Evidence map›Paper›PMID 34638303›Full record

ArticleCancers2021

Increased Circulating Levels of Galectin Proteins in Patients with Breast, Colon, and Lung Cancer.

Bailey B Blair, Avery T Funkhouser, Jane L Goodwin, Alexander M Strigenz, Basil H Chaballout, Julie C Martin, Connie M Arthur, Christopher Ronald Funk, W Jeffery Edenfield, Anna V Blenda

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

29 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  8. Review
  9. Galectin-9-An Emerging Glyco-Immune Checkpoint Target for Cancer Therapy.International journal of molecular sciences · 2025
    Review
  10. Review
  11. Article
  12. Article
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  15. Review
  16. Article
  17. Article
  18. Review
  19. Galectin-9 in Gastroenterological Cancer.International journal of molecular sciences · 2023
    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

10 authors at 4 institutions in 1 country.

Bailey B BlairDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC 29605, USA.
Avery T FunkhouserDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC 29605, USA.
Jane L GoodwinDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC 29605, USA.
Alexander M StrigenzDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC 29605, USA.
Basil H ChaballoutDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC 29605, USA.
Julie C MartinPrisma Health Cancer Institute, Greenville, SC 29605, USA.ORCID 0000-0003-1829-4994
Connie M ArthurJoint Program in Transfusion Medicine, Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Christopher Ronald FunkDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID 0000-0002-4113-5038
W Jeffery EdenfieldPrisma Health Cancer Institute, Greenville, SC 29605, USA.
Anna V BlendaDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC 29605, USA.ORCID 0000-0001-7669-3120
University of South Carolina · USPrisma Health · USBrigham and Women's Hospital · USEmory University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Galectins are proteins with high-affinity β-galactoside-binding sites that function in a variety of signaling pathways through interactions with glycoproteins. The known contributions of galectins-1, -3, -7, -8, and -9 to angiogenesis, metastasis, cell division, and evasion of immune destruction led us to investigate the circulating levels of these galectins in cancer patients. This study compares galectin concentrations by enzyme-linked immunosorbent assay (ELISA) from each stage of breast, lung, and colon cancer. Galectins-1 and -7, which share a prototype structure, were found to have statistically significant increases in breast and lung cancer. Of the tandem-repeat galectins, galectin-8 showed no statistically significant change in these cancer types, but galectin-9 was increased in colon and lung cancer. Galectin-3 is the only chimera-type galectin and was increased in all stages of breast, colon, and lung cancer. In conclusion, there were significant differences in the galectin levels in patients with these cancers compared with healthy controls, and galectin levels did not significantly change from stage to stage. These findings suggest that further research on the roles of galectins early in disease pathogenesis may lead to novel indications for galectin inhibitors.

Indexed as

biorepositorybreastcancercolonELISAgalectinlung

Identifiers

PMID34638303
PMCPMC8508020
OpenAlexW3204083346

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.