Evidence map›Paper›PMID 33103995›Full record

ArticleeLife2020

Inhibiting IRE1α-endonuclease activity decreases tumor burden in a mouse model for hepatocellular carcinoma.

Nataša Pavlović, Carlemi Calitz, Kess Thanapirom, Guiseppe Mazza, Krista Rombouts, Pär Gerwins, Femke Heindryckx

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Tumor necrosis factor α-induced endoplasmic reticulum stress promotes airway smooth muscle cell proliferation.American journal of physiology. Lung cellular and molecular physiology · 2026
    Article
  5. Article
  6. Review
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  9. Article
  10. World journal of gastroenterology · 2025
    Article
  11. Review
  12. Roles of X-box binding protein 1 in liver pathogenesis.Clinical and molecular hepatology · 2025
    Review
  13. Article
  14. Review
  15. The mammalian Ire1 inhibitor, 4μ8C, exhibits broad anti-bioRxiv : the preprint server for biology · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Unveiling the mechanisms and challenges of cancer drug resistance.Cell communication and signaling : CCS · 2024
    Review
  20. The mammalian Ire1 inhibitor, 4µ8C, exhibits broad anti-Frontiers in cellular and infection microbiology · 2024
    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.

Nataša PavlovićDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Carlemi CalitzDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Kess ThanapiromRegenerative Medicine & Fibrosis Group, Institute for Liver and Digestive Health, University College London, London, United Kingdom.
Guiseppe MazzaRegenerative Medicine & Fibrosis Group, Institute for Liver and Digestive Health, University College London, London, United Kingdom.
Krista RomboutsRegenerative Medicine & Fibrosis Group, Institute for Liver and Digestive Health, University College London, London, United Kingdom.
Pär GerwinsDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Femke HeindryckxDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-1987-7676
Uppsala University · SECystic Fibrosis Trust · GB

Funding

Cancerfonden CAN2013/1273Cancerfonden CAN 2017/518Svenska Sällskapet för Medicinsk Forskning S17-0092
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a liver tumor that usually arises in patients with cirrhosis. Hepatic stellate cells are key players in the progression of HCC, as they create a fibrotic micro-environment and produce growth factors and cytokines that enhance tumor cell proliferation and migration. We assessed the role of endoplasmic reticulum (ER) stress in the cross-talk between stellate cells and HCC cells. Mice with a fibrotic HCC were treated with the IRE1α-inhibitor 4μ8C, which reduced tumor burden and collagen deposition. By co-culturing HCC-cells with stellate cells, we found that HCC-cells activate IREα in stellate cells, thereby contributing to their activation. Inhibiting IRE1α blocked stellate cell activation, which then decreased proliferation and migration of tumor cells in different in vitro 2D and 3D co-cultures. In addition, we also observed cell-line-specific direct effects of inhibiting IRE1α in tumor cells.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, HepatocellularCell Line, TumorCell ProliferationChemotaxisCoculture TechniquesEndoribonucleasesHumansHymecromoneLiver NeoplasmsLiver Neoplasms, ExperimentalMaleMiceProtein Serine-Threonine KinasesTissue Scaffolds4-methylumbelliferone 8-carbaldehydeAntineoplastic AgentsEndoribonucleasesErn1 protein, mouseHymecromoneProtein Serine-Threonine Kinasescancer biologyendoplasmic reticulum stressfibrosishepatic stellate cellIRE1alphamousestroma

Identifiers

PMID33103995
PMCPMC7661042
OpenAlexW3094579980

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.