Evidence map›Paper›PMID 25457412›Full record

ArticleCancer science2015

Microparticles induce multifactorial resistance through oncogenic pathways independently of cancer cell type.

Paloma Silva de Souza, André L S Cruz, João P B Viola, Raquel C Maia

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Extracellular Vesicles in Chemoresistance.Sub-cellular biochemistry · 2021
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Extracellular vesicles and blood diseases.International journal of hematology · 2017
    Review
  16. Review
  17. Membrane microparticles: shedding new light into cancer cell communication.Journal of cancer research and clinical oncology · 2016
    Review
  18. 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

4 authors at 1 institution in 1 country.

Paloma Silva de SouzaProgram of Hemato-Oncology Molecular, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
André L S Cruz
João P B Viola
Raquel C Maia
Instituto Nacional do Câncer · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidrug resistance (MDR) is considered a multifactorial event that favors cancer cells becoming resistant to several chemotherapeutic agents. Numerous mechanisms contribute to MDR, such as P-glycoprotein (Pgp/ABCB1) activity that promotes drug efflux, overexpression of inhibitors of apoptosis proteins (IAP) that contribute to evasion of apoptosis, and oncogenic pathway activation that favors cancer cell survival. MDR molecules have been identified in membrane microparticles (MP) and can be transferred to sensitive cancer cells. By co-culturing MP derived from MDR-positive cells with recipient cells, we showed that sensitive cells accumulated Pgp, IAP proteins and mRNA. In addition, MP promoted microRNA transfer and NFκB and Yb-1 activation. Therefore, our results indicate that MP can induce a multifactorial phenotype in sensitive cancer cells.

Indexed as

Drug Resistance, MultipleDrug Resistance, NeoplasmSignal TransductionAntineoplastic AgentsCarcinogenesisCell-Derived MicroparticlesCoculture TechniquesHumansK562 CellsMCF-7 CellsMicroRNAsNF-kappa BProto-Oncogene Proteins c-aktAntineoplastic AgentsMicroRNAsNF-kappa BProto-Oncogene Proteins c-aktInhibitors of apoptosis proteinsmicroparticlesmultidrug resistanceNFκBP-glycoprotein

Identifiers

PMID25457412
PMCPMC4317771
OpenAlexW2084684805

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.