Evidence map›Paper›PMID 25860932›Full record

ArticleOncotarget2015

Controlled release microspheres loaded with BMP7 suppress primary tumors from human glioblastoma.

Pilar González-Gómez, Jose Crecente-Campo, Cristina Zahonero, Maria de la Fuente, Aurelio Hernández-Laín, Helena Mira, Pilar Sánchez-Gómez, Marcos Garcia-Fuentes

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

8 authors at 6 institutions in 1 country.

Pilar González-GómezUFIEC, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Jose Crecente-CampoCenter for Research in Molecular Medicine and Chronic Diseases (CIMUS), Department of Pharmacy and Pharmaceutical Technology, and Health Research Institute (IDIS), Universidad de Santiago de Compostela, Santiago de Compostela, A Coruña, Spain.
Cristina ZahoneroUFIEC, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Maria de la FuenteNano-Oncologicals Laboratory, Translational Medical Oncology, Clinical University Hospital and Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
Aurelio Hernández-LaínUnidad Multidisciplinar de Neurooncología, Hospital Universitario 12 de Octubre, Madrid, Spain.
Helena MiraUFIEC, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Pilar Sánchez-GómezUFIEC, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Marcos Garcia-FuentesCenter for Research in Molecular Medicine and Chronic Diseases (CIMUS), Department of Pharmacy and Pharmaceutical Technology, and Health Research Institute (IDIS), Universidad de Santiago de Compostela, Santiago de Compostela, A Coruña, Spain.
Unidad Funcional de Investigación de Enfermedades Crónicas · ESCenter for Research in Molecular Medicine and Chronic Diseases · ESHospital Universitario 12 De Octubre · ESInstituto de Investigación Sanitaria de Santiago · ESInstituto de Salud Carlos III · ESUniversidade de Santiago de Compostela · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma tumor initiating cells are believed to be the main drivers behind tumor recurrence, and therefore therapies that specifically manage this population are of great medical interest. In a previous work, we synthesized controlled release microspheres optimized for intracranial delivery of BMP7, and showed that these devices are able to stop the in vitro growth of a glioma cell line. Towards the translational development of this technology, we now explore these microspheres in further detail and characterize the mechanism of action and the in vivo therapeutic potential using tumor models relevant for the clinical setting: human primary glioblastoma cell lines. Our results show that BMP7 can stop the proliferation and block the self-renewal capacity of those primary cell lines that express the receptor BMPR1B. BMP7 was encapsulated in poly (lactic-co-glycolic acid) microspheres in the form of a complex with heparin and Tetronic, and the formulation provided effective release for several weeks, a process controlled by carrier degradation. Data from xenografts confirmed reduced and delayed tumor formation for animals treated with BMP7-loaded microspheres. This effect was coincident with the activation of the canonical BMP signaling pathway. Importantly, tumors treated with BMP7-loaded microspheres also showed downregulation of several markers that may be related to a malignant stem cell-like phenotype: CD133(+), Olig2, and GFAPδ. We also observed that tumors treated with BMP7-loaded microspheres showed enhanced expression of cell cycle inhibitors and reduced expression of the proliferation marker PCNA. In summary, BMP7-loaded controlled release microspheres are able to inhibit GBM growth and reduce malignancy markers. We envisage that this kind of selective therapy for tumor initiating cells could have a synergistic effect in combination with conventional cytoreductive therapy (chemo-, radiotherapy) or with immunotherapy.

Indexed as

ApoptosisMicrospheresAnimalsBlotting, WesternBone Morphogenetic Protein 7Brain NeoplasmsCell MovementCell ProliferationDelayed-Action PreparationsGlioblastomaHumansImmunoenzyme TechniquesMiceMice, NudeReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionBMP7 protein, humanBone Morphogenetic Protein 7Delayed-Action PreparationsRNA, Messengerbone morphogenetic proteincontrolled releaseglioblastomamicrospherestumor initiating cells

Identifiers

PMID25860932
PMCPMC4484431
OpenAlexW1886820080

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.