Evidence map›Paper›PMID 26979393›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2016

Molecular Pathways: Immunosuppressive Roles of IRE1α-XBP1 Signaling in Dendritic Cells of the Tumor Microenvironment.

Juan R Cubillos-Ruiz, Sarah E Bettigole, Laurie H Glimcher

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.7field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 43 citations in OpenAlex.

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  8. Emerging role of IRE1α in vascular diseases.Journal of cell communication and signaling · 2024
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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

3 authors at 1 institution in 1 country.

Juan R Cubillos-RuizDepartment of Obstetrics and Gynecology, Weill Cornell Medical College, New York, New York. Sandra and Edward Meyer Cancer Center, Weill Cornell Medical College, New York, New York. jur2016@med.cornell.edu lglimche@med.cornell.edu.
Sarah E BettigoleSandra and Edward Meyer Cancer Center, Weill Cornell Medical College, New York, New York. Department of Medicine, Weill Cornell Medical College, New York, New York.
Laurie H GlimcherSandra and Edward Meyer Cancer Center, Weill Cornell Medical College, New York, New York. Department of Medicine, Weill Cornell Medical College, New York, New York. jur2016@med.cornell.edu lglimche@med.cornell.edu.
Cornell University · US

Funding

T-bet and Tumor ImmunityR01CA112663 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GLIMCHER, LAURIE HOLLIS · 2005 to 2015
$3.3M
From Sugar to Fat: How Transcription Factor XBP1 Regulates Hepatic LipogenesisR01DK082448 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI GLIMCHER, LAURIE HOLLIS · 2010 to 2014
$1.7M
NCI NIH HHS R01 CA112663NIDDK NIH HHS R01 DK082448
6 · The paper itself

Abstract

The endoplasmic reticulum (ER) is a massive cytoplasmic membrane network that functions primarily to ensure proper folding and posttranslational modification of newly synthesized secreted and transmembrane proteins. Abnormal accumulation of unfolded proteins in this organelle causes a state of "ER stress," which is a hallmark feature of various diseases, including cancer, neurodegeneration, and metabolic dysfunction. Cancer cells exploit the IRE1α-XBP1 arm of the ER stress response to efficiently adjust their protein-folding capacity and ensure survival under hostile tumor microenvironmental conditions. However, we recently found that dendritic cells (DC) residing in the ovarian cancer microenvironment also experience sustained ER stress and demonstrate persistent activation of the IRE1α-XBP1 pathway. This previously unrecognized process disrupts metabolic homeostasis and antigen-presenting capacity in DCs, thereby crippling their natural ability to support the protective functions of infiltrating antitumor T cells. In this review, we briefly discuss some of the mechanisms that fuel ER stress in tumor-associated DCs, the biologic processes altered by aberrant IRE1α-XBP1 signaling in these innate immune cells, and the unique immunotherapeutic potential of targeting this pathway in cancer hosts. Clin Cancer Res; 22(9); 2121-6. ©2016 AACR.

Indexed as

AnimalsDendritic CellsEndoplasmic ReticulumEndoplasmic Reticulum StressEndoribonucleasesHumansImmune ToleranceProtein Serine-Threonine KinasesSignal TransductionTumor MicroenvironmentX-Box Binding Protein 1EndoribonucleasesERN1 protein, humanProtein Serine-Threonine KinasesX-Box Binding Protein 1XBP1 protein, human

Identifiers

PMID26979393
PMCPMC4854763
OpenAlexW2297773450

What OpenQuestion holds

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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.