Evidence map›Paper›PMID 25259711›Full record

ArticlePloS one2014

Galectin expression profiling identifies galectin-1 and Galectin-9Δ5 as prognostic factors in stage I/II non-small cell lung cancer.

Iris A Schulkens, Roy Heusschen, Vivian van den Boogaart, Robert-Jan van Suylen, Anne-Marie C Dingemans, Arjan W Griffioen, Victor L Thijssen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  8. Tim-3 finds its place in the cancer immunotherapy landscape.Journal for immunotherapy of cancer · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Role of galectins in lung cancer.Oncology letters · 2017
    Article
  14. Article
  15. Review
  16. Review
  17. Article
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

7 authors at 2 institutions in 1 country.

Iris A SchulkensAngiogenesis Laboratory, Department of Medical Oncology, VU University medical center, Amsterdam, The Netherlands.
Roy HeusschenAngiogenesis Laboratory, Department of Medical Oncology, VU University medical center, Amsterdam, The Netherlands.
Vivian van den BoogaartDepartment of Pulmonology, Maastricht University medical center, Maastricht, The Netherlands; GROW - School for oncology and developmental biology, Maastricht University medical center, Maastricht, The Netherlands.
Robert-Jan van SuylenDepartment of Pathology, Maastricht University medical center, Maastricht, The Netherlands.
Anne-Marie C DingemansDepartment of Pulmonology, Maastricht University medical center, Maastricht, The Netherlands; GROW - School for oncology and developmental biology, Maastricht University medical center, Maastricht, The Netherlands.
Arjan W GriffioenAngiogenesis Laboratory, Department of Medical Oncology, VU University medical center, Amsterdam, The Netherlands.
Victor L ThijssenAngiogenesis Laboratory, Department of Medical Oncology, VU University medical center, Amsterdam, The Netherlands; Department of Radiotherapy, VU University medical center, Amsterdam, The Netherlands.
Amsterdam UMC Location VUmc · NLMaastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately 30-40% of the patients with early stage non-small cell lung cancer (NSCLC) will present with recurrent disease within two years of resection. Here, we performed extensive galectin expression profiling in a retrospective study using frozen and paraffin embedded tumor tissues from 87 stage I/II NSCLC patients. Our data show that galectin mRNA expression in NSCLC is confined to galectin-1, -3, -4, -7, -8, and -9. Next to stage, univariable Cox regression analysis identified galectin-1, galectin-9FL and galectin-9Δ5 as possible prognostic markers. Kaplan-Meier survival estimates revealed that overall survival was significantly shorter in patients that express galectin-1 above median levels, i.e., 23.0 (2.9-43.1) vs. 59.9 (47.7-72.1) months (p = 0.020) as well as in patients that express galectin-9Δ5 or galectin-9FL below the median, resp. 59.9 (41.9-75.9) vs. 32.8 (8.7-56.9) months (p = 0.014) or 23.2 (-0.4-46.8) vs. 58.9 (42.9-74.9) months (p = 0.042). All three galectins were also prognostic for disease free survival. Multivariable Cox regression analysis showed that for OS, the most significant prognostic model included stage, age, gal-1 and gal-9Δ5 while the model for DFS included stage, age and gal-9Δ5. In conclusion, the current study confirms the prognostic value of galectin-1 and identifies galectin-9Δ5 as novel potential prognostic markers in early stage NSCLC. These findings could help to identify early stage NSCLC patients that might benefit most from adjuvant chemotherapy.

Indexed as

Gene Expression ProfilingCarcinoma, Non-Small-Cell LungCell Line, TumorFemaleGalectin 1GalectinsGene ExpressionHumansLung NeoplasmsMaleNeoplasm StagingPrognosisRetrospective StudiesRisk FactorsRNA, MessengerGalectin 1GalectinsLGALS9 protein, humanRNA, Messenger

Identifiers

PMID25259711
PMCPMC4178059
OpenAlexW2044785206

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.