Evidence map›Paper›PMID 35955749›Full record

ArticleInternational journal of molecular sciences2022

CD44 Contributes to the Regulation of MDR1 Protein and Doxorubicin Chemoresistance in Osteosarcoma.

Monserrat Gerardo-Ramírez, Friederike L Keggenhoff, Vanessa Giam, Diana Becker, Marco Groth, Nils Hartmann, Beate K Straub, Helen Morrison, Peter R Galle, Jens U Marquardt and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

12 authors at 2 institutions in 1 country.

Monserrat Gerardo-RamírezDepartment of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
Friederike L KeggenhoffDepartment of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
Vanessa GiamDepartment of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.ORCID 0000-0002-5453-0854
Diana BeckerDepartment of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
Marco GrothLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.ORCID 0000-0002-9199-8990
Nils HartmannInstitute of Pathology, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
Beate K StraubInstitute of Pathology, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.ORCID 0000-0002-4857-1561
Helen MorrisonLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Peter R GalleDepartment of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.ORCID 0000-0003-1967-0621
Jens U MarquardtDepartment of Medicine I, University Medical Center Schleswig-Holstein-Campus Lübeck, 23558 Lübeck, Germany.ORCID 0000-0002-8314-2682
Peter HerrlichLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Monika HartmannDepartment of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.ORCID 0000-0001-6074-6961
Johannes Gutenberg University Mainz · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DE

Funding

Deutsche Forschungsgemeinschaft HA 7860/1-2German Cancer Aid 70113491
6 · The paper itself

Abstract

Osteosarcoma is the most common type of pediatric bone tumor. Despite great advances in chemotherapy during the past decades, the survival rates of osteosarcoma patients remain unsatisfactory. Drug resistance is one of the main reasons, leading to treatment failure and poor prognosis. Previous reports correlated expression of cluster of differentiation 44 (CD44) with drug resistance and poor survival of osteosarcoma patients, however the underlying mechanisms are poorly defined. Here, we investigated the role of CD44 in the regulation of drug chemoresistance, using osteosarcoma cells isolated from mice carrying a mutation of the tumor suppressor neurofibromatosis type 2 (

Indexed as

Bone NeoplasmsOsteosarcomaAnimalsATP Binding Cassette Transporter, Subfamily B, Member 1Cell Line, TumorDoxorubicinDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansHyaluronan ReceptorsMiceTumor Suppressor Protein p53ATP Binding Cassette Transporter, Subfamily B, Member 1CD44 protein, humanDoxorubicinHyaluronan ReceptorsTumor Suppressor Protein p53bone tumorsCD44hyaluronic acidMDR1osteosarcomaproteolytic cleavage

Identifiers

PMID35955749
PMCPMC9368984
OpenAlexW4289711109

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.