Evidence map›Paper›PMID 24657939›Full record

ReviewSeminars in cancer biology2014

Nuclear transport of galectin-3 and its therapeutic implications.

Tatsuyoshi Funasaka, Avraham Raz, Pratima Nangia-Makker

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
2.8field-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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
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  19. Examining Galectin Gene Regulation by Reporter Assays.Methods in molecular biology (Clifton, N.J.) · 2022
    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

3 authors at 2 institutions in 1 country.

Tatsuyoshi FunasakaNanzando Pharmacies Co., Takanawa, Minato-ku, Tokyo 108-0074, Japan.
Avraham RazDepartment of Oncology, School of Medicine, Wayne State University, United States.
Pratima Nangia-MakkerDepartment of Internal Medicine, School of Medicine, Wayne State University, United States; John D. Dingell V.A. Medical Center, Detroit, MI 48201, United States. Electronic address: makkerp@med.wayne.edu.
John D. Dingell VA Medical Center · USWayne State University · US

Funding

The Role of Tumor Cell Surface Lectin in MetastasesR37CA046120 · NCI · WAYNE STATE UNIVERSITY · PI RAZ, AVRAHAM · 2007 to 2014
$3.0M
NCI NIH HHS R37 CA046120NCI NIH HHS R37CA46120
6 · The paper itself

Abstract

Galectin-3, a member of β-galactoside-binding gene family is a multi-functional protein, which regulates pleiotropic biological functions such as cell growth, cell adhesion, cell-cell interactions, apoptosis, angiogenesis and mRNA processing. Its unique structure enables it to interact with a plethora of ligands in a carbohydrate dependent or independent manner. Galectin-3 is mainly a cytosolic protein, but can easily traverse the intracellular and plasma membranes to translocate into the nucleus, mitochondria or get externalized. Depending on the cell type, specific experimental conditions in vitro, cancer type and stage, galectin-3 has been reported to be exclusively cytoplasmic, predominantly nuclear or distributed between the two compartments. In this review we have summarized the dynamics of galectin-3 shuttling between the nucleus and the cytoplasm, the nuclear transport mechanisms of galectin-3, how its specific interactions with the members of β-catenin signaling pathways affect tumor progression, and its implications as a therapeutic target.

Indexed as

Active Transport, Cell NucleusAnimalsGalectin 3HumansMolecular Targeted TherapyNeoplasmsNuclear Pore Complex ProteinsNucleocytoplasmic Transport ProteinsSignal TransductionGalectin 3Nuclear Pore Complex ProteinsNucleocytoplasmic Transport ProteinsBeta cateninGalectin-3Nuclear cytoplasmic transport

Identifiers

PMID24657939
PMCPMC4108496
OpenAlexW1992596514

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.