Evidence map›Paper›PMID 30856208›Full record

Trial reportPloS one2019

Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients.

Nina Gran Egeland, Marie Austdal, Bianca van Diermen-Hidle, Emma Rewcastle, Einar G Gudlaugsson, Jan P A Baak, Ivar Skaland, Emiel A M Janssen, Kristin Jonsdottir

Open access · goldAbstract readClinical TrialMulticenter StudyValidation Study
In one paragraph

Trial report in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Dendritic Cell-Associated MARCKSL1 Regulates Fibroblast Differentiation During Wound Healing.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

9 authors at 1 institution in 1 country.

Nina Gran EgelandDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Marie AustdalDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Bianca van Diermen-HidleDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Emma RewcastleDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Einar G GudlaugssonDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Jan P A BaakDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Ivar SkalandDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Emiel A M JanssenDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.
Kristin JonsdottirDepartment of Pathology, Stavanger University Hospital, Stavanger, Norway.ORCID 0000-0001-9772-925X
Stavanger University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein expression of Myristoylated alanine-rich C kinase substrate like-1 (MARCKSL1) has been identified as a prognostic factor in lymph-node negative (LN-) breast cancer patients. We aim to validate MARCKSL1 protein expression as a prognostic marker for distant metastasis-free survival (DMFS) in a new cohort of LN- breast cancer patients. MARCKSL1 expression was evaluated in 151 operable T1,2N0M0 LN- breast cancer patients by immunohistochemistry. Median follow-up time was 152 months, range 11-189 months. Results were compared with classical prognosticators (age, tumor diameter, grade, estrogen receptor, and proliferation) using single (Kaplan-Meier) and multivariate (Cox model) survival analysis. Thirteen patients (9%) developed distant metastases. With both single and multiple analysis of all features, MARCKSL1 did not show a significant prognostic value for DMFS (p = 0.498). Of the assessed classical prognosticators, only tumor diameter showed prognostic value (hazard ratio 9.3, 95% confidence interval 2.8-31.0, p <0.001). MARCKSL1 expression could not be confirmed as a prognostic factor in this cohort. Possible reasons include changes in diagnostic and treatment guidelines between the discovery and validation cohorts. Further studies are needed to reveal the potential biological role of this protein in breast cancer.

Indexed as

AdultAgedBiomarkers, TumorBreast NeoplasmsCalmodulin-Binding ProteinsDisease-Free SurvivalFemaleFollow-Up StudiesHumansLymph NodesMembrane ProteinsMicrofilament ProteinsMiddle AgedNeoplasm ProteinsSurvival RateBiomarkers, TumorCalmodulin-Binding ProteinsMARCKSL1 protein, humanMembrane ProteinsMicrofilament ProteinsNeoplasm Proteins

Identifiers

PMID30856208
PMCPMC6411117
OpenAlexW2921186868

What OpenQuestion holds

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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.