbp1 protein, mouse

Identifiers

PMID41298424
PMCPMC12657516

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.