Evidence map›Paper›PMID 24949434›Full record

ArticleBioMed research international2014

Gla-rich protein is a potential new vitamin K target in cancer: evidences for a direct GRP-mineral interaction.

Carla S B Viegas, Marjolein Herfs, Marta S Rafael, José L Enriquez, Alexandra Teixeira, Inês M Luís, Cynthia M R van 't Hoofd, Alexandre João, Vera L Maria, Sofia Cavaco and 5 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  4. Roles of vitamin K‑dependent protein in biomineralization (Review).International journal of molecular medicine · 2024
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  7. Article
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  12. Vitamin K Dependent Proteins in Kidney Disease.International journal of molecular sciences · 2019
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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

15 authors at 6 institutions in 2 countries.

Carla S B ViegasCentre of Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal ; GenoGla Diagnostics, Centre of Marine Sciences (CCMAR), University of Algarve, 8005-139 Faro, Portugal.
Marjolein HerfsVitaK, Maastricht University, 6229 EV Maastricht, The Netherlands.
Marta S RafaelCentre of Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal.
José L EnriquezAlgarve Medical Centre, Department of Histopathology, 8000-386 Faro, Portugal.
Alexandra TeixeiraAlgarve Medical Centre, Department of Histopathology, 8000-386 Faro, Portugal.
Inês M LuísCentre of Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal.
Cynthia M R van 't HoofdVitaK, Maastricht University, 6229 EV Maastricht, The Netherlands.
Alexandre JoãoLisbon Central Hospital-CHLC, Department of Dermatology, 1169-050 Lisbon, Portugal.
Vera L MariaAdministração Regional de Saúde do Algarve, 8135-014 Faro, Portugal.
Sofia CavacoCentre of Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal.
Ana FerreiraLisbon Central Hospital-CHLC, Department of Dermatology, 1169-050 Lisbon, Portugal.
Manuel SerraPrivate Hospitals of Portugal, HPP-Santa Maria Hospital, 8000-140 Faro, Portugal.
Elke TheuwissenVitaK, Maastricht University, 6229 EV Maastricht, The Netherlands.
Cees VermeerVitaK, Maastricht University, 6229 EV Maastricht, The Netherlands.
Dina C SimesCentre of Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal ; GenoGla Diagnostics, Centre of Marine Sciences (CCMAR), University of Algarve, 8005-139 Faro, Portugal.
University of Algarve · PTMaastricht University · NLAlgarve Biomedical Center · PTCentro Hospitalar de Lisboa Central · PTAdministração Regional de Saúde de Lisboa e Vale do Tejo · PTHospital de Santa Maria · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gla-rich protein (GRP) was described in sturgeon as a new vitamin-K-dependent protein (VKDP) with a high density of Gla residues and associated with ectopic calcifications in humans. Although VKDPs function has been related with γ-carboxylation, the Gla status of GRP in humans is still unknown. Here, we investigated the expression of recently identified GRP spliced transcripts, the γ-carboxylation status, and its association with ectopic calcifications, in skin basal cell and breast carcinomas. GRP-F1 was identified as the predominant splice variant expressed in healthy and cancer tissues. Patterns of γ-carboxylated GRP (cGRP)/undercarboxylated GRP (ucGRP) accumulation in healthy and cancer tissues were determined by immunohistochemistry, using newly developed conformation-specific antibodies. Both GRP protein forms were found colocalized in healthy tissues, while ucGRP was the predominant form associated with tumor cells. Both cGRP and ucGRP found at sites of microcalcifications were shown to have in vitro calcium mineral-binding capacity. The decreased levels of cGRP and predominance of ucGRP in tumor cells suggest that GRP may represent a new target for the anticancer potential of vitamin K. Also, the direct interaction of cGRP and ucGRP with BCP crystals provides a possible mechanism explaining GRP association with pathological mineralization.

Indexed as

Calcinosisalpha-GalactosidaseBasal Cell CarcinomaBreast NeoplasmsFemaleHumansNaphthoquinonesOsteocalcinSkin NeoplasmsVitamin Kalpha-GalactosidaseGLA protein, humanNaphthoquinonesOsteocalcinVitamin K

Identifiers

PMID24949434
PMCPMC4052551
OpenAlexW2102690235

What OpenQuestion holds

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LicenceCC BY
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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.