Evidence map›Paper›PMID 12682633›Full record

ArticleLeukemia2003

Upregulation of galectin-7 in murine lymphoma cells is associated with progression toward an aggressive phenotype.

S Moisan, M Demers, J Mercier, T Magnaldo, E F Potworowski, Y St-Pierre

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Galectin-7 in Epithelial Homeostasis and Carcinomas.International journal of molecular sciences · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

6 authors.

S MoisanINRS-Institut Armand-Frappier, University of uébec, Laval, Canada.
M Demers
J Mercier
T Magnaldo
E F Potworowski
Y St-Pierre

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously shown that ICAM-1-deficient mice were resistant to lymphoma dissemination of intravenously injected 164T2 lymphoma cells. Highly aggressive variants of this cell line, however, could overcome this resistance. To discern the complex pattern of gene expression involved in the evolution of aggressiveness in lymphoma cells, we compared the transcriptome of 164T2 cells with that of their aggressive variants using cDNA arrays. We identified several genes that were differentially expressed in nonmetastatic lymphoma cells and their metastatic variants. Galectin-7, associated with the development of chemically induced mammary carcinoma, was one such gene whose expression was significantly upregulated. We showed that it was constitutively expressed in aggressive variants, at both mRNA and protein levels. Galectin-7 expression in aggressive lymphoma cells was induced upon in vivo selection in several organs, including the thymus, the spleen and kidneys. We also showed that treatment of nonaggressive lymphoma cells with 5-aza-2'-deoxycytidine was sufficient to induce galectin-7 gene expression. This report is the first to show that galectin-7 is expressed in aggressive lymphoma.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntimetabolites, AntineoplasticAzacitidineDecitabineDisease ProgressionFemaleGalectinsGene Expression ProfilingLymphoma, T-CellMaleMiceMice, Inbred C57BLNeoplasm MetastasisNeoplasm ProteinsNeoplasms, Radiation-InducedAntimetabolites, AntineoplasticAzacitidineDecitabineGalectinsLgals7 protein, mouseNeoplasm ProteinsRNA, MessengerRNA, Neoplasm

Identifiers

PMID12682633

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.