Evidence map›Paper›PMID 20074598›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2010

Effects of pluronic and doxorubicin on drug uptake, cellular metabolism, apoptosis and tumor inhibition in animal models of MDR cancers.

Elena V Batrakova, Shu Li, Anna M Brynskikh, Amit K Sharma, Yili Li, Michael Boska, Nan Gong, R Lee Mosley, Valery Yu Alakhov, Howard E Gendelman and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 156 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Drug delivery carriers with therapeutic functions.Advanced drug delivery reviews · 2021
    Review
  7. Article
  8. Macrophage-Derived Extracellular Vesicles as Drug Delivery Systems for Triple Negative Breast Cancer (TNBC) Therapy.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Neurotheranostics as personalized medicines.Advanced drug delivery reviews · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Development of exosome-encapsulated paclitaxel to overcome MDR in cancer cells.Nanomedicine : nanotechnology, biology, and medicine · 2016
    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

11 authors at 3 institutions in 2 countries.

Elena V BatrakovaCollege of Pharmacy, Department of Pharmaceutical Sciences, 985830 Nebraska Medical Center, Omaha, NE 68198-5830, USA.
Shu Li
Anna M Brynskikh
Amit K Sharma
Yili Li
Michael Boska
Nan Gong
R Lee Mosley
Valery Yu Alakhov
Howard E Gendelman
Alexander V Kabanov
Nebraska Medical Center · USUniversity of Nebraska Medical Center · USSupratek Pharma (Canada) · CA

Funding

TARGETED NANOCARRIER FOR SIRNA DELIVERY TO TUMOR VASCULATUREP20RR021937 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KABANOV, ALEXANDER V · 2008 to 2011
$8.6M
Pluronic Block Copolymers in Drug Resistant CancerR01CA089225 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KABANOV, ALEXANDER V · 2001 to 2011
$2.2M
T Cell-Mediated Neurodegeneration in Parkinson's DiseaseR01NS070190 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI MOSLEY, R LEE · 2010 to 2014
$1.8M
NCI NIH HHS CA89225NCI NIH HHS R01 CA089225NCRR NIH HHS P20 RR021937NCRR NIH HHS RR021937NINDS NIH HHS R01 NS070190
6 · The paper itself

Abstract

Cancer chemotherapy is believed to be impeded by multidrug resistance (MDR). Pluronic (triblock copolymers of poly(ethylene oxide) (PEO) and poly(propylene oxide) (PPO), PEO-b-PPO-b-PEO) were previously shown to sensitize MDR tumors to antineoplastic agents. This study uses animal models of Lewis lung carcinoma (3LL-M27) and T-lymphocytic leukemia (P388/ADR and P388) derived solid tumors to delineate mechanisms of sensitization of MDR tumors by Pluronic P85 (P85) in vivo. First, non-invasive single photon emission computed tomography (SPECT) and tumor tissue radioactivity sampling demonstrate that intravenous co-administration of P85 with a Pgp substrate, 99Tc-sestamibi, greatly increases the tumor uptake of this substrate in the MDR tumors. Second, 31P magnetic resonance spectroscopy (31P-MRS) in live animals and tumor tissue sampling for ATP suggest that P85 and doxorubicin (Dox) formulations induce pronounced ATP depletion in MDR tumors. Third, these formulations are shown to increase tumor apoptosis in vivo by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay and reverse transcription polymerase chain reaction (RT-PCR) for caspases 8 and 9. Altogether, formulation of Dox with P85 results in increased inhibition of the growth solid tumors in mice and represents novel and promising strategy for therapy of drug resistant cancers.

Indexed as

Adenosine TriphosphateAnimalsApoptosisBody WeightCarcinoma, Lewis LungCell Line, TumorDoxorubicinDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansLeukemia, T-CellMiceMice, Inbred C57BLPoloxamerTomography, Emission-Computed, Single-PhotonAdenosine TriphosphateDoxorubicinPoloxamer

Identifiers

PMID20074598
PMCPMC3089980
OpenAlexW1990017773

What OpenQuestion holds

Textmetadata
LicenceTDM
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.