Evidence map›Paper›PMID 28195343›Full record

ReviewHepatology (Baltimore, Md.)2017

Galectin-9: Diverse roles in hepatic immune homeostasis and inflammation.

Lucy Golden-Mason, Hugo R Rosen

Open access · bronzeAbstract readReview
In one paragraph

Review in Hepatology (Baltimore, Md.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Galectin-9-An Emerging Glyco-Immune Checkpoint Target for Cancer Therapy.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Review
  8. Galectins and Liver Diseases.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
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

2 authors at 1 institution in 1 country.

Lucy Golden-MasonDivision of Gastroenterology & Hepatology, University of Colorado Denver Medical Center, Aurora, CO.
Hugo R RosenDivision of Gastroenterology & Hepatology, University of Colorado Denver Medical Center, Aurora, CO.
University of Colorado Denver · US

Funding

Human Group 2 Innate Lympohocyte Cell (ILC2) populations contribute to Hepatic FibrosisR01DK106491 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI GOLDEN, LUCY MARY · 2015 to 2019
$1.8M
RESUBMISSION -R01 AI120622 –Restoration of Immunity and Function with DAA Treatment in HCV infectionR01AI120622 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROSEN, HUGO RAMON · 2017 to 2020
$1.6M
INNATE AND ADAPTIVE IMMUNITY TO HCV IN HUMAN PREGNANCYR01HD075549 · NICHD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROSEN, HUGO RAMON · 2014 to 2018
$1.6M
Hepatitis C viral sensing by non-parenchymal liver cells (NPC)R21AI103361 · NIAID · UNIVERSITY OF COLORADO DENVER · PI ROSEN, HUGO RAMON · 2013 to 2014
$411k
NIAID NIH HHS R01 AI120622NIAID NIH HHS R21 AI103361NICHD NIH HHS R01 HD075549NIDDK NIH HHS R01 DK106491
6 · The paper itself

Abstract

Glycan-binding proteins, which include galectins, are involved at all stages of immunity and inflammation, from initiation through resolution. Galectin-9 (Gal-9) is highly expressed in the liver and has a wide variety of biological functions in innate and adaptive immunity that are instrumental in the maintenance of hepatic homeostasis. In the setting of viral hepatitis, increased expression of Gal-9 drives the expansion of regulatory T cells and contraction of effector T cells, thereby favoring viral persistence. The dichotomous nature of Gal-9 is evident in hepatocellular carcinoma, where loss of expression in hepatocytes promotes tumor growth and metastasis, whereas overexpression by Kupffer cells and endothelial cells inhibits the antitumor immune response. In nonalcoholic fatty liver disease, Gal-9 is involved indirectly in the expansion of protective natural killer T-cell populations. In ischemic liver injury, hepatocyte-derived Gal-9 is both diagnostic and cytoprotective. In drug-induced acute liver failure, plasma levels correlate with outcome. Here, we offer a synthesis of recent and emerging findings on Gal-9 in the regulation of hepatic inflammation. Ongoing studies are warranted to better elucidate the pathophysiology of hepatic immune-mediated diseases and to develop new therapeutic interventions using glycan-binding proteins. (Hepatology 2017;66:271-279).

Indexed as

Adaptive ImmunityAnimalsCarcinoma, HepatocellularGalectinsHepatitisHepatitis, AutoimmuneHomeostasisHumansImmunity, InnateLiver DiseasesLiver Diseases, AlcoholicLiver Failure, AcuteLiver NeoplasmsSensitivity and SpecificityGalectins

Identifiers

PMID28195343
PMCPMC5521806
OpenAlexW2587924565

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.