Evidence map›Paper›PMID 33203838›Full record

ArticleCell death & disease2020

GARP promotes the proliferation and therapeutic resistance of bone sarcoma cancer cells through the activation of TGF-β.

Ana Belén Carrillo-Gálvez, Juan Esteban Quintero, René Rodríguez, Sofía T Menéndez, M Victoria González, Verónica Blanco-Lorenzo, Eva Allonca, Virgínea de Araújo Farias, Juan Elías González-Correa, Nadina Erill-Sagalés and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. World journal of gastroenterology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Selective activation of TGFβ signaling byAmerican journal of cancer research · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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

18 authors at 9 institutions in 3 countries.

Ana Belén Carrillo-GálvezCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain. anacarrillo@ugr.es.
Juan Esteban QuinteroCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain.
René RodríguezInstituto de Investigación Sanitaria del Principado de Asturias, Hospital Universitario Central de Asturias, Avenida de Roma, s/n, 33011, Oviedo, Spain.
Sofía T MenéndezInstituto de Investigación Sanitaria del Principado de Asturias, Hospital Universitario Central de Asturias, Avenida de Roma, s/n, 33011, Oviedo, Spain.
M Victoria GonzálezInstituto de Investigación Sanitaria del Principado de Asturias, Hospital Universitario Central de Asturias, Avenida de Roma, s/n, 33011, Oviedo, Spain.
Verónica Blanco-LorenzoInstituto de Investigación Sanitaria del Principado de Asturias, Hospital Universitario Central de Asturias, Avenida de Roma, s/n, 33011, Oviedo, Spain.
Eva AlloncaInstituto de Investigación Sanitaria del Principado de Asturias, Hospital Universitario Central de Asturias, Avenida de Roma, s/n, 33011, Oviedo, Spain.
Virgínea de Araújo FariasDepartment of Neurosurgery, Mayo Clinic, Jacksonville, FL, 32224, USA.
Juan Elías González-CorreaCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain.
Nadina Erill-SagalésATRYS, Carrer Provença 392 PB, 08025, Barcelona, Spain.
Iñigo Martínez-ZubiaurreDepartment of Clinical Medicine, Faculty of Health Sciences, UiT-The Arctic University of Norway, 9037, Tromsø, Norway.
Turid HellevikUniversity Hospital of Northern Norway, 9038, Tromsø, Norway.
Sabina Sánchez-HernándezCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain.
Pilar MuñozCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain.
Federico ZuritaDepartamento de Genética e Instituto de Biotecnología, Centro de Investigación Biomédica. Universidad de Granada, Granada, Spain.
Francisco MartínCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain.
Juan Carlos Rodríguez-ManzanequeCentre for Genomics and Oncological Research (GENYO), PTS Granada, Avenida de la Ilustración 114, 18016, Granada, Spain.ORCID 0000-0001-5951-7029
Per AndersonServicio de Análisis Clínicos e Inmunología, UGC Laboratorio Clínico, Hospital Universitario Virgen de las Nieves, Av. de las Fuerzas Armadas 2, Granada, 18014, Spain. per.anderson@ibsGRANADA.es.
Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ESCentro de Investigación Biomédica en Red de Cáncer · ESHospital Universitario Central de Asturias · ESInstituto de Investigación Biosanitaria de Granada · ESMayo Clinic in Florida · USUiT The Arctic University of Norway · NOUniversidad de Granada · ESUniversidad de Oviedo · ESUniversity Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcomas are mesenchymal cancers with poor prognosis, representing about 20% of all solid malignancies in children, adolescents, and young adults. Radio- and chemoresistance are common features of sarcomas warranting the search for novel prognostic and predictive markers. GARP/LRRC32 is a TGF-β-activating protein that promotes immune escape and dissemination in various cancers. However, if GARP affects the tumorigenicity and treatment resistance of sarcomas is not known. We show that GARP is expressed by human osteo-, chondro-, and undifferentiated pleomorphic sarcomas and is associated with a significantly worse clinical prognosis. Silencing of GARP in bone sarcoma cell lines blocked their proliferation and induced apoptosis. In contrast, overexpression of GARP promoted their growth in vitro and in vivo and increased their resistance to DNA damage and cell death induced by etoposide, doxorubicin, and irradiation. Our data suggest that GARP could serve as a marker with therapeutic, prognostic, and predictive value in sarcoma. We propose that targeting GARP in bone sarcomas could reduce tumour burden while simultaneously improving the efficacy of chemo- and radiotherapy.

Indexed as

AdolescentAdultAgedAged, 80 and overAnimalsBone NeoplasmsCell Line, TumorCell ProliferationChildChild, PreschoolFemaleHeterograftsHumansMaleMembrane ProteinsMiceLRRC32 protein, humanMembrane ProteinsTransforming Growth Factor beta

Identifiers

PMID33203838
PMCPMC7673987
OpenAlexW3103948909

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.