Evidence map›Paper›PMID 24867421›Full record

ArticlePharmaceutical research2014

EphA2 targeting pegylated nanocarrier drug delivery system for treatment of lung cancer.

Apurva R Patel, Mahavir Chougule, Mandip Singh

Open access · greenAbstract read
In one paragraph

Article in Pharmaceutical research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. EphA2 in Cancer: Molecular Complexity and Therapeutic Opportunities.International journal of molecular sciences · 2024
    Review
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  15. Inhalable oridonin-loaded poly(lactic-Acta pharmaceutica Sinica. B · 2017
    Article
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  20. Treatment of Dutch rat models of glioma using EphrinA1-PE38/GM-CSF chitosan nanoparticles by in situ activation of dendritic cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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

3 authors at 2 institutions in 1 country.

Apurva R PatelCollege of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, Florida, 32307, USA.
Mahavir Chougule
Mandip Singh
Florida Agricultural and Mechanical University · USUniversity of Hawaii at Hilo · US

Funding

Targeted Nanocarrier Combination Based Therapy for Lung CancerP20MD006738 · NIMHD · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI RAHMAN, SALEH MD. MAHMUDUR · 2012 to 2016
$5.6M
Targeted Nanocarriers for Treatment of Lung CancerSC1CA161676 · NCI · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI SACHDEVA, MANDIP SINGH · 2011 to 2014
$1.1M
Role of Telmisartan on Intra-Tumoral Distribution of Targeted NanoparticlesR21CA175618 · NCI · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI SACHDEVA, MANDIP SINGH · 2014 to 2015
$341k
NCI NIH HHS R21 CA175618NCI NIH HHS SC1 CA161676NIMHD NIH HHS P20 MD006738
6 · The paper itself

Abstract

purposeEvaluation of tumor targeting pegylated EphA2 peptide coated nanoparticles (ENDDs) of a novel anticancer agent DIM-C-pPhC6H5 (DIM-P) and Docetaxel (DOC) and investigate its antitumor activity and potential for treatment of lung cancer.

methodsNanoparticles were prepared with DIM-P and DOC (NDDs) using Nano-DeBEE. ENDDs were prepared by conjugating NDDs with 6His-PEG2K-EphA2 peptide and characterized for physicochemical properties, binding assay, cytotoxicity, cellular uptake studies, drug release and pharmacokinetic parameters. Anti-tumor activity of ENDDs was evaluated using a metastatic H1650 and orthotopic A549 tumor models in nude mice and tumor tissue were analyzed by RT-PCR and immunohistochemistry.

resultsParticle size and entrapment efficiency of ENDDs were 197 ± 21 nm and 95 ± 2%. ENDDs showed 32.5 ± 3.5% more cellular uptake than NDDs in tumor cells. ENDDs showed 23 ± 3% and 26 ± 4% more tumor reduction compared to NDDs in metastatic and orthotopic tumor models, respectively. In-vivo imaging studies using the Care stream MX FX Pro system showed (p < 0.001) 40-60 fold higher flux for ENDDs compared to NDDs at tumor site.

conclusionsThe results emanating from these studies demonstrate anti-cancer potential of DIM-P and the role of ENDDs as effective tumor targeting drug delivery systems for lung cancer treatment.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell SurvivalDrug CarriersEndocytosisHumansIndolesLigandsLung NeoplasmsMice, Inbred BALB CMice, NudeMolecular Targeted TherapyNanoparticlesPolyethylene GlycolsPPAR gamma1,1-bis(3'-indolyl)-1-(4-biphenyl)methaneAntineoplastic AgentsDrug CarriersIndolesLigandsPolyethylene GlycolsPPAR gammaReceptor, EphA2

Identifiers

PMID24867421
PMCPMC5725227
OpenAlexW2001547191

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.