Evidence map›Paper›PMID 35582577›Full record

ReviewCancer drug resistance (Alhambra, Calif.)2019

Cancer drug resistance: rationale for drug delivery systems and targeted inhibition of HSP90 family proteins.

Clélia Mathieu, Samir Messaoudi, Elias Fattal, Juliette Vergnaud-Gauduchon

Open access · diamondAbstract readReview
In one paragraph

Review in Cancer drug resistance (Alhambra, Calif.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Transcriptome reveals the role of theFrontiers in microbiology · 2023
    Article
  6. 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

4 authors at 2 institutions in 1 country.

Clélia MathieuInstitut Galien Paris-Sud, CNRS, UMR 8612, Université Paris-Sud/Paris-Saclay, Châtenay-Malabry 92296, France.
Samir MessaoudiBioCIS, CNRS, UMR 8076, Université Paris-Sud/Paris-Saclay, Châtenay-Malabry 92296, France.
Elias FattalInstitut Galien Paris-Sud, CNRS, UMR 8612, Université Paris-Sud/Paris-Saclay, Châtenay-Malabry 92296, France.
Juliette Vergnaud-GauduchonInstitut Galien Paris-Sud, CNRS, UMR 8612, Université Paris-Sud/Paris-Saclay, Châtenay-Malabry 92296, France.
Institut Galien Paris-Saclay · FRLaboratoire des Biomolécules · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanocarriers have been developed in order to protect drugs or to improve drugs efficiency by reaching the damaged tissue and avoiding systemic and local toxicity. By using HSP90 inhibitors, some cancer drug resistances have been overcome and the loading into nanocarriers of such drugs has shown an increase of their activities. This review will present some advantages of HSP90 inhibitors to treat resistant tumors; especially those targeting the mitochondrial protein TRAP1. We will also focus on the targeting of the primary tumors, cancer stem cells and metastatic cells.

Indexed as

cancerHeat-shock proteinsnanoparticlesresistance

Identifiers

PMID35582577
PMCPMC8992530
OpenAlexW2949947493

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.