Evidence map›Paper›PMID 27814504›Full record

ArticleCell2016

Inflammation Improves Glucose Homeostasis through IKKβ-XBP1s Interaction.

Junli Liu, Dorina Ibi, Koji Taniguchi, Jaemin Lee, Hilde Herrema, Bedia Akosman, Patrick Mucka, Mario Andres Salazar Hernandez, Muhemmet Fatih Uyar, Sang Won Park and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

62 citing papers in PubMed, 90 citations in OpenAlex.

  1. Trial
  2. RNase L Regulates Antiviral Responsiveness through Cleavage of XBP1 mRNA.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
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  5. Chronic succinate exposure does not cause liver injury.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. Emerging role of IRE1α in vascular diseases.Journal of cell communication and signaling · 2024
    Review
  10. Turnover of EDEM1, an ERAD-enhancing factor, is mediated by multiple degradation routes.Genes to cells : devoted to molecular & cellular mechanisms · 2024
    Article
  11. Review
  12. Cancer Metabolism under Limiting Oxygen Conditions.Cold Spring Harbor perspectives in medicine · 2024
    Review
  13. Article
  14. Ubiquitination and Metabolic Disease.Advances in experimental medicine and biology · 2024
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

2 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 1 country.

Junli LiuDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Dorina IbiDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Koji TaniguchiLaboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, San Diego, CA 92093, USA; Department of Pathology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, San Diego, CA 92093, USA.
Jaemin LeeDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Hilde HerremaDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Bedia AkosmanDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Patrick MuckaDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Mario Andres Salazar HernandezDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Muhemmet Fatih UyarDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Sang Won ParkDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA.
Michael KarinLaboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, San Diego, CA 92093, USA; Department of Pathology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, San Diego, CA 92093, USA.
Umut OzcanDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02130, USA. Electronic address: umut.ozcan@childrens.harvard.edu.
Boston Children's Hospital · USHarvard University · USUniversity of California, San Diego · US

Funding

Tumor Assessment CoreP01CA128814 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI SMITH, JEFFREY W · 2009 to 2020
$19.1M
REGULATION OF NFKB AND IKK BY PROINFLAMMATORY STIMULIR01AI043477 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KARIN, MICHAEL · 1998 to 2017
$7.4M
NF-kappaB and Mitochondrial Signals as Positive and Negative Regulators of InflammationR37AI043477 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Michael Karin · 2018 to 2026
$6.0M
Endoplasmic Reticulum Stress, Brain and ObesityR01DK098496 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI OZCAN, UMUT · 2013 to 2022
$4.6M
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
NCI NIH HHS P01 CA128814NIAID NIH HHS R01 AI043477NIAID NIH HHS R37 AI043477NIDDK NIH HHS R01 DK081009NIDDK NIH HHS R01 DK098496
6 · The paper itself

Abstract

It is widely believed that inflammation associated with obesity has an important role in the development of type 2 diabetes. IκB kinase beta (IKKβ) is a crucial kinase that responds to inflammatory stimuli such as tumor necrosis factor α (TNF-α) by initiating a variety of intracellular signaling cascades and is considered to be a key element in the inflammation-mediated development of insulin resistance. We show here, contrary to expectation, that IKKβ-mediated inflammation is a positive regulator of hepatic glucose homeostasis. IKKβ phosphorylates the spliced form of X-Box Binding Protein 1 (XBP1s) and increases the activity of XBP1s. We have used three experimental approaches to enhance the IKKβ activity in the liver of obese mice and observed increased XBP1s activity, reduced ER stress, and a significant improvement in insulin sensitivity and consequently in glucose homeostasis. Our results reveal a beneficial role of IKKβ-mediated hepatic inflammation in glucose homeostasis.

Indexed as

Endoplasmic Reticulum StressAnimalsCell Line, TumorDiabetes Mellitus, Type 2GlucoseHomeostasisHumansI-kappa B KinaseLiverMaleMiceMice, Inbred C57BLMice, ObeseObesityPhosphorylationProtein StabilityGlucoseI-kappa B KinaseIkbkb protein, mouseX-Box Binding Protein 1Xbp1 protein, mousediabetesER stressglucose metabolismIKKβinflammationinsulin resistanceobesityunfolded protein responseUPRXBP1s

Identifiers

PMID27814504
PMCPMC5908236
OpenAlexW2548784951

What OpenQuestion holds

Textmetadata
LicenceTDM
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.