Evidence map›Paper›PMID 28187434›Full record

ArticleOncotarget2017

Interface between breast cancer cells and the tumor microenvironment using platelet-rich plasma to promote tumor angiogenesis - influence of platelets and fibrin bundles on the behavior of breast tumor cells.

Sheila Siqueira Andrade, Joana Tomomi Sumikawa, Eloísa Dognani Castro, Fabricio Pereira Batista, Edgar Paredes-Gamero, Lilian Carolina Oliveira, Izabel Monastério Guerra, Giovani Bravin Peres, Renan Pelluzzi Cavalheiro, Luiz Juliano and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Platelet-Rich Plasma Inhibits Breast Cancer Proliferation.Clinical Medicine Insights. Oncology · 2024
    Article
  5. An Insight into Recent Advances on Platelet Function in Health and Disease.International journal of molecular sciences · 2022
    Review
  6. Prognostic implications of NScientific reports · 2022
    Article
  7. Reviewing cancer's biology: an eclectic approach.Journal of the Egyptian National Cancer Institute · 2021
    Review
  8. Review
  9. Breast tumor-on-chip models: From disease modeling to personalized drug screening.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
  10. Review
  11. Article
  12. Biotech-Educated Platelets: Beyond Tissue Regeneration 2.0.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Observational
  19. Tissue engineering and regenerative medicine · 2018
    Article
  20. 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

15 authors at 2 institutions in 1 country.

Sheila Siqueira AndradeDepartment of Gynecology of The Federal University of São Paulo, Brazil.
Joana Tomomi SumikawaDepartment of Gynecology of The Federal University of São Paulo, Brazil.
Eloísa Dognani CastroDepartment of Biochemistry of The Federal University of São Paulo, Brazil.
Fabricio Pereira BatistaDepartment of Biochemistry of The Federal University of São Paulo, Brazil.
Edgar Paredes-GameroDepartment of Biochemistry of The Federal University of São Paulo, Brazil.
Lilian Carolina OliveiraDepartment of Biophysics of The Federal University of São Paulo, Brazil.
Izabel Monastério GuerraDepartment of Gynecology of The Federal University of São Paulo, Brazil.
Giovani Bravin PeresDepartment of Biochemistry of The Federal University of São Paulo, Brazil.
Renan Pelluzzi CavalheiroDepartment of Biochemistry of The Federal University of São Paulo, Brazil.
Luiz JulianoDepartment of Biophysics of The Federal University of São Paulo, Brazil.
Afonso Pinto NazárioDepartment of Gynecology of The Federal University of São Paulo, Brazil.
Gil FacinaDepartment of Gynecology of The Federal University of São Paulo, Brazil.
Siu Mui TsaiCell and Molecular Biology Laboratory, Center for Nuclear Energy in Agriculture CENA, University of São Paulo USP, Piracicaba, SP, Brazil.
Maria Luiza Vilela OlivaDepartment of Biochemistry of The Federal University of São Paulo, Brazil.
Manoel João Batista Castello GirãoDepartment of Gynecology of The Federal University of São Paulo, Brazil.
Universidade Federal de São Paulo · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer progression is associated with an evolving tissue interface of direct epithelial-tumor microenvironment interactions. In biopsies of human breast tumors, extensive alterations in molecular pathways are correlated with cancer staging on both sides of the tumor-stroma interface. These interactions provide a pivotal paracrine signaling to induce malignant phenotype transition, the epithelial-mesenchymal transition (EMT). We explored how the direct contact between platelets-fibrin bundles primes metastasis using platelet-rich plasma (PRP) as a source of growth factors and mimics the provisional fibrin matrix between actively growing breast cancer cells and the tumor stroma. We have demonstrated PRP functions, modulating cell proliferation that is tumor-subtype and cancer cell-type-specific. Epithelial and stromal primary cells were prepared from breast cancer biopsies from 21 women with different cancer subtypes. Cells supplemented with PRP were immunoblotted with anti-phospho and total Src-Tyr-416, FAK-Try-925, E-cadherin, N-cadherin, TGF-β, Smad2, and Snail monoclonal antibodies. Breast tumor cells from luminal B and HER2 subtypes showed the most malignant profiles and the expression of thrombin and other classes of proteases at levels that were detectable through FRET peptide libraries. The angiogenesis process was investigated in the interface obtained between platelet-fibrin-breast tumor cells co-cultured with HUVEC cells. Luminal B and HER2 cells showed robust endothelial cell capillary-like tubes ex vivo. The studied interface contributes to the attachment of endothelial cells, provides a source of growth factors, and is a solid substrate. Thus, replacement of FBS supplementation with PRP supplementation represents an efficient and simple approach for mimicking the real multifactorial tumor microenvironment.

Indexed as

Blood PlateletsBreast NeoplasmsDisease ProgressionEpithelial CellsFemaleFibrinHumansHuman Umbilical Vein Endothelial CellsNeovascularization, PathologicPlatelet-Rich PlasmaStromal CellsTumor MicroenvironmentFibrinbreast cancercancerplatelet-rich plasmaplateletstumor microenvironment

Identifiers

PMID28187434
PMCPMC5370006
OpenAlexW2586263396

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.