Evidence map›Paper›PMID 27496330›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Nuclear repartitioning of galectin-1 by an extracellular glycan switch regulates mammary morphogenesis.

Ramray Bhat, Brian Belardi, Hidetoshi Mori, Peiwen Kuo, Andrew Tam, William C Hines, Quynh-Thu Le, Carolyn R Bertozzi, Mina J Bissell

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.0field-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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
    Pooled it
  2. Article
  3. Nuclear Galectin-1 promotesProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Reuniting philosophy and science to advance cancer research.Biological reviews of the Cambridge Philosophical Society · 2023
    Article
  8. Galectin expression detected byEuropean journal of nuclear medicine and molecular imaging · 2022
    Article
  9. Article
  10. Article
  11. N-terminal tail prolines of Gal-3 mediate its oligomerization/phase separation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Observational
  13. First Evidence for a Role of Siglec-8 in Breast Cancer.International journal of molecular sciences · 2021
    Article
  14. Article
  15. Nanomotors Sense Local Physicochemical Heterogeneities in Tumor Microenvironments*.Angewandte Chemie (International ed. in English) · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

9 authors at 4 institutions in 1 country.

Ramray BhatLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720; ramray@mrdg.iisc.ernet.in bertozzi@stanford.edu mjbissell@lbl.gov.
Brian BelardiDepartment of Chemistry, University of California, Berkeley, CA 94720;
Hidetoshi MoriLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720; Department of Pathology, Center for Comparative Medicine, University of California, Davis, CA, 95616;
Peiwen KuoDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, 94305;
Andrew TamLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720;
William C HinesLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720;
Quynh-Thu LeDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, 94305;
Carolyn R BertozziDepartment of Chemistry, Stanford University, Stanford, CA 94305-4401; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305-4401 ramray@mrdg.iisc.ernet.in bertozzi@stanford.edu mjbissell@lbl.gov.
Mina J BissellLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720; ramray@mrdg.iisc.ernet.in bertozzi@stanford.edu mjbissell@lbl.gov.
Lawrence Berkeley National Laboratory · USStanford University · USUniversity of California, Berkeley · USUniversity of California, Davis · US

Funding

Definition of the Microenvironment in Breast CancerR01CA064786 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI BISSELL, MINA · 1995 to 2020
$6.1M
Investigations of Golgi EnzymesR01GM059907 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BERTOZZI, CAROLYN · 1999 to 2016
$5.9M
Characterization and Targeting the GDNF and Other Pathways in Salivary Stem CellsR01DE025227 · NIDCR · STANFORD UNIVERSITY · PI LE, QUYNH-THU XUAN, XIAO, NAN · 2015 to 2019
$2.0M
Targeting Galectin-1 with radiation in lung cancerR01CA161585 · NCI · STANFORD UNIVERSITY · PI KOONG, ALBERT, LE, QUYNH-THU XUAN · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA064786NCI NIH HHS R01 CA161585NIDCR NIH HHS R01 DE025227NIGMS NIH HHS R01 GM059907
6 · The paper itself

Abstract

Branching morphogenesis in the mammary gland is achieved by the migration of epithelial cells through a microenvironment consisting of stromal cells and extracellular matrix (ECM). Here we show that galectin-1 (Gal-1), an endogenous lectin that recognizes glycans bearing N-acetyllactosamine (LacNAc) epitopes, induces branching migration of mammary epithelia in vivo, ex vivo, and in 3D organotypic cultures. Surprisingly, Gal-1's effects on mammary patterning were independent of its glycan-binding ability and instead required localization within the nuclei of mammary epithelia. Nuclear translocation of Gal-1, in turn, was regulated by discrete cell-surface glycans restricted to the front of the mammary end buds. Specifically, α2,6-sialylation of terminal LacNAc residues in the end buds masked Gal-1 ligands, thereby liberating the protein for nuclear translocation. Within mammary epithelia, Gal-1 localized within nuclear Gemini bodies and drove epithelial invasiveness. Conversely, unsialylated LacNAc glycans, enriched in the epithelial ducts, sequestered Gal-1 in the extracellular environment, ultimately attenuating invasive potential. We also found that malignant breast cells possess higher levels of nuclear Gal-1 and α2,6-SA and lower levels of LacNAc than nonmalignant cells in culture and in vivo and that nuclear localization of Gal-1 promotes a transformed phenotype. Our findings suggest that differential glycosylation at the level of tissue microanatomy regulates the nuclear function of Gal-1 in the context of mammary gland morphogenesis and in cancer progression.

Indexed as

MorphogenesisAnimalsCell NucleusFemaleGalectin 1GlycosylationMammary Glands, AnimalMammary Neoplasms, AnimalMiceMice, Inbred BALB CMice, Inbred C57BLPolysaccharidesGalectin 1Polysaccharidesbreast cancergalectin-1glycobiologymammary glandsialic acid

Identifiers

PMID27496330
PMCPMC4995945
OpenAlexW2496650515

What OpenQuestion holds

Textmetadata
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.